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ANIX:Segment
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM 10-Q
☒
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended January 31, 2025
or
☐ TRANSITION REPORT PURSUANT TO SECTION 13
OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from ______ to ______
Commission file number 001-37492
ANIXA BIOSCIENCES,
INC.
(Exact name of registrant as specified in its charter)
Delaware |
|
11-2622630 |
(State or other jurisdiction of |
|
(I.R.S. Employer |
incorporation or organization) |
|
Identification No.) |
3150 Almaden Expressway, Suite 250 |
|
|
San Jose, CA |
|
95118 |
(Address of principal executive offices) |
|
(Zip Code) |
(408) 708-9808
(Registrant’s telephone number, including area
code)
Securities registered pursuant to Section 12(b) of
the Act:
Title of each class |
|
Trading symbol |
|
Name of exchange on which registered |
Common Stock, par value $.01 per share |
|
ANIX |
|
NASDAQ Capital Market |
Indicate by check mark whether the registrant: (1)
has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months
(or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements
for the past 90 days.
Indicate by check mark whether the registrant has
submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of
this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).
Indicate by check mark whether the registrant is a
large accelerated filer, an accelerated filer, a non-accelerated filer, smaller reporting company, or an emerging growth company. See
the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and
“emerging growth company” in Rule 12b-2 of the Exchange Act.
|
Large accelerated filer ☐ |
|
|
|
Accelerated filer ☐ |
|
Non-accelerated filer ☒ |
|
Smaller reporting company ☒ |
|
Emerging growth company ☐ |
If an emerging growth company, indicate by check mark
if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards
provided pursuant to Section 13(a) of the Exchange Act. ☐
Indicate by check mark whether the registrant is a
shell company (as defined in Rule 12b-2 of the Exchange Act).
Indicate the number of shares outstanding of each
of the issuer’s classes of common stock, as of the latest practicable date.
On March 11, 2025 the registrant had outstanding
32,196,862 shares of Common Stock, par value $.01 per share, which is the registrant’s only class of common stock.
TABLE OF CONTENTS
PART I. FINANCIAL INFORMATION
Item 1. Financial
Statements.
ANIXA BIOSCIENCES,
INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED BALANCE SHEETS (UNAUDITED)
(in thousands, except share and per share data)
| |
January 31, 2025 | | |
October 31, 2024 | |
ASSETS | |
| | | |
| | |
Current assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 1,053 | | |
$ | 1,271 | |
Short-term investments | |
| 16,202 | | |
| 18,653 | |
Receivables | |
| - | | |
| 173 | |
Prepaid expenses and other current assets | |
| 1,431 | | |
| 1,265 | |
Total current assets | |
| 18,686 | | |
| 21,362 | |
| |
| | | |
| | |
Operating lease right-of-use asset | |
| 220 | | |
| 229 | |
| |
| | | |
| | |
Total assets | |
$ | 18,906 | | |
$ | 21,591 | |
| |
| | | |
| | |
LIABILITIES AND EQUITY | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable | |
$ | 600 | | |
$ | 525 | |
Accrued expenses | |
| 1,363 | | |
| 1,946 | |
Operating lease liability | |
| 36 | | |
| 29 | |
Total current liabilities | |
| 1,999 | | |
| 2,500 | |
| |
| | | |
| | |
Operating lease liability, non-current | |
| 194 | | |
| 203 | |
Total liabilities | |
| 2,193 | | |
| 2,703 | |
| |
| | | |
| | |
Commitments and contingencies (Note 10) | |
| - | | |
| - | |
| |
| | | |
| | |
Equity: | |
| | | |
| | |
Shareholders’ equity: | |
| | | |
| | |
Preferred stock, par value $100 per share; 19,860 shares authorized; no shares issued or outstanding | |
| - | | |
| - | |
Series A convertible preferred stock, par value $100 per share; 140 shares authorized; no shares issued or outstanding | |
| - | | |
| - | |
Preferred stock, value | |
| - | | |
| - | |
Common stock, par value $.01 per share; 100,000,000 shares authorized; 32,196,862 shares issued and outstanding as of January 31, 2025 and October 31, 2024 | |
| 322 | | |
| 322 | |
Additional paid-in capital | |
| 261,470 | | |
| 260,432 | |
Accumulated deficit | |
| (243,934 | ) | |
| (240,750 | ) |
Treasury stock, 2,000 shares at cost | |
| (6 | ) | |
| (6 | ) |
Total shareholders’ equity | |
| 17,852 | | |
| 19,998 | |
Noncontrolling interest (Note 2) | |
| (1,139 | ) | |
| (1,110 | ) |
Total equity | |
| 16,713 | | |
| 18,888 | |
| |
| | | |
| | |
Total liabilities and equity | |
$ | 18,906 | | |
$ | 21,591 | |
The accompanying notes are an integral part of these
condensed consolidated financial statements.
ANIXA BIOSCIENCES, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(UNAUDITED)
(in thousands, except per share data)
| |
2025 | | |
2024 | |
| |
For the Three Months Ended January 31, | |
| |
2025 | | |
2024 | |
| |
| | |
| |
Revenue | |
$ | - | | |
$ | - | |
| |
| | | |
| | |
Operating costs and expenses: | |
| | | |
| | |
Research and development expenses (including non-cash stock-based compensation expenses of $397 and $489, respectively) | |
| 1,552 | | |
| 1,349 | |
General and administrative expenses (including non-cash stock-based compensation expenses of $658 and $771, respectively) | |
| 1,834 | | |
| 2,260 | |
Total operating costs and expenses | |
| 3,386 | | |
| 3,609 | |
| |
| | | |
| | |
Loss from operations | |
| (3,386 | ) | |
| (3,609 | ) |
| |
| | | |
| | |
Interest income | |
| 173 | | |
| 319 | |
| |
| | | |
| | |
Net loss | |
| (3,213 | ) | |
| (3,290 | ) |
| |
| | | |
| | |
Less: Net loss attributable to noncontrolling interest | |
| (29 | ) | |
| (35 | ) |
| |
| | | |
| | |
Net loss attributable to common shareholders | |
$ | (3,184 | ) | |
$ | (3,255 | ) |
| |
| | | |
| | |
Net loss per common share attributable to common shareholders: | |
| | | |
| | |
Basic and diluted | |
$ | (0.10 | ) | |
$ | (0.10 | ) |
| |
| | | |
| | |
Weighted average common shares outstanding: | |
| | | |
| | |
Basic and diluted | |
| 32,197 | | |
| 31,446 | |
The accompanying notes are an integral part of these
condensed consolidated financial statements.
ANIXA BIOSCIENCES, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF EQUITY
(in thousands, except share data)
FOR THE THREE MONTHS ENDED JANUARY 31, 2025 (UNAUDITED)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common Stock |
|
|
Additional
Paid-in
Capital |
|
|
Accumulated
Deficit |
|
|
Treasury
Stock |
|
|
Total
Shareholders’
Equity |
|
|
Non-
controlling
Interest |
|
|
Total
Equity |
|
|
|
Shares |
|
|
Par Value |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance, October 31, 2024 |
|
|
32,196,862 |
|
|
$ |
322 |
|
|
$ |
260,432 |
|
|
$ |
(240,750 |
) |
|
$ |
(6 |
) |
|
$ |
19,998 |
|
|
$ |
(1,110 |
) |
|
$ |
18,888 |
|
Stock option compensation to employees and directors |
|
|
- |
|
|
|
- |
|
|
|
1,031 |
|
|
|
- |
|
|
|
- |
|
|
|
1,031 |
|
|
|
- |
|
|
|
1,031 |
|
Stock options issued to consultants |
|
|
- |
|
|
|
- |
|
|
|
24 |
|
|
|
- |
|
|
|
- |
|
|
|
24 |
|
|
|
- |
|
|
|
24 |
|
Common stock issued to consultants |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common stock issued to consultants, shares |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common stock issued in an at-the-market offering, net of offering expenses |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common stock issued in an at-the-market offering, net of offering expenses, shares |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common stock issued upon exercise of stock options |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common stock issued upon exercise of stock options, shares |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Expenses related to an at-the-market offering |
|
|
- |
|
|
|
- |
|
|
|
(17 |
) |
|
|
- |
|
|
|
- |
|
|
|
(17 |
) |
|
|
- |
|
|
|
(17 |
) |
Net loss |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
(3,184 |
) |
|
|
- |
|
|
|
(3,184 |
) |
|
|
(29 |
) |
|
|
(3,213 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance, January 31, 2025 |
|
|
32,196,862 |
|
|
$ |
322 |
|
|
$ |
261,470 |
|
|
$ |
(243,934 |
) |
|
$ |
(6 |
) |
|
$ |
17,852 |
|
|
$ |
(1,139 |
) |
|
$ |
16,713 |
|
FOR THE THREE MONTHS ENDED JANUARY 31, 2024
(UNAUDITED)
|
|
Shares |
|
|
Par
Value |
|
|
Paid-in
Capital |
|
|
Accumulated
Deficit |
|
|
Shareholders’
Equity |
|
|
controlling
Interest |
|
|
Total
Equity |
|
|
|
Common Stock |
|
|
Additional |
|
|
|
|
|
Total |
|
|
Non- |
|
|
|
|
|
|
Shares |
|
|
Par
Value |
|
|
Paid-in
Capital |
|
|
Accumulated
Deficit |
|
|
Shareholders’
Equity |
|
|
controlling
Interest |
|
|
Total
Equity |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance, October 31, 2023 |
|
|
31,145,219 |
|
|
$ |
311 |
|
|
$ |
252,222 |
|
|
$ |
(228,196 |
) |
|
$ |
24,337 |
|
|
$ |
(966 |
) |
|
$ |
23,371 |
|
Balance |
|
|
31,145,219 |
|
|
$ |
311 |
|
|
$ |
252,222 |
|
|
$ |
(228,196 |
) |
|
$ |
24,337 |
|
|
$ |
(966 |
) |
|
$ |
23,371 |
|
Stock option compensation to employees and directors |
|
|
- |
|
|
|
- |
|
|
|
1,108 |
|
|
|
- |
|
|
|
1,108 |
|
|
|
- |
|
|
|
1,108 |
|
Stock options issued to consultants |
|
|
- |
|
|
|
- |
|
|
|
56 |
|
|
|
- |
|
|
|
56 |
|
|
|
- |
|
|
|
56 |
|
Common stock issued to consultants |
|
|
29,336 |
|
|
|
1 |
|
|
|
95 |
|
|
|
- |
|
|
|
96 |
|
|
|
- |
|
|
|
96 |
|
Common stock issued in an at-the-market offering, net of offering expenses of $68 |
|
|
555,820 |
|
|
|
6 |
|
|
|
2,190 |
|
|
|
- |
|
|
|
2,196 |
|
|
|
- |
|
|
|
2,196 |
|
Common stock issued upon exercise of stock options |
|
|
24,000 |
|
|
|
- |
|
|
|
67 |
|
|
|
- |
|
|
|
67 |
|
|
|
- |
|
|
|
67 |
|
Net loss |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
(3,255 |
) |
|
|
(3,255 |
) |
|
|
(35 |
) |
|
|
(3,290 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance, January 31, 2024 |
|
|
31,754,375 |
|
|
$ |
318 |
|
|
$ |
255,738 |
|
|
$ |
(231,451 |
) |
|
$ |
24,605 |
|
|
$ |
(1,001 |
) |
|
$ |
23,604 |
|
Balance |
|
|
31,754,375 |
|
|
$ |
318 |
|
|
$ |
255,738 |
|
|
$ |
(231,451 |
) |
|
$ |
24,605 |
|
|
$ |
(1,001 |
) |
|
$ |
23,604 |
|
The accompanying notes are an integral part of these
condensed consolidated financial statements.
ANIXA BIOSCIENCES, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(UNAUDITED)
(in thousands)
| |
2025 | | |
2024 | |
| |
For the three months ended January 31, | |
| |
2025 | | |
2024 | |
Cash flows from operating activities: | |
| | | |
| | |
Reconciliation of net loss to net cash used in operating activities: | |
| | | |
| | |
Net loss | |
$ | (3,213 | ) | |
$ | (3,290 | ) |
Stock option compensation to employees and directors | |
| 1,031 | | |
| 1,108 | |
Stock options issued to consultants | |
| 24 | | |
| 56 | |
Common stock issued to consultants | |
| - | | |
| 96 | |
Amortization of operating lease right-of-use asset | |
| 9 | | |
| 13 | |
Amortization of discount on held-to-maturity securities | |
| (252 | ) | |
| - | |
Change in operating assets and liabilities: | |
| | | |
| | |
Receivables | |
| 173 | | |
| (121 | ) |
Prepaid expenses and other current assets | |
| (166 | ) | |
| 212 | |
Accounts payable | |
| 75 | | |
| 158 | |
Accrued expenses | |
| (583 | ) | |
| (528 | ) |
Operating lease liability | |
| (2 | ) | |
| (13 | ) |
Net cash used in operating activities | |
| (2,904 | ) | |
| (2,309 | ) |
| |
| | | |
| | |
Cash flows from investing activities: | |
| | | |
| | |
Disbursements to acquire short-term investments | |
| (12,997 | ) | |
| (20,020 | ) |
Proceeds from maturities of short-term investments | |
| 15,700 | | |
| 20,149 | |
Net cash provided by investing activities | |
| 2,703 | | |
| 129 | |
| |
| | | |
| | |
Cash flows from financing activities: | |
| | | |
| | |
Net (expenses) proceeds from an at-the-market
offering | |
| (17 | ) | |
| 2,196 | |
Proceeds from exercise of stock options | |
| - | | |
| 67 | |
Net cash (used in) provided by financing activities | |
| (17 | ) | |
| 2,263 | |
| |
| | | |
| | |
Net (decrease) increase in cash and cash equivalents | |
| (218 | ) | |
| 83 | |
Cash and cash equivalents at beginning of period | |
| 1,271 | | |
| 915 | |
Cash and cash equivalents at end of period | |
$ | 1,053 | | |
$ | 998 | |
The accompanying notes are an integral part of these
condensed consolidated financial statements.
ANIXA BIOSCIENCES, INC. AND SUBSIDIARIES
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
(UNAUDITED)
1. BUSINESS AND FUNDING
Description of Business
As used herein, “we,”
“us,” “our,” the “Company” or “Anixa” means Anixa Biosciences, Inc. and its consolidated
subsidiaries.
Anixa Biosciences, Inc. is a biotechnology
company developing therapies and vaccines that are focused on critical unmet needs in oncology. Our therapeutics program consists of the
development of a chimeric endocrine receptor-T cell therapy, a novel form of chimeric antigen receptor-T cell (“CAR-T”) technology,
initially focused on treating ovarian cancer, which is being developed at our subsidiary, Certainty Therapeutics, Inc. (“Certainty”).
Our vaccine programs include (i) the development of a vaccine against breast cancer, initially focused on triple negative breast cancer
(“TNBC”), the most lethal form of breast cancer, (ii) the development of a vaccine against ovarian cancer, and (iii) a vaccine
discovery program utilizing the same mechanism as our breast and ovarian cancer vaccines, to develop additional cancer vaccines to address
many intractable cancers, including high incidence malignancies in lung, colon and prostate.
Our subsidiary, Certainty, is
developing immuno-therapy drugs against cancer. Certainty holds an exclusive worldwide, royalty-bearing license to use certain intellectual
property owned or controlled by The Wistar Institute (“Wistar”), the nation’s first independent biomedical research
institute and a leading NCI designated cancer research center, relating to Wistar’s chimeric endocrine receptor targeted therapy
technology. We have initially focused on the development of a treatment for ovarian cancer, but we also may pursue applications of the
technology for the development of treatments for additional solid tumors. The license agreement requires Certainty to make certain cash
and equity payments to Wistar upon achievement of specific development milestones. With respect to Certainty’s equity obligations
to Wistar, Certainty issued to Wistar shares of its common stock equal to five percent (5%) of the common stock of Certainty, such equity
stake subject to dilution by further funding of Certainty’s activities by the Company. Due to such Company funding, Wistar’s
equity stake in Certainty was 4.3% as of January 31, 2025.
Certainty, in collaboration with
the H. Lee Moffitt Cancer Center and Research Institute, Inc. (“Moffitt”), has begun human clinical testing of the CAR-T technology
licensed by Certainty from Wistar aimed initially at treating ovarian cancer. After receiving authorization from the FDA, we commenced
enrollment of patients in a Phase 1 clinical trial and treated the first patient in August 2022. Further, in May 2023 and August 2023,
we treated the second and third patients in the trial, respectively, at the same dose level as the first patient, and the treatment was
well-tolerated by the patients. In February 2024, May 2024 and June 2024, we treated the three patients, respectively, of the second dose
cohort, where the patients were administered a three-times higher dose of cells than the patients in the first cohort. The treatment at
this dose level has also been well-tolerated by the patients. While the dose levels in the first two cohorts were expected to be sub-therapeutic,
two of the six patients exhibited some anecdotal signs of efficacy. Both have shown possible signs of tumor necrosis, and one is still
alive nearly 2 years past initial treatment. In the case of this patient, due to the encouraging results with her initial treatment, we
sought single patient Investigational New Drug (“IND”) application permission from the FDA to re-dose her. This re-dosing
was approved by the FDA, and we administered her second treatment in October 2024. This second treatment appears to have been well-tolerated
by the patient. From November 2024 to February 2025, we treated three patients in the third dose cohort, where they were administered
a ten-times higher dose of cells than the patients in the first dose cohort. Consistent with the lower dose cohorts, the treatment appears
to have been well-tolerated by the patients. As of March 11, 2025, we are preparing to enroll patients in the 4th dose cohort,
where we will be administering a 30-times higher dose than the original dose cohort.
This study is a dose-escalation
trial with two arms based on route of delivery—intraperitoneal or intravenous—to determine the maximum tolerated dose in patients
with recurrent epithelial ovarian cancer and to assess persistence, expansion and efficacy of the modified T cells. The study is being
conducted at Moffitt and will consist of up to 24 to 48 patients who have received at least two prior lines of chemotherapy. The study
is estimated to be completed in two to three years depending on multiple factors including when the maximum tolerated dose is reached,
the rate of patient enrollment, the significance of efficacy data and how long we maintain the two different delivery methods.
We hold an exclusive worldwide,
royalty-bearing license to use certain intellectual property owned or controlled by The Cleveland Clinic Foundation (“Cleveland
Clinic”) relating to certain breast cancer vaccine technology developed at Cleveland Clinic. The license agreement requires us to
make certain cash payments to Cleveland Clinic upon achievement of specific development milestones. Utilizing this technology, we are
working in collaboration with Cleveland Clinic to develop a method to vaccinate women against breast cancer, focused initially on TNBC.
The focus of this vaccine is a specific protein, α-lactalbumin, that is only expressed during lactation in a healthy woman’s
mammary tissue. This protein disappears when the woman is no longer lactating, but reappears in many forms of breast cancer, especially
TNBC. Studies have shown that vaccinating against this protein prevents breast cancer in mice.
In October 2021, following the
U.S. Food and Drug Administration’s (“FDA”) authorization to proceed, we commenced dosing patients in a Phase 1 clinical
trial of our breast cancer vaccine. This study, which is being fully funded by a U.S. Department of Defense grant to Cleveland Clinic,
is a multiple-ascending dose Phase 1 trial to determine the maximum tolerated dose (“MTD”) of the vaccine in patients with
early-stage, triple-negative breast cancer as well as monitor immune response. The study is being conducted at Cleveland Clinic. During
the course of the Phase 1 study, participants will receive three vaccinations, each two weeks apart, and will be closely monitored for
side effects and immune response. The first segment of the study, Phase 1a, will consist of approximately 24 patients who have completed
treatment for early-stage, triple-negative breast cancer within the past three years and are currently tumor-free but at high risk for
recurrence. Studies show that 42% of TNBC patients will have a recurrence of their cancer, with most of the recurrences occurring in the
first two to three years after standard of care treatment. In January 2023, the number of participants in each dose cohort was expanded,
and as of August 2023, we had completed vaccinating all patients in these expanded cohorts. In December 2023, we presented the immunological
data collected to date at the San Antonio Breast Cancer Symposium. The data presented show that in the vaccinated women who had been tested
to date, various levels of antigen-specific T cell responses were observed at all dose levels. Subsequently, we began vaccinating participants
in additional dose cohorts at varying dose levels of the different key components of the vaccine. Further, in November 2023, we commenced
vaccination of participants in the second segment of the trial, Phase 1b, that includes participants who have never had cancer, but carry
certain mutations in genes such as BRCA1, BRCA2 or PALB2, that indicate a greater risk of developing TNBC in the future, and have elected
to have a prophylactic mastectomy. Finally, in January 2024, we commenced vaccination of participants in the third segment of the trial,
Phase 1c, that includes post-operative TNBC patients that have residual disease following treatment and are currently undergoing treatment
with pembrolizumab (Keytruda®). In November 2024, we presented the most recent data from each of the three arms of the trial at the
Society for Immunotherapy of Cancer (SITC) Annual Meeting. Key findings presented include i) patients exhibited antigen-specific immune
responses at all dose levels and in all three patient groups (Phase 1a, 1b and 1c), ii) patients receiving our vaccine in combination
with Keytruda are not showing any additional or more severe adverse side effects, and iii) no adverse side effects were seen other than
varying degrees of injection site irritation. These findings are promising, and as we continue the Phase 1 trial, we are preparing to
initiate a Phase 2 clinical trial in the neo-adjuvant setting (pre-surgery) to determine possible therapeutic effect of the vaccine. We
anticipate commencing the Phase 2 trial in 2025.
We hold an exclusive worldwide,
royalty-bearing license to use certain intellectual property owned or controlled by Cleveland Clinic relating to certain ovarian cancer
vaccine technology. The license agreement requires us to make certain cash payments to Cleveland Clinic upon achievement of specific development
milestones. This technology pertains to among other things, the use of vaccines for the treatment or prevention of ovarian cancers which
express the anti-Mullerian hormone receptor 2 protein containing an extracellular domain (“AMHR2-ED”). In healthy tissue,
this protein regulates growth and development of egg-containing follicles in the ovary. While expression of AMHR2-ED naturally and markedly
declines during menopause, this protein is expressed at high levels in the ovaries of postmenopausal women with ovarian cancer. Researchers
at Cleveland Clinic believe that a vaccine targeting AMHR2-ED could prevent the occurrence of ovarian cancer.
In May 2021, Cleveland Clinic
was granted acceptance for our ovarian cancer vaccine technology into the National Cancer Institute’s (“NCI”) PREVENT
program. The NCI is a part of the National Institutes of Health (“NIH”). The PREVENT program is a peer-reviewed agent development
program designed to support pre-clinical development of innovative interventions and biomarkers for cancer prevention and interception
towards clinical trials. The scientific and financial resources of the PREVENT program are being used for our ovarian cancer vaccine technology
to perform virtually all pre-clinical research and development, manufacturing and IND enabling studies. This work is being performed at
NCI facilities, by NCI scientific staff and with NCI financial resources and will require no material financial expenditures by the Company,
nor the payment of any future consideration by the Company to NCI.
In May 2024, based on the positive
clinical results to date in the development of our breast cancer vaccine, we entered into a Joint Development and Option Agreement with
Cleveland Clinic to collaborate in efforts to develop additional vaccines for the prevention or treatment of cancers. Working with Cleveland
Clinic researchers, we are focusing on the same novel scientific mechanism as in our breast and ovarian cancer vaccines, and working to
discover additional retired proteins that may be associated with other forms of cancer, specifically high incidence malignancies in the
lung, colon and prostate.
Over the next several quarters,
we expect the development of our therapeutics and vaccines to be the primary focus of the Company. As part of our legacy operations, the
Company remains engaged in limited patent licensing activities of its various patent portfolios. We do not expect these activities to
be a significant part of the Company’s ongoing operations nor do we expect these activities to require material financial resources
or attention of senior management.
Over the past several years, our
revenue was derived from technology licensing and the sale of patented technologies, including revenue from the settlement of litigation.
We have not generated any revenue to date from our vaccine or therapeutics programs. In addition, while we pursue our vaccine and therapeutics
programs, we may also make investments in and form new companies to develop additional emerging technologies. We do not expect to begin
generating revenue with respect to any of our current vaccine or therapy programs in the near term. We hope to achieve a profitable outcome
by eventually licensing our technologies to large pharmaceutical companies that have the resources and infrastructure in place to manufacture,
market and sell our technologies as vaccines or therapeutics. The eventual licensing of any of our technologies may take several years,
if it is to occur at all, and may depend on positive results from human clinical trials.
Funding and Management’s Plans
Based on currently available information as of March 11, 2025, we believe
that our existing cash, cash equivalents and short-term investments will be sufficient to fund our activities for at least the next twelve
months. The Company had approximately $18,686,000 of total current assets at January 31, 2025 compared to approximately $21,362,000 at
October 31, 2024 which is a reduction of approximately $2,676,000 for the three months ended January 31, 2025. Therefore, the Company
believes that it has sufficient cash, cash equivalents and short-term investments to operate its business, as currently contemplated,
for significantly longer than 12 months from the date of this Report. We have implemented a business model that conserves funds by collaborating
with third parties to develop our technologies. During the three months ended January 31, 2025, we did not issue any shares under our
at-the-market equity offering. Under our at-the-market equity program, which is currently effective and may remain available for us to
use in the future, as of January 31, 2025, we may sell approximately $97 million of common stock.
2. SIGNIFICANT ACCOUNTING POLICIES
Basis of Presentation
The accompanying unaudited condensed
consolidated financial statements have been prepared in accordance with generally accepted accounting principles in the United States
of America (“US GAAP”) for interim financial information and with the instructions to Form 10-Q and Rule 8-03 of Regulation
S-X. Accordingly, certain information and disclosures required by generally accepted accounting principles in annual financial statements
have been omitted or condensed. These interim condensed consolidated financial statements should be read in conjunction with the audited
consolidated financial statements and related disclosures included in our Annual Report on Form 10-K for the fiscal year ended October
31, 2024. The accompanying October 31, 2024 condensed consolidated balance sheet data was derived from the audited financial statements
but does not include all disclosures required by US GAAP. The condensed consolidated financial statements include all adjustments of a
normal recurring nature which, in the opinion of management, are necessary for a fair statement of our financial position as of January
31, 2025, and results of operations and cash flows for the interim periods represented. The results of operations for the three months
ended January 31, 2025 are not necessarily indicative of the results to be expected for the year.
Noncontrolling Interest
Noncontrolling interest represents
Wistar’s equity ownership in Certainty and is presented as a component of equity. The following table sets forth the changes in
noncontrolling interest for the three months ended January 31, 2025 (in thousands):
SCHEDULE OF CHANGES IN NONCONTROLLING INTEREST
Balance, October 31, 2024 | |
$ | (1,110 | ) |
Net loss attributable to noncontrolling interest | |
| (29 | ) |
Balance, January 31, 2025 | |
$ | (1,139 | ) |
Revenue Recognition
Our revenue
has been derived solely from technology licensing and the sale of patented technologies. Revenue is recognized upon transfer of control
of intellectual property rights and satisfaction of other contractual performance obligations to licensees in an amount that reflects
the consideration we expect to receive.
Our revenue
recognition policy requires us to make certain judgments and estimates in connection with the accounting for revenue. Such areas may include
determining the existence of a contract and identifying each party’s rights and obligations to transfer goods and services, identifying
the performance obligations in the contract, determining the transaction price and allocating the transaction price to separate performance
obligations, estimating the timing of satisfaction of performance obligations, determining whether a promise to grant a license is distinct
from other promised goods or services and evaluating whether a license transfers to a customer at a point in time or over time.
Our revenue
arrangements provide for the payment, within 30 days of execution of the agreement, of contractually determined, one-time, paid-up license
fees in settlement of litigation and in consideration for the grant of certain intellectual property rights for patented technologies
owned or controlled by the Company. These arrangements typically include some combination of the following: (i) the grant of a non-exclusive,
retroactive and future license to manufacture and/or sell products covered by patented technologies owned or controlled by the Company,
(ii) a covenant-not-to-sue, (iii) the release of the licensee from certain claims, and (iv) the dismissal of any pending litigation. In
such instances, the intellectual property rights granted have been perpetual in nature, extending until the expiration of the related
patents. Pursuant to the terms of these agreements, we have no further obligations with respect to the granted intellectual property rights,
including no obligation to maintain or upgrade the technology, or provide future support or services. Licensees obtained control of the
intellectual property rights they have acquired upon execution of the agreement. Accordingly, the performance obligations from these agreements
were satisfied and 100% of the revenue was recognized upon the execution of the agreements.
Cost of Revenues
Cost of revenues include the costs
and expenses incurred in connection with our patent licensing and enforcement activities, including inventor royalties paid to original
patent owners, contingent legal fees paid to external counsel, other patent-related legal expenses paid to external counsel, licensing
and enforcement related research and consulting and other expenses paid to third-parties. These costs are included under the caption “Operating
costs and expenses” in the accompanying consolidated statements of operations.
Research and Development Expenses
Research and development expenses
consist primarily of employee compensation, payments to third parties for research and development activities and other direct costs associated
with developing our therapeutics and vaccines. We recognize research and development expenses as incurred. Advance payments for future
research and development activities are deferred and expensed as the services are performed. We recognize our preclinical studies and
clinical trial expenses based on the services performed pursuant to contracts with research institutions, clinical research organizations
(“CROs”), clinical manufacturing organizations (“CMOs”), and other parties that conduct and manage various stages
of research and development activities on our behalf. Fees for such services are recognized based on management’s estimates after
considering the activities and tasks completed by each service provider in a given period, the time period over which services are expected
to be performed, and the level of effort expended in each reporting period.
At each
balance sheet date, management estimates prepaid and accrued research and development costs by discussing progress or stage of completion
of activities with internal personnel and external service providers, and comparing this information to payments made, invoices received,
and the agreed-upon contractual fee to be paid for such services in the applicable contract or statements of work.
In addition,
we allocate certain internal compensation costs to research and development expenses based on management’s estimates of each employee’s
time and effort expended.
Investment Policy
The Company’s investment
policy is designed to optimize returns while managing risk and liquidity. The policy allows for investments in a diversified range of
financial instruments, including U.S. government debt securities with fixed maturities and contractual cash flows, as well as alternative
investments such as Bitcoin and Bitcoin-based exchange traded funds (collectively, the “Bitcoin Assets”).
The Company acquires U.S. government
debt securities that it has the positive intent and ability to hold to maturity. These securities are recorded at amortized cost, net
of any applicable discount which is amortized to interest income, and are accounted for as held-to-maturity securities. The Company’s
Bitcoin Assets are measured at fair value based on quoted prices on active exchanges. The Company recognizes changes in the fair value
of Bitcoin Assets as gains or losses in the statement of operations during the period in which they occur.
3. STOCK-BASED COMPENSATION
The Company maintains stock equity
incentive plans under which the Company may grant incentive stock options, non-qualified stock options, stock appreciation rights, stock
awards, performance awards, or stock units to employees, directors and consultants.
Stock Option Compensation Expense
We account for stock options granted
to employees, directors and consultants using the accounting guidance in ASC 718, Stock Compensation. We estimate the fair value of service-based
stock options on the date of grant, using the Black-Scholes pricing model, and recognize compensation expense over the requisite service
period of the grant. We recorded stock-based compensation expense related to service-based stock options granted to employees and directors
of approximately $1,031,000 and $1,108,000 during the three months ended January 31, 2025 and 2024.
The compensation cost for service-based
stock options granted to consultants is measured at the grant date, based on the fair value of the award using the Black-Scholes pricing
model, and is expensed on a straight-line basis over the requisite service period (the vesting period of the stock option) which is one
to three years. We recorded stock-based consulting expense related to stock options granted to consultants of approximately $24,000 and
$56,000 during the three months ended January 31, 2025 and 2024, respectively.
Stock Option Activity
During the three months ended
January 31, 2025 and 2024, we granted options to purchase 1,355,000 shares and 1,335,000 shares of common stock, respectively, to employees
and consultants, with exercise prices ranging from $2.37 to $4.39 per share, pursuant to the 2018 Share Plan. During the three months
ended January 31, 2025, no stock options were exercised. During the three months ended January 31, 2024, stock options to purchase 24,000
shares of common stock were exercised on a cash basis, with aggregate proceeds of approximately $67,000.
Stock Option Plans
During the three months ended
January 31, 2025, we had two stock option plans: the Anixa Biosciences, Inc. 2010 Share Incentive Plan (the “2010 Share Plan”)
and the Anixa Biosciences, Inc. 2018 Share Incentive Plan (the “2018 Share Plan”), which were adopted by our Board of Directors
on July 14, 2010 and January 25, 2018, respectively. The 2018 Share Plan was approved by our shareholders on March 29, 2018.
2010 Share Plan
The 2010 Share Plan provided for
the grant of nonqualified stock options, stock appreciation rights, stock awards, performance awards and stock units to employees, directors
and consultants. In accordance with the provisions of the 2010 Share Plan, the plan terminated with respect to the ability to grant future
awards on July 14, 2020. Information regarding the 2010 Share Plan for the three months ended January 31, 2025 is as follows:
SCHEDULE OF OPTION ACTIVITY
| |
Shares | | |
Weighted Average Exercise Price Per Share | | |
Aggregate Intrinsic Value (in thousands) | |
Options outstanding at October 31, 2024 | |
| 986,968 | | |
$ | 2.77 | | |
| | |
Options outstanding and exercisable at January 31, 2025 | |
| 986,968 | | |
$ | 2.77 | | |
$ | 566 | |
The following table summarizes
information about stock options outstanding and exercisable under the 2010 Share Plan as of January 31, 2025:
SCHEDULE
OF OPTIONS OUTSTANDING AND EXERCISABLE
Range of
Exercise Prices |
|
|
Number
Outstanding and
Exercisable |
|
|
Weighted Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
0.67 - $2.27 |
|
|
|
316,000 |
|
|
|
2.5 |
|
|
$ |
1.11 |
|
$ |
2.58 - $3.13 |
|
|
|
251,968 |
|
|
|
1.1 |
|
|
$ |
2.93 |
|
$ |
3.46 - $5.30 |
|
|
|
419,000 |
|
|
|
3.2 |
|
|
$ |
3.93 |
|
2018 Share Plan
The 2018 Share Plan provides for
the grant of incentive stock options, nonqualified stock options, stock appreciation rights, stock awards, performance awards and stock
units to employees, directors and consultants. As of January 31, 2025, the 2018 Share Plan had 645,000 shares available for future grants.
Information regarding the 2018 Share Plan for the three months ended January 31, 2025 is as follows:
SCHEDULE
OF OPTION ACTIVITY
|
|
Shares |
|
|
Weighted
Average Exercise
Price Per Share |
|
|
Aggregate
Intrinsic Value
(in thousands) |
|
Options outstanding at October 31, 2024 |
|
|
11,171,094 |
|
|
$ |
3.74 |
|
|
|
|
|
Granted |
|
|
1,355,000 |
|
|
|
2.37 |
|
|
|
|
|
Forfeited/expired |
|
|
(25,000 |
) |
|
|
3.96 |
|
|
|
|
|
Options outstanding at January 31, 2025 |
|
|
12,501,094 |
|
|
$ |
3.59 |
|
|
$ |
1,093 |
|
Options exercisable at January 31, 2025 |
|
|
8,260,549 |
|
|
$ |
3.56 |
|
|
$ |
391 |
|
The following table summarizes
information about stock options outstanding and exercisable under the 2018 Share Plan as of January 31, 2025:
SCHEDULE
OF OPTIONS OUTSTANDING AND EXERCISABLE
|
|
|
Options Outstanding |
|
|
Options Exercisable |
|
Range of
Exercise Prices |
|
|
Number
Outstanding |
|
|
Weighted
Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
|
Number
Exercisable |
|
|
Weighted
Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
2.09 - $3.87 |
|
|
|
6,663,879 |
|
|
|
6.5 |
|
|
$ |
3.06 |
|
|
|
5,168,886 |
|
|
|
5.5 |
|
|
$ |
3.22 |
|
$ |
4.02 - $5.30 |
|
|
|
5,837,215 |
|
|
|
7.4 |
|
|
$ |
4.20 |
|
|
|
3,091,663 |
|
|
|
7.2 |
|
|
$ |
4.13 |
|
Employee Stock Purchase Plan
The Company maintains the Anixa
Biosciences, Inc. Employee Stock Purchase Plan (the “ESPP”) which permits eligible employees to purchase shares at not less
than 85% of the market value of the Company’s common stock on the offering date or the purchase date of the applicable offering
period, whichever is lower. The ESPP was adopted by our Board of Directors on August 13, 2018 and approved by our shareholders on September
27, 2018. During the three months ended January 31, 2025 and 2024, no shares were purchased under the ESPP.
Warrants
As of January 31, 2025, we had
warrants outstanding to purchase 300,000 shares of common stock at $6.56 per share, issued during fiscal year 2021 and expiring on March
22, 2026.
Information regarding the Company’s
warrants for the three months ended January 31, 2025 is as follows:
SCHEDULE
OF WARRANTS ACTIVITY
|
|
Shares |
|
|
Weighted
Average Exercise
Price Per Share |
|
|
Aggregate
Intrinsic
Value |
|
Warrants outstanding at October 31, 2024 |
|
|
300,000 |
|
|
$ |
6.56 |
|
|
|
|
|
Warrants outstanding and exercisable at January 31, 2025 |
|
|
300,000 |
|
|
$ |
6.56 |
|
|
$ |
0 |
|
The following table summarizes
information about the Company’s outstanding and exercisable warrants as of January 31, 2025:
SCHEDULE OF OUTSTANDING AND EXERCISABLE
Range of
Exercise Prices |
|
|
Number
Outstanding and
Exercisable |
|
|
Weighted Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
6.56 |
|
|
|
300,000 |
|
|
|
1.1 |
|
|
$ |
6.56 |
|
Stock Awards
During the three months ended
January 31, 2025, we did not issue any stock awards. During the three months ended January 31, 2024, we issued 29,336 shares of common
stock to consultants providing investor relations services, and recorded expense of approximately $96,000.
Treasury stock
As of January 31, 2025, the Company
held 2,000 shares of its common stock as treasury stock. These shares were repurchased during the fiscal year ended October 31, 2024,
at an average cost of $3.17 per share for a total cost of approximately $6,000. The repurchases were made as part of a stock buyback program
approved by our Board of Directors on July 11, 2024. The treasury shares are accounted for under the cost method and are recorded as a
reduction in shareholders’ equity in the consolidated balance sheet. The Company may reissue treasury shares for stock option exercises,
acquisitions, or other corporate purposes.
4. FAIR VALUE MEASUREMENTS
US GAAP defines fair value and
establishes a framework for measuring fair value. We have categorized our financial assets and liabilities, based on the priority of the
inputs to the valuation technique, into a three-level fair value hierarchy as set forth below. If the inputs used to measure the financial
instruments fall within different levels of the hierarchy, the categorization is based on the lowest level input that is significant to
the fair value measurement of the instrument.
Financial assets and liabilities
recorded in the accompanying condensed consolidated balance sheets are categorized based on the inputs to the valuation techniques as
follows:
Level 1 – Financial instruments
whose values are based on unadjusted quoted prices for identical assets or liabilities in an active market which we have the ability to
access at the measurement date.
Level 2 – Financial instruments
whose values are based on quoted market prices in markets where trading occurs infrequently or whose values are based on quoted prices
of instruments with similar attributes in active markets.
Level 3 – Financial instruments
whose values are based on prices or valuation techniques that require inputs that are both unobservable and significant to the overall
fair value measurement. These inputs reflect management’s own assumptions about the assumptions a market participant would use in
pricing the instrument.
The following table presents the
hierarchy for our financial assets measured at fair value on a recurring basis as of January 31, 2025 (in thousands):
SCHEDULE OF FINANCIAL ASSETS MEASURED AT FAIR VALUE ON A RECURRING BASIS
| |
Level 1 | | |
Level 2 | | |
Level 3 | | |
Total | |
Money market funds: | |
| | | |
| | | |
| | | |
| | |
Cash equivalents | |
$ | 912 | | |
$ | - | | |
$ | - | | |
$ | 912 | |
Bitcoin exchange traded funds: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 10 | | |
| - | | |
| 10 | |
U.S. treasury bills: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 16,192 | | |
| - | | |
| 16,192 | |
Total financial assets | |
$ | 912 | | |
$ | 16,202 | | |
$ | - | | |
$ | 17,114 | |
The following table presents the
hierarchy for our financial assets measured at fair value on a recurring basis as of October 31, 2024 (in thousands):
| |
Level 1 | | |
Level 2 | | |
Level 3 | | |
Total | |
Money market funds: | |
| | | |
| | | |
| | | |
| | |
Cash equivalents | |
$ | 1,170 | | |
$ | - | | |
$ | - | | |
$ | 1,170 | |
U.S. treasury bills: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 18,653 | | |
| - | | |
| 18,653 | |
Total financial assets | |
$ | 1,170 | | |
$ | 18,653 | | |
$ | - | | |
$ | 19,823 | |
Our non-financial assets that
are measured at fair value on a non-recurring basis are property and equipment and other assets which are measured using fair value techniques
whenever events or changes in circumstances indicate a condition of impairment exists. The estimated fair value of prepaid expenses and
other current assets, accounts payable and accrued expenses approximates their individual carrying amounts due to the short-term nature
of these measurements. Cash equivalents are stated at carrying value which approximates fair value.
5. ACCRUED EXPENSES
Accrued expenses consist of the
following as of:
SCHEDULE OF ACCRUED EXPENSES
| |
January 31, | | |
October 31, | |
| |
2025 | | |
2024 | |
| |
(in thousands) | |
Payroll and related expenses | |
$ | 515 | | |
$ | 1,126 | |
Accrued royalty and contingent legal fees | |
| 626 | | |
| 626 | |
Accrued other | |
| 222 | | |
| 194 | |
Accrued expenses | |
$ | 1,363 | | |
$ | 1,946 | |
6. NET LOSS PER SHARE OF COMMON STOCK
Basic net loss per common share
(“Basic EPS”) is computed by dividing net loss by the weighted average number of common shares outstanding. Diluted net loss
per common share (“Diluted EPS”) is computed by dividing net loss by the weighted average number of common shares and dilutive
common share equivalents and convertible securities then outstanding. Diluted EPS for all periods presented is the same as Basic EPS,
as the inclusion of the effect of common share equivalents then outstanding would be anti-dilutive. For this reason, excluded from the
calculation of Diluted EPS for the three months ended January 31, 2025 and 2024, were stock options to purchase 13,488,062 and 12,497,094
shares, respectively, and warrants to purchase 300,000 and 300,000 shares, respectively.
7. EFFECT OF RECENTLY ADOPTED AND ISSUED PRONOUNCEMENTS
In November 2023, the FASB issued
Accounting Standards Update 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, to provide more disaggregated
expense information about a public entity’s reportable segments. The amendments in this update should be applied retrospectively
and are effective for fiscal years beginning after December 15, 2023, and interim periods beginning after December 15, 2024. We began
a detailed assessment of the impact that this guidance will have on our consolidated financial statements and related disclosures, and
our analysis is currently ongoing.
In December 2023, the FASB issued
Accounting Standards Update 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, to require disaggregated information
about a reporting entity’s effective tax rate reconciliation as well as information on income taxes paid. The amendments in this
update should be applied prospectively, with an option to apply them retrospectively, and are effective for fiscal years beginning after
December 15, 2024 for public entities. We began a detailed assessment of the impact that this guidance will have on our consolidated financial
statements and related disclosures, and our analysis is currently ongoing.
In March 2024, the FASB issued
Accounting Standards Update 2024-03, Income Statement—Reporting Comprehensive Income—Expense Disaggregation Disclosures (Subtopic
220-40): Disaggregation of Income Statement Expenses, to improve the disclosures about a public business entity’s expenses and to
provide more detailed information about the types of expenses in commonly presented expense captions. The amendments in this update should
be applied either prospectively or retrospectively, and are effective for fiscal years beginning after December 15, 2026, and interim
periods beginning after December 15, 2027. We began a detailed assessment of the impact that this guidance will have on our consolidated
financial statements and related disclosures, and our analysis is currently ongoing.
8. INCOME TAXES
We recognize deferred tax assets
and liabilities for the estimated future tax effects of events that have been recognized in our financial statements or tax returns. Under
this method, deferred tax assets and liabilities are determined based on the difference between the financial statement and tax bases
of assets and liabilities using enacted tax rates in effect in the years in which the differences are expected to reverse. A valuation
allowance is established, when necessary, to reduce deferred tax assets to the amount expected to be realized. We have provided a full
valuation allowance against our deferred tax asset due to our historical pre-tax losses and the uncertainty regarding the realizability
of these deferred tax assets.
We have substantial net operating
loss carryforwards for Federal and California income tax returns. These net operating loss carryforwards could be subject to limitations
under Internal Revenue Code section 382, the effects of which have not been determined by the Company. We have no unrecognized income
tax benefits as of January 31, 2025 and October 31, 2024 and we account for interest and penalties related to income tax matters, if any,
in general and administrative expenses.
9. LEASES
We lease approximately 2,000 square
feet of office space at 3150 Almaden Expressway, San Jose, California (our principal executive offices) from an unrelated party pursuant
to an operating lease that, as amended, will expire on September 30, 2027, with an option to extend the lease an additional two years.
The base rent is approximately $5,000 per month and the lease provides for annual increases of approximately 3% and an escalation clause
for increases in certain operating costs. The lease, as amended, resulted in a right-of-use asset and lease liability of approximately
$250,000 with a discount rate of 12%. Rent expense was approximately $16,000 and $17,000, respectively, for the three months ended January
31, 2025 and 2024.
For operating leases, the lease
liability is initially and subsequently measured at the present value of the unpaid lease payments. The remaining 56-month lease term
as of January 31, 2025 for the Company’s lease includes the noncancelable period of the lease and the additional two-year option
period that the Company is reasonably certain to exercise. All right-of-use assets are reviewed for impairment when indications of impairment
are present.
As of January 31, 2025, the annual
minimum future lease payments of our operating lease liability were as follows (in thousands):
SCHEDULE OF MINIMUM LEASE PAYMENTS
For Years Ended October 31, | |
Operating Leases | |
2025 (remaining) | |
$ | 47 | |
2026 | |
| 63 | |
2027 | |
| 64 | |
2028 | |
| 66 | |
2029 | |
| 63 | |
Total future minimum lease payments, undiscounted | |
| 303 | |
Less: Imputed interest | |
| 73 | |
Present value of future minimum lease payments | |
$ | 230 | |
| |
| | |
Balance as of January 31, 2025: | |
| | |
Operating lease liability | |
$ | 36 | |
Operating lease liability, non-current | |
| 194 | |
Total | |
$ | 230 | |
10. COMMITMENTS AND CONTINGENCES
Litigation Matters
Other than lawsuits related to
the enforcement of our patent rights, we are not a party to any material pending legal proceedings, nor are we aware of any pending litigation
or legal proceeding against us that would have a material adverse effect upon our results of operations or financial condition.
License Commitments
As of January 31, 2025, our commitments
under certain technology license agreements related to our therapeutic and vaccine development programs for the next twelve months, were
approximately $150,000.
Research & Development Agreements
We have entered into certain research
and development agreements with various collaboration partners and third-party vendors related to i) the manufacturing of materials necessary
for the expected Phase 2 clinical trial of our breast cancer vaccine, ii) the discovery of new vaccine targets in high incidence malignancies
in prostate, lung and colon and iii) the further development of our CAR-T technology. As of January 31, 2025, future payments the Company
may make under these agreements, dependent upon, among other things, development of analytical methods, formulation feasibility studies,
stability testing and results of manufacturing processes, may be approximately $3.7 million and such payments may be made over up to a
five-year period.
11. SEGMENT INFORMATION
We follow the accounting guidance
of ASC 280 “Segment Reporting” (“ASC 280”). Reportable operating segments are determined based on the management
approach. The management approach, as defined by ASC 280, is based on the way that the chief operating decision-maker organizes the segments
within an enterprise for making operating decisions and assessing performance. While our results of operations are primarily reviewed
on a consolidated basis, the chief operating decision-maker manages the enterprise in three reportable segments, each with different operating and potential revenue generating
characteristics: (i) Cancer Vaccines, (ii) CAR-T Therapeutics, and (iii) Other. The following represents selected financial information
for our segments for the three months ended January 31, 2025 and 2024 and as of January 31, 2025 and October 31, 2024 (in thousands):
SCHEDULE OF SEGMENT INFORMATION
| |
2025 | | |
2024 | |
| |
For the Three Months Ended January 31, | |
| |
2025 | | |
2024 | |
Net loss: | |
| | | |
| | |
Cancer Vaccines | |
$ | (2,018 | ) | |
$ | (1,756 | ) |
CAR-T Therapeutics | |
| (1,177 | ) | |
| (1,525 | ) |
Other | |
| (18 | ) | |
| (9 | ) |
Total | |
$ | (3,213 | ) | |
$ | (3,290 | ) |
Net income (loss) | |
$ | (3,213 | ) | |
$ | (3,290 | ) |
| |
| | | |
| | |
Total operating costs and expenses | |
$ | 3,386 | | |
$ | 3,609 | |
Less non-cash stock-based compensation | |
| (1,055 | ) | |
| (1,260 | ) |
Operating costs and expenses excluding non-cash stock-based compensation | |
$ | 2,331 | | |
$ | 2,349 | |
Operating costs and expenses excluding non-cash stock-based compensation expense: | |
| | | |
| | |
Cancer Vaccines | |
$ | 1,467 | | |
$ | 1,213 | |
CAR-T Therapeutics | |
| 848 | | |
| 1,128 | |
Other | |
| 16 | | |
| 8 | |
Total | |
$ | 2,331 | | |
$ | 2,349 | |
Operating costs and expenses excluding non-cash share based compensation | |
$ | 2,331 | | |
$ | 2,349 | |
| |
January 31, 2025 | | |
October 31, 2024 | |
Total assets: | |
| | | |
| | |
Cancer Vaccines | |
$ | 11,863 | | |
$ | 12,917 | |
CAR-T Therapeutics | |
| 6,885 | | |
| 8,535 | |
Other | |
| 158 | | |
| 139 | |
Total | |
$ | 18,906 | | |
$ | 21,591 | |
Total assets | |
$ | 18,906 | | |
$ | 21,591 | |
Operating costs and expenses excluding
non-cash stock-based compensation is the measurement the chief operating decision-maker uses in managing the enterprise.
Item 2. Management’s
Discussion and Analysis of Financial Condition and Results of Operations.
Information included in this Quarterly
Report on Form 10-Q (this “Report”) contains forward-looking statements within the meaning of Section 27A of the Securities
Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”). Forward-looking
statements are not statements of historical facts, but rather reflect our current expectations concerning future events and results. We
generally use the words “believes,” “expects,” “intends,” “plans,” “anticipates,”
“likely,” “will” and similar expressions to identify forward-looking statements. Such forward-looking statements,
including those concerning our expectations, involve risks, uncertainties and other factors, some of which are beyond our control, which
may cause our actual results, performance or achievements, or industry results, to be materially different from any future results, performance
or achievements expressed or implied by such forward-looking statements. These risks, uncertainties and factors include, but are not limited
to, those factors set forth in our Annual Report on Form 10-K for the fiscal year ended October 31, 2024. Except as required by applicable law, including the securities laws of the United States,
we undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future
events or otherwise. You are cautioned not to unduly rely on such forward-looking statements when evaluating the information presented
in this Report.
GENERAL
We discuss the description of
our business in the Notes to our Condensed Consolidated Financial Statements.
RESULTS OF OPERATIONS
Three months ended January 31, 2025 compared
with three months ended January 31, 2024
Revenue
We had no revenue during the three-month
periods ended January 31, 2025 and 2024.
We have not generated any revenue
to date from our therapeutics or vaccine programs. In addition, while we pursue our therapeutics and vaccine programs, we may also make
investments in and form new companies to develop additional emerging technologies. We do not expect to begin generating revenue with respect
to any of our current therapy or vaccine programs in the near term. We hope to achieve a profitable outcome by eventually licensing our
technologies to large pharmaceutical companies that have the resources and infrastructure in place to manufacture, market and sell our
technologies as therapeutics or vaccines. The eventual licensing of any of our technologies may take several years, if it is to occur
at all, and may depend on positive results from human clinical trials.
Research and Development
Expenses
During the three months ended
January 31, 2025, research and development expenses related to the development of our cancer vaccines and CAR-T therapeutics consisted
of approximately $975,000 and $577,000, respectively. During the three months ended January 31, 2024 research and development expenses
related to the development of our cancer vaccines and CAR-T therapeutics consisted of approximately $720,000 and $629,000, respectively.
Research and development expenses
increased by approximately $203,000 to approximately $1,552,000 in the three months ended January 31, 2025, from approximately $1,349,000
in the three months ended January 31, 2024. The increase in research and development expenses was primarily due to an increase in outside
research and development expenses related to our breast cancer vaccine program of approximately $88,000, an increase in license fees related
to our ovarian cancer CAR-T therapeutic of approximately $80,000, an increase in employee compensation and related costs, other than stock-based
compensation expense, of approximately $69,000, and an increase in outside research and development expenses related to our new vaccine
discovery program of approximately $56,000, offset by a decrease in employee stock-based compensation expense of approximately $59,000,
and a decrease in consultant stock-based compensation expense of approximately $33,000.
General and Administrative
Expenses
General and administrative expenses
decreased by approximately $426,000 to approximately $1,834,000 in the three months ended January 31, 2025, from approximately $2,260,000
in the three months ended January 31, 2024. The decrease in general and administrative expenses was primarily due to a decrease in investor
and public relations expense of approximately $291,000, a decrease in employee compensation and related costs, other than stock-based
compensation expense, of approximately $70,000, a decrease in director stock-based compensation of approximately $67,000, and a decrease
in legal and other professional fees of approximately $57,000, offset by an increase in employee stock-based compensation expense of approximately
$48,000.
Interest Income
Interest income decreased by approximately
$146,000 to approximately $173,000 in the three months ended January 31, 2025, from approximately $319,000 in the three months ended January
31, 2024, primarily due to a decrease in the amount of short-term investments held and a decrease in interest rates.
Net Loss Attributable to
Noncontrolling Interest
The net loss attributable to noncontrolling
interest, representing Wistar’s ownership interest in Certainty’s net loss, decreased by approximately $6,000 to approximately
$29,000 in the three months ended January 31, 2025 from approximately $35,000 in the three months ended January 31, 2024, as Certainty’s
net loss decreased.
LIQUIDITY AND CAPITAL RESOURCES
Our primary sources of liquidity
are cash, cash equivalents and short-term investments.
Based on currently available information as of March 11, 2025, we believe
that our existing cash, cash equivalents and short-term investments will be sufficient to fund our activities for at least the next twelve
months. The Company had approximately $18,686,000 of total current assets at January 31, 2025 compared to approximately $21,362,000 at
October 31, 2024 which is a reduction of approximately $2,676,000 for the three months ended January 31, 2025. Therefore, the Company
believes that it has sufficient cash, cash equivalents and short-term investments to operate its business, as currently contemplated,
for significantly longer than 12 months from the date of this Report. We have implemented a business model that conserves funds by collaborating
with third parties to develop our technologies. During the three months ended January 31, 2025, we did not issue any shares under our
at-the-market equity offering. Under our at-the-market equity program, which is currently effective and may remain available for us to
use in the future, as of January 31, 2025, we may sell approximately $97 million of common stock.
During the three months ended
January 31, 2025, cash used in operating activities was approximately $2,904,000. Cash provided by investing activities was approximately
$2,703,000, resulting from the maturities of short-term investments of approximately $15,700,000, offset by purchases of short-term investments
totaling approximately $12,997,000. Cash used in financing activities was approximately $17,000, due to expenses related to maintaining
our at-the-market equity offering program. As a result, our cash, cash equivalents, and short-term investments at January 31, 2025 decreased
approximately $2,669,000 to approximately $17,255,000 from approximately $19,924,000 at the end of fiscal year 2024.
CRITICAL ACCOUNTING POLICIES
The Company’s condensed
consolidated financial statements are prepared in conformity with accounting principles generally accepted in the United States of America.
In preparing these financial statements, we make assumptions, judgments and estimates that can have a significant impact on amounts reported
in our condensed consolidated financial statements. We base our assumptions, judgments and estimates on historical experience and various
other factors that we believe to be reasonable under the circumstances. Actual results could differ materially from these estimates under
different assumptions or conditions. On a regular basis, we evaluate our assumptions, judgments and estimates and make changes accordingly.
We believe that, of the significant
accounting policies discussed in Note 2 to our consolidated financial statements in our Annual Report on Form 10-K for the fiscal year
ended October 31, 2024, the following accounting policies require our most difficult, subjective or complex judgments:
|
● |
Revenue Recognition, |
|
● |
Stock-Based Compensation, and |
|
● |
Research and Development Expenses. |
Revenue Recognition
Our revenue has been derived solely
from technology licensing and the sale of patented technologies. Revenue is recognized upon transfer of control of intellectual property
rights and satisfaction of other contractual performance obligations to licensees in an amount that reflects the consideration we expect
to receive.
Our revenue recognition policy
requires us to make certain judgments and estimates in connection with the accounting for revenue. Such areas may include determining
the existence of a contract and identifying each party’s rights and obligations to transfer goods and services, identifying the
performance obligations in the contract, determining the transaction price and allocating the transaction price to separate performance
obligations, estimating the timing of satisfaction of performance obligations, determining whether a promise to grant a license is distinct
from other promised goods or services and evaluating whether a license transfers to a customer at a point in time or over time.
Our revenue arrangements provide
for the payment, within 30 days of execution of the agreement, of contractually determined, one-time, paid-up license fees in settlement
of litigation and in consideration for the grant of certain intellectual property rights for patented technologies owned or controlled
by the Company. These arrangements typically include some combination of the following: (i) the grant of a non-exclusive, retroactive
and future license to manufacture and/or sell products covered by patented technologies owned or controlled by the Company, (ii) a covenant-not-to-sue,
(iii) the release of the licensee from certain claims, and (iv) the dismissal of any pending litigation. In such instances, the intellectual
property rights granted have been perpetual in nature, extending until the expiration of the related patents. Pursuant to the terms of
these agreements, we have no further obligations with respect to the granted intellectual property rights, including no obligation to
maintain or upgrade the technology, or provide future support or services. Licensees obtained control of the intellectual property rights
they have acquired upon execution of the agreement. Accordingly, the performance obligations from these agreements were satisfied and
100% of the revenue was recognized upon the execution of the agreements.
Stock-Based Compensation
The compensation cost for service-based
stock options granted to employees, directors and consultants is measured at the grant date, based on the fair value of the award using
the Black-Scholes pricing model, and is recognized as an expense on a straight-line basis over the requisite service period (the vesting
period of the stock option) which is one to four years. For employee options vesting if the trading price of the Company’s common
stock exceeds certain price targets, we use a Monte Carlo Simulation in estimating the fair value at grant date and recognize compensation
cost over the implied service period.
For stock awards granted to employees
and directors that vest at date of grant we recognize expense based on the grant date market price of the underlying common stock. For
restricted stock awards vesting upon achievement of a price target of our common stock, we use a Monte Carlo Simulation in estimating
the fair value at grant date and recognize compensation cost over the implied service period (median time to vest).
The Black-Scholes pricing model
and the Monte Carlo Simulation we use to estimate fair value requires valuation assumptions of expected term, expected volatility, risk-free
interest rates and expected dividend yield. The expected term of stock options represents the weighted average period the stock options
are expected to remain outstanding. For employees we use the simplified method, which is a weighted average of the vesting term and contractual
term, to determine expected term. The simplified method was adopted since we do not believe that historical experience is representative
of future performance because of the impact of the changes in our operations and the change in terms from historical options. For consultants
we use the contract term for expected term. Under the Black-Scholes pricing model, we estimated the expected volatility of our shares
of common stock based upon the historical volatility of our share price over a period of time equal to the expected term of the grants.
We estimated the risk-free interest rate based on the implied yield available on the applicable grant date of a U.S. Treasury note with
a term equal to the expected term of the underlying grants. We made the dividend yield assumption based on our history of not paying dividends
and our expectation not to pay dividends in the future.
We will reconsider use of the
Black-Scholes pricing model and the Monte Carlo Simulation if additional information becomes available in the future that indicates another
model would be more appropriate. If factors change and we employ different assumptions in future periods, the compensation expense that
we record may differ significantly from what we have recorded in the current period.
Research and Development Expenses
We recognize research and development
expenses as incurred. Advance payments for future research and development activities are deferred and expensed as the services are performed.
We recognize our preclinical studies and clinical trial expenses based on the services performed pursuant to contracts with research institutions,
clinical research organizations (“CROs”), clinical manufacturing organizations (“CMOs”), and other parties that
conduct and manage various stages of research and development activities on our behalf. Fees for such services are recognized based on
management’s estimates after considering the activities and tasks completed by each service provider in a given period, the time
period over which services are expected to be performed, and the level of effort expended in each reporting period.
At each balance sheet date, management
estimates prepaid and accrued research and development costs by discussing progress or stage of completion of activities with internal
personnel and external service providers, and comparing this information to payments made, invoices received, and the agreed-upon contractual
fee to be paid for such services in the applicable contract or statements of work.
In addition, we allocate certain
internal compensation costs to research and development expenses based on management’s estimates of each employee’s time and
effort expended.
EFFECT OF RECENTLY ISSUED PRONOUNCEMENTS
We discuss the effect of recently
issued pronouncements in Note 7 of the condensed consolidated financial statements, included elsewhere in
this Report.
Item 3. Quantitative
and Qualitative Disclosures About Market Risk. Not applicable.
Item 4. Controls
and Procedures.
We carried out an evaluation,
under the supervision and with the participation of our management including our Chief Executive Officer and our Chief Financial Officer,
of the effectiveness of the design and operation of our disclosure controls and procedures pursuant to Rule 13(a)-15(b) of the Exchange
Act. Based upon that evaluation, our Chief Executive Officer and our Chief Financial Officer concluded that our disclosure controls and
procedures are effective as of the end of the period covered by this Report.
There was no change in our internal
control over financial reporting during the three months ended January 31, 2025, that has materially affected, or is reasonably likely
to materially affect, our internal control over financial reporting.
PART II.
OTHER INFORMATION
Item 1. Legal
Proceedings.
Other than lawsuits related to
the enforcement of our patent rights, we are not a party to any material pending legal proceedings, nor are we aware of any pending litigation
or legal proceeding against us that would have a material adverse effect upon our results of operations or financial condition.
Item 1A. Risk
Factors.
There have been no material changes
in our risk factors from those disclosed in our Annual Report on Form 10-K for the fiscal year ended October 31, 2024.
Item 2. Unregistered
Sales of Equity Securities and Use of Proceeds. None.
Item 3. Defaults
Upon Senior Securities. None.
Item 4.
Mine Safety Disclosures. Not Applicable.
Item 5. Other
Information. None.
Item 6. Exhibits.
|
31.1 |
Certification of Chief Executive Officer, pursuant to Section 302 of the Sarbanes-Oxley Act of 2002, dated March 11, 2025. |
|
31.2 |
Certification of Chief Financial Officer, pursuant to Section 302 of the Sarbanes-Oxley Act of 2002, dated March 11, 2025. |
|
32.1 |
Statement of Chief Executive Officer, pursuant to Section 1350 of Title 18 of the United States Code, dated March 11, 2025. |
|
32.2 |
Statement of Chief Financial Officer, pursuant to Section 1350 of Title 18 of the United States Code, dated March 11, 2025. |
|
101.INS |
Inline XBRL Instance Document |
|
101.SCH |
Inline XBRL Taxonomy Extension Schema |
|
101.CAL |
Inline XBRL Taxonomy Extension Calculation Linkbase |
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101.DEF |
Inline XBRL Taxonomy Extension Definition Linkbase |
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Inline XBRL Taxonomy Extension Label Linkbase |
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101.PRE |
Inline XBRL Taxonomy Extension Presentation Linkbase |
|
104 |
Cover Page Interactive Data File (formatted in Inline XBRL and contained in Exhibit 101) |
SIGNATURES
Pursuant to the requirements of
the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto
duly authorized.
|
ANIXA BIOSCIENCES, INC. |
|
|
|
|
By: |
/s/ Dr. Amit Kumar |
|
|
Dr. Amit Kumar |
|
|
Chairman and Chief Executive Officer |
March 11, 2025 |
|
(Principal Executive Officer) |
|
|
|
|
By: |
/s/ Michael J. Catelani |
|
|
Michael J. Catelani |
|
|
President, Chief Operating Officer and |
|
|
Chief Financial Officer |
|
|
(Principal Financial and |
March 11, 2025 |
|
Accounting Officer) |
Exhibit 31.1
CERTIFICATION
I, Dr. Amit Kumar, certify that:
1. |
I have reviewed this quarterly report on Form 10-Q of Anixa Biosciences, Inc.; |
|
|
2. |
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
|
|
3. |
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; |
|
|
4. |
The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
|
(a) |
Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared; |
|
|
|
|
(b) |
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles; |
|
|
|
|
(c) |
Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and |
|
|
|
|
(d) |
Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and |
5. |
The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): |
|
(a) |
All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and |
|
|
|
|
(b) |
Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting. |
|
/s/ Dr. Amit Kumar |
|
Dr. Amit Kumar |
|
Chairman and Chief Executive Officer |
March 11, 2025 |
(Principal Executive Officer) |
Exhibit 31.2
CERTIFICATION
I, Michael J. Catelani, certify that:
1. |
I have reviewed this quarterly report on Form 10-Q of Anixa Biosciences, Inc.; |
|
|
2. |
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
|
|
3. |
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; |
|
|
4. |
The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
|
(a) |
Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared; |
|
|
|
|
(b) |
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles; |
|
|
|
|
(c) |
Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and |
|
|
|
|
(d) |
Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and |
5. |
The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): |
|
(a) |
All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and |
|
|
|
|
(b) |
Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting. |
|
/s/ Michael J. Catelani |
|
Michael J. Catelani |
|
President, Chief Operating Officer and Chief Financial Officer |
March 11, 2025 |
(Principal Financial and Accounting Officer) |
Exhibit 32.1
Statement of Chief Executive Officer
Pursuant to Section 1350 of Title 18 of the United
States Code
Pursuant to Section 1350 of Title 18 of the United
States Code as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned, Dr. Amit Kumar, the Chairman and Chief
Executive Officer of Anixa Biosciences, Inc., hereby certifies that:
|
1. |
The Company’s Form 10-Q Quarterly Report for the period ended January 31, 2025 (the “Report”) fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and |
|
|
|
|
2. |
The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company. |
|
/s/ Dr. Amit Kumar |
|
Dr. Amit Kumar |
|
Chairman and Chief Executive Officer |
March 11, 2025 |
(Principal Executive Officer) |
Exhibit 32.2
Statement of Chief Financial Officer
Pursuant to Section 1350 of Title 18 of the United
States Code
Pursuant to Section 1350 of Title 18 of the United
States Code as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned, Michael J. Catelani, the President,
Chief Operating Officer and Chief Financial Officer of Anixa Biosciences, Inc., hereby certifies that:
|
1. |
The Company’s Form 10-Q Quarterly Report for the period ended January 31, 2025 (the “Report”) fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and |
|
|
|
|
2. |
The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company. |
|
/s/ Michael J. Catelani |
|
Michael J. Catelani |
|
President, Chief Operating Officer and Chief Financial Officer |
March 11, 2025 |
(Principal Financial and Accounting Officer) |
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v3.25.0.1
Condensed Consolidated Balance Sheets (Unaudited) - USD ($)
|
Jan. 31, 2025 |
Oct. 31, 2024 |
Current assets: |
|
|
Cash and cash equivalents |
$ 1,053,000
|
$ 1,271,000
|
Short-term investments |
16,202,000
|
18,653,000
|
Receivables |
|
173,000
|
Prepaid expenses and other current assets |
1,431,000
|
1,265,000
|
Total current assets |
18,686,000
|
21,362,000
|
Operating lease right-of-use asset |
220,000
|
229,000
|
Total assets |
18,906,000
|
21,591,000
|
Current liabilities: |
|
|
Accounts payable |
600,000
|
525,000
|
Accrued expenses |
1,363,000
|
1,946,000
|
Operating lease liability |
36,000
|
29,000
|
Total current liabilities |
1,999,000
|
2,500,000
|
Operating lease liability, non-current |
194,000
|
203,000
|
Total liabilities |
2,193,000
|
2,703,000
|
Commitments and contingencies (Note 10) |
|
|
Shareholders’ equity: |
|
|
Preferred stock, value |
|
|
Common stock, par value $.01 per share; 100,000,000 shares authorized; 32,196,862 shares issued and outstanding as of January 31, 2025 and October 31, 2024 |
322,000
|
322,000
|
Additional paid-in capital |
261,470,000
|
260,432,000
|
Accumulated deficit |
(243,934,000)
|
(240,750,000)
|
Treasury stock, 2,000 shares at cost |
(6,000)
|
(6,000)
|
Total shareholders’ equity |
17,852,000
|
19,998,000
|
Noncontrolling interest (Note 2) |
(1,139,000)
|
(1,110,000)
|
Total equity |
16,713,000
|
18,888,000
|
Total liabilities and equity |
18,906,000
|
21,591,000
|
Series A Convertible Preferred Stock [Member] |
|
|
Shareholders’ equity: |
|
|
Preferred stock, value |
|
|
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v3.25.0.1
Condensed Consolidated Balance Sheets (Unaudited) (Parenthetical) - $ / shares
|
Jan. 31, 2025 |
Oct. 31, 2024 |
Preferred stock, par value |
$ 100
|
$ 100
|
Preferred stock, shares authorized |
19,860
|
19,860
|
Preferred stock, shares issued |
0
|
0
|
Preferred stock, shares outstanding |
0
|
0
|
Common stock, par value |
$ 0.01
|
$ 0.01
|
Common stock, shares authorized |
100,000,000
|
100,000,000
|
Common stock, shares issued |
32,196,862
|
32,196,862
|
Common stock, shares outstanding |
32,196,862
|
32,196,862
|
Treasury stock, common shares |
2,000
|
2,000
|
Series A Convertible Preferred Stock [Member] |
|
|
Preferred stock, par value |
$ 100
|
$ 100
|
Preferred stock, shares authorized |
140
|
140
|
Preferred stock, shares issued |
0
|
0
|
Preferred stock, shares outstanding |
0
|
0
|
X |
- DefinitionFace amount or stated value per share of common stock.
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v3.25.0.1
Condensed Consolidated Statements of Operations (Unaudited) - USD ($) shares in Thousands, $ in Thousands |
3 Months Ended |
Jan. 31, 2025 |
Jan. 31, 2024 |
Income Statement [Abstract] |
|
|
Revenue |
|
|
Operating costs and expenses: |
|
|
Research and development expenses (including non-cash stock-based compensation expenses of $397 and $489, respectively) |
1,552
|
1,349
|
General and administrative expenses (including non-cash stock-based compensation expenses of $658 and $771, respectively) |
1,834
|
2,260
|
Total operating costs and expenses |
3,386
|
3,609
|
Loss from operations |
(3,386)
|
(3,609)
|
Interest income |
173
|
319
|
Net loss |
(3,213)
|
(3,290)
|
Less: Net loss attributable to noncontrolling interest |
(29)
|
(35)
|
Net loss attributable to common shareholders |
$ (3,184)
|
$ (3,255)
|
Net loss per common share attributable to common shareholders: |
|
|
Basic |
$ (0.10)
|
$ (0.10)
|
Diluted |
$ (0.10)
|
$ (0.10)
|
Weighted average common shares outstanding: |
|
|
Basic |
32,197
|
31,446
|
Diluted |
32,197
|
31,446
|
X |
- DefinitionTotal costs of sales and operating expenses for the period.
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v3.25.0.1
Condensed Consolidated Statements of Equity (Unaudited) - USD ($)
|
Total |
Common Stock [Member] |
Additional Paid-in Capital [Member] |
Retained Earnings [Member] |
Treasury Stock, Common [Member] |
Parent [Member] |
Noncontrolling Interest [Member] |
Balance at Oct. 31, 2023 |
$ 23,371,000
|
$ 311,000
|
$ 252,222,000
|
$ (228,196,000)
|
|
$ 24,337,000
|
$ (966,000)
|
Balance, shares at Oct. 31, 2023 |
|
31,145,219
|
|
|
|
|
|
Stock option compensation to employees and directors |
1,108,000
|
|
1,108,000
|
|
|
1,108,000
|
|
Stock options issued to consultants |
56,000
|
|
56,000
|
|
|
56,000
|
|
Common stock issued to consultants |
96,000
|
$ 1,000
|
95,000
|
|
|
96,000
|
|
Common stock issued to consultants, shares |
|
29,336
|
|
|
|
|
|
Common stock issued in an at-the-market offering, net of offering expenses of $68 |
2,196,000
|
$ 6,000
|
2,190,000
|
|
|
2,196,000
|
|
Common stock issued in an at-the-market offering, net of offering expenses of $68, shares |
|
555,820
|
|
|
|
|
|
Common stock issued upon exercise of stock options |
67,000
|
|
67,000
|
|
|
67,000
|
|
Common stock issued upon exercise of stock options, shares |
|
24,000
|
|
|
|
|
|
Net loss |
(3,290,000)
|
|
|
(3,255,000)
|
|
(3,255,000)
|
(35,000)
|
Balance at Jan. 31, 2024 |
23,604,000
|
$ 318,000
|
255,738,000
|
(231,451,000)
|
|
24,605,000
|
(1,001,000)
|
Balance, shares at Jan. 31, 2024 |
|
31,754,375
|
|
|
|
|
|
Balance at Oct. 31, 2024 |
18,888,000
|
$ 322,000
|
260,432,000
|
(240,750,000)
|
$ (6,000)
|
19,998,000
|
(1,110,000)
|
Balance, shares at Oct. 31, 2024 |
|
32,196,862
|
|
|
|
|
|
Stock option compensation to employees and directors |
1,031,000
|
|
1,031,000
|
|
|
1,031,000
|
|
Stock options issued to consultants |
24,000
|
|
24,000
|
|
|
24,000
|
|
Expenses related to an at-the-market offering |
(17,000)
|
|
(17,000)
|
|
|
(17,000)
|
|
Net loss |
(3,213,000)
|
|
|
(3,184,000)
|
|
(3,184,000)
|
(29,000)
|
Balance at Jan. 31, 2025 |
$ 16,713,000
|
$ 322,000
|
$ 261,470,000
|
$ (243,934,000)
|
$ (6,000)
|
$ 17,852,000
|
$ (1,139,000)
|
Balance, shares at Jan. 31, 2025 |
|
32,196,862
|
|
|
|
|
|
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Condensed Consolidated Statements of Cash Flows (Unaudited) - USD ($) $ in Thousands |
3 Months Ended |
Jan. 31, 2025 |
Jan. 31, 2024 |
Reconciliation of net loss to net cash used in operating activities: |
|
|
Net loss |
$ (3,213)
|
$ (3,290)
|
Stock option compensation to employees and directors |
1,031
|
1,108
|
Stock options issued to consultants |
24
|
56
|
Common stock issued to consultants |
|
96
|
Amortization of operating lease right-of-use asset |
9
|
13
|
Amortization of discount on held-to-maturity securities |
(252)
|
|
Change in operating assets and liabilities: |
|
|
Receivables |
173
|
(121)
|
Prepaid expenses and other current assets |
(166)
|
212
|
Accounts payable |
75
|
158
|
Accrued expenses |
(583)
|
(528)
|
Operating lease liability |
(2)
|
(13)
|
Net cash used in operating activities |
(2,904)
|
(2,309)
|
Cash flows from investing activities: |
|
|
Disbursements to acquire short-term investments |
(12,997)
|
(20,020)
|
Proceeds from maturities of short-term investments |
15,700
|
20,149
|
Net cash provided by investing activities |
2,703
|
129
|
Cash flows from financing activities: |
|
|
Net (expenses) proceeds from an at-the-market offering |
(17)
|
2,196
|
Proceeds from exercise of stock options |
|
67
|
Net cash (used in) provided by financing activities |
(17)
|
2,263
|
Net (decrease) increase in cash and cash equivalents |
(218)
|
83
|
Cash and cash equivalents at beginning of period |
1,271
|
915
|
Cash and cash equivalents at end of period |
$ 1,053
|
$ 998
|
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v3.25.0.1
BUSINESS AND FUNDING
|
3 Months Ended |
Jan. 31, 2025 |
Organization, Consolidation and Presentation of Financial Statements [Abstract] |
|
BUSINESS AND FUNDING |
1. BUSINESS AND FUNDING
Description of Business
As used herein, “we,”
“us,” “our,” the “Company” or “Anixa” means Anixa Biosciences, Inc. and its consolidated
subsidiaries.
Anixa Biosciences, Inc. is a biotechnology
company developing therapies and vaccines that are focused on critical unmet needs in oncology. Our therapeutics program consists of the
development of a chimeric endocrine receptor-T cell therapy, a novel form of chimeric antigen receptor-T cell (“CAR-T”) technology,
initially focused on treating ovarian cancer, which is being developed at our subsidiary, Certainty Therapeutics, Inc. (“Certainty”).
Our vaccine programs include (i) the development of a vaccine against breast cancer, initially focused on triple negative breast cancer
(“TNBC”), the most lethal form of breast cancer, (ii) the development of a vaccine against ovarian cancer, and (iii) a vaccine
discovery program utilizing the same mechanism as our breast and ovarian cancer vaccines, to develop additional cancer vaccines to address
many intractable cancers, including high incidence malignancies in lung, colon and prostate.
Our subsidiary, Certainty, is
developing immuno-therapy drugs against cancer. Certainty holds an exclusive worldwide, royalty-bearing license to use certain intellectual
property owned or controlled by The Wistar Institute (“Wistar”), the nation’s first independent biomedical research
institute and a leading NCI designated cancer research center, relating to Wistar’s chimeric endocrine receptor targeted therapy
technology. We have initially focused on the development of a treatment for ovarian cancer, but we also may pursue applications of the
technology for the development of treatments for additional solid tumors. The license agreement requires Certainty to make certain cash
and equity payments to Wistar upon achievement of specific development milestones. With respect to Certainty’s equity obligations
to Wistar, Certainty issued to Wistar shares of its common stock equal to five percent (5%) of the common stock of Certainty, such equity
stake subject to dilution by further funding of Certainty’s activities by the Company. Due to such Company funding, Wistar’s
equity stake in Certainty was 4.3% as of January 31, 2025.
Certainty, in collaboration with
the H. Lee Moffitt Cancer Center and Research Institute, Inc. (“Moffitt”), has begun human clinical testing of the CAR-T technology
licensed by Certainty from Wistar aimed initially at treating ovarian cancer. After receiving authorization from the FDA, we commenced
enrollment of patients in a Phase 1 clinical trial and treated the first patient in August 2022. Further, in May 2023 and August 2023,
we treated the second and third patients in the trial, respectively, at the same dose level as the first patient, and the treatment was
well-tolerated by the patients. In February 2024, May 2024 and June 2024, we treated the three patients, respectively, of the second dose
cohort, where the patients were administered a three-times higher dose of cells than the patients in the first cohort. The treatment at
this dose level has also been well-tolerated by the patients. While the dose levels in the first two cohorts were expected to be sub-therapeutic,
two of the six patients exhibited some anecdotal signs of efficacy. Both have shown possible signs of tumor necrosis, and one is still
alive nearly 2 years past initial treatment. In the case of this patient, due to the encouraging results with her initial treatment, we
sought single patient Investigational New Drug (“IND”) application permission from the FDA to re-dose her. This re-dosing
was approved by the FDA, and we administered her second treatment in October 2024. This second treatment appears to have been well-tolerated
by the patient. From November 2024 to February 2025, we treated three patients in the third dose cohort, where they were administered
a ten-times higher dose of cells than the patients in the first dose cohort. Consistent with the lower dose cohorts, the treatment appears
to have been well-tolerated by the patients. As of March 11, 2025, we are preparing to enroll patients in the 4th dose cohort,
where we will be administering a 30-times higher dose than the original dose cohort.
This study is a dose-escalation
trial with two arms based on route of delivery—intraperitoneal or intravenous—to determine the maximum tolerated dose in patients
with recurrent epithelial ovarian cancer and to assess persistence, expansion and efficacy of the modified T cells. The study is being
conducted at Moffitt and will consist of up to 24 to 48 patients who have received at least two prior lines of chemotherapy. The study
is estimated to be completed in two to three years depending on multiple factors including when the maximum tolerated dose is reached,
the rate of patient enrollment, the significance of efficacy data and how long we maintain the two different delivery methods.
We hold an exclusive worldwide,
royalty-bearing license to use certain intellectual property owned or controlled by The Cleveland Clinic Foundation (“Cleveland
Clinic”) relating to certain breast cancer vaccine technology developed at Cleveland Clinic. The license agreement requires us to
make certain cash payments to Cleveland Clinic upon achievement of specific development milestones. Utilizing this technology, we are
working in collaboration with Cleveland Clinic to develop a method to vaccinate women against breast cancer, focused initially on TNBC.
The focus of this vaccine is a specific protein, α-lactalbumin, that is only expressed during lactation in a healthy woman’s
mammary tissue. This protein disappears when the woman is no longer lactating, but reappears in many forms of breast cancer, especially
TNBC. Studies have shown that vaccinating against this protein prevents breast cancer in mice.
In October 2021, following the
U.S. Food and Drug Administration’s (“FDA”) authorization to proceed, we commenced dosing patients in a Phase 1 clinical
trial of our breast cancer vaccine. This study, which is being fully funded by a U.S. Department of Defense grant to Cleveland Clinic,
is a multiple-ascending dose Phase 1 trial to determine the maximum tolerated dose (“MTD”) of the vaccine in patients with
early-stage, triple-negative breast cancer as well as monitor immune response. The study is being conducted at Cleveland Clinic. During
the course of the Phase 1 study, participants will receive three vaccinations, each two weeks apart, and will be closely monitored for
side effects and immune response. The first segment of the study, Phase 1a, will consist of approximately 24 patients who have completed
treatment for early-stage, triple-negative breast cancer within the past three years and are currently tumor-free but at high risk for
recurrence. Studies show that 42% of TNBC patients will have a recurrence of their cancer, with most of the recurrences occurring in the
first two to three years after standard of care treatment. In January 2023, the number of participants in each dose cohort was expanded,
and as of August 2023, we had completed vaccinating all patients in these expanded cohorts. In December 2023, we presented the immunological
data collected to date at the San Antonio Breast Cancer Symposium. The data presented show that in the vaccinated women who had been tested
to date, various levels of antigen-specific T cell responses were observed at all dose levels. Subsequently, we began vaccinating participants
in additional dose cohorts at varying dose levels of the different key components of the vaccine. Further, in November 2023, we commenced
vaccination of participants in the second segment of the trial, Phase 1b, that includes participants who have never had cancer, but carry
certain mutations in genes such as BRCA1, BRCA2 or PALB2, that indicate a greater risk of developing TNBC in the future, and have elected
to have a prophylactic mastectomy. Finally, in January 2024, we commenced vaccination of participants in the third segment of the trial,
Phase 1c, that includes post-operative TNBC patients that have residual disease following treatment and are currently undergoing treatment
with pembrolizumab (Keytruda®). In November 2024, we presented the most recent data from each of the three arms of the trial at the
Society for Immunotherapy of Cancer (SITC) Annual Meeting. Key findings presented include i) patients exhibited antigen-specific immune
responses at all dose levels and in all three patient groups (Phase 1a, 1b and 1c), ii) patients receiving our vaccine in combination
with Keytruda are not showing any additional or more severe adverse side effects, and iii) no adverse side effects were seen other than
varying degrees of injection site irritation. These findings are promising, and as we continue the Phase 1 trial, we are preparing to
initiate a Phase 2 clinical trial in the neo-adjuvant setting (pre-surgery) to determine possible therapeutic effect of the vaccine. We
anticipate commencing the Phase 2 trial in 2025.
We hold an exclusive worldwide,
royalty-bearing license to use certain intellectual property owned or controlled by Cleveland Clinic relating to certain ovarian cancer
vaccine technology. The license agreement requires us to make certain cash payments to Cleveland Clinic upon achievement of specific development
milestones. This technology pertains to among other things, the use of vaccines for the treatment or prevention of ovarian cancers which
express the anti-Mullerian hormone receptor 2 protein containing an extracellular domain (“AMHR2-ED”). In healthy tissue,
this protein regulates growth and development of egg-containing follicles in the ovary. While expression of AMHR2-ED naturally and markedly
declines during menopause, this protein is expressed at high levels in the ovaries of postmenopausal women with ovarian cancer. Researchers
at Cleveland Clinic believe that a vaccine targeting AMHR2-ED could prevent the occurrence of ovarian cancer.
In May 2021, Cleveland Clinic
was granted acceptance for our ovarian cancer vaccine technology into the National Cancer Institute’s (“NCI”) PREVENT
program. The NCI is a part of the National Institutes of Health (“NIH”). The PREVENT program is a peer-reviewed agent development
program designed to support pre-clinical development of innovative interventions and biomarkers for cancer prevention and interception
towards clinical trials. The scientific and financial resources of the PREVENT program are being used for our ovarian cancer vaccine technology
to perform virtually all pre-clinical research and development, manufacturing and IND enabling studies. This work is being performed at
NCI facilities, by NCI scientific staff and with NCI financial resources and will require no material financial expenditures by the Company,
nor the payment of any future consideration by the Company to NCI.
In May 2024, based on the positive
clinical results to date in the development of our breast cancer vaccine, we entered into a Joint Development and Option Agreement with
Cleveland Clinic to collaborate in efforts to develop additional vaccines for the prevention or treatment of cancers. Working with Cleveland
Clinic researchers, we are focusing on the same novel scientific mechanism as in our breast and ovarian cancer vaccines, and working to
discover additional retired proteins that may be associated with other forms of cancer, specifically high incidence malignancies in the
lung, colon and prostate.
Over the next several quarters,
we expect the development of our therapeutics and vaccines to be the primary focus of the Company. As part of our legacy operations, the
Company remains engaged in limited patent licensing activities of its various patent portfolios. We do not expect these activities to
be a significant part of the Company’s ongoing operations nor do we expect these activities to require material financial resources
or attention of senior management.
Over the past several years, our
revenue was derived from technology licensing and the sale of patented technologies, including revenue from the settlement of litigation.
We have not generated any revenue to date from our vaccine or therapeutics programs. In addition, while we pursue our vaccine and therapeutics
programs, we may also make investments in and form new companies to develop additional emerging technologies. We do not expect to begin
generating revenue with respect to any of our current vaccine or therapy programs in the near term. We hope to achieve a profitable outcome
by eventually licensing our technologies to large pharmaceutical companies that have the resources and infrastructure in place to manufacture,
market and sell our technologies as vaccines or therapeutics. The eventual licensing of any of our technologies may take several years,
if it is to occur at all, and may depend on positive results from human clinical trials.
Funding and Management’s Plans
Based on currently available information as of March 11, 2025, we believe
that our existing cash, cash equivalents and short-term investments will be sufficient to fund our activities for at least the next twelve
months. The Company had approximately $18,686,000 of total current assets at January 31, 2025 compared to approximately $21,362,000 at
October 31, 2024 which is a reduction of approximately $2,676,000 for the three months ended January 31, 2025. Therefore, the Company
believes that it has sufficient cash, cash equivalents and short-term investments to operate its business, as currently contemplated,
for significantly longer than 12 months from the date of this Report. We have implemented a business model that conserves funds by collaborating
with third parties to develop our technologies. During the three months ended January 31, 2025, we did not issue any shares under our
at-the-market equity offering. Under our at-the-market equity program, which is currently effective and may remain available for us to
use in the future, as of January 31, 2025, we may sell approximately $97 million of common stock.
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v3.25.0.1
SIGNIFICANT ACCOUNTING POLICIES
|
3 Months Ended |
Jan. 31, 2025 |
Accounting Policies [Abstract] |
|
SIGNIFICANT ACCOUNTING POLICIES |
2. SIGNIFICANT ACCOUNTING POLICIES
Basis of Presentation
The accompanying unaudited condensed
consolidated financial statements have been prepared in accordance with generally accepted accounting principles in the United States
of America (“US GAAP”) for interim financial information and with the instructions to Form 10-Q and Rule 8-03 of Regulation
S-X. Accordingly, certain information and disclosures required by generally accepted accounting principles in annual financial statements
have been omitted or condensed. These interim condensed consolidated financial statements should be read in conjunction with the audited
consolidated financial statements and related disclosures included in our Annual Report on Form 10-K for the fiscal year ended October
31, 2024. The accompanying October 31, 2024 condensed consolidated balance sheet data was derived from the audited financial statements
but does not include all disclosures required by US GAAP. The condensed consolidated financial statements include all adjustments of a
normal recurring nature which, in the opinion of management, are necessary for a fair statement of our financial position as of January
31, 2025, and results of operations and cash flows for the interim periods represented. The results of operations for the three months
ended January 31, 2025 are not necessarily indicative of the results to be expected for the year.
Noncontrolling Interest
Noncontrolling interest represents
Wistar’s equity ownership in Certainty and is presented as a component of equity. The following table sets forth the changes in
noncontrolling interest for the three months ended January 31, 2025 (in thousands):
SCHEDULE OF CHANGES IN NONCONTROLLING INTEREST
Balance, October 31, 2024 | |
$ | (1,110 | ) |
Net loss attributable to noncontrolling interest | |
| (29 | ) |
Balance, January 31, 2025 | |
$ | (1,139 | ) |
Revenue Recognition
Our revenue
has been derived solely from technology licensing and the sale of patented technologies. Revenue is recognized upon transfer of control
of intellectual property rights and satisfaction of other contractual performance obligations to licensees in an amount that reflects
the consideration we expect to receive.
Our revenue
recognition policy requires us to make certain judgments and estimates in connection with the accounting for revenue. Such areas may include
determining the existence of a contract and identifying each party’s rights and obligations to transfer goods and services, identifying
the performance obligations in the contract, determining the transaction price and allocating the transaction price to separate performance
obligations, estimating the timing of satisfaction of performance obligations, determining whether a promise to grant a license is distinct
from other promised goods or services and evaluating whether a license transfers to a customer at a point in time or over time.
Our revenue
arrangements provide for the payment, within 30 days of execution of the agreement, of contractually determined, one-time, paid-up license
fees in settlement of litigation and in consideration for the grant of certain intellectual property rights for patented technologies
owned or controlled by the Company. These arrangements typically include some combination of the following: (i) the grant of a non-exclusive,
retroactive and future license to manufacture and/or sell products covered by patented technologies owned or controlled by the Company,
(ii) a covenant-not-to-sue, (iii) the release of the licensee from certain claims, and (iv) the dismissal of any pending litigation. In
such instances, the intellectual property rights granted have been perpetual in nature, extending until the expiration of the related
patents. Pursuant to the terms of these agreements, we have no further obligations with respect to the granted intellectual property rights,
including no obligation to maintain or upgrade the technology, or provide future support or services. Licensees obtained control of the
intellectual property rights they have acquired upon execution of the agreement. Accordingly, the performance obligations from these agreements
were satisfied and 100% of the revenue was recognized upon the execution of the agreements.
Cost of Revenues
Cost of revenues include the costs
and expenses incurred in connection with our patent licensing and enforcement activities, including inventor royalties paid to original
patent owners, contingent legal fees paid to external counsel, other patent-related legal expenses paid to external counsel, licensing
and enforcement related research and consulting and other expenses paid to third-parties. These costs are included under the caption “Operating
costs and expenses” in the accompanying consolidated statements of operations.
Research and Development Expenses
Research and development expenses
consist primarily of employee compensation, payments to third parties for research and development activities and other direct costs associated
with developing our therapeutics and vaccines. We recognize research and development expenses as incurred. Advance payments for future
research and development activities are deferred and expensed as the services are performed. We recognize our preclinical studies and
clinical trial expenses based on the services performed pursuant to contracts with research institutions, clinical research organizations
(“CROs”), clinical manufacturing organizations (“CMOs”), and other parties that conduct and manage various stages
of research and development activities on our behalf. Fees for such services are recognized based on management’s estimates after
considering the activities and tasks completed by each service provider in a given period, the time period over which services are expected
to be performed, and the level of effort expended in each reporting period.
At each
balance sheet date, management estimates prepaid and accrued research and development costs by discussing progress or stage of completion
of activities with internal personnel and external service providers, and comparing this information to payments made, invoices received,
and the agreed-upon contractual fee to be paid for such services in the applicable contract or statements of work.
In addition,
we allocate certain internal compensation costs to research and development expenses based on management’s estimates of each employee’s
time and effort expended.
Investment Policy
The Company’s investment
policy is designed to optimize returns while managing risk and liquidity. The policy allows for investments in a diversified range of
financial instruments, including U.S. government debt securities with fixed maturities and contractual cash flows, as well as alternative
investments such as Bitcoin and Bitcoin-based exchange traded funds (collectively, the “Bitcoin Assets”).
The Company acquires U.S. government
debt securities that it has the positive intent and ability to hold to maturity. These securities are recorded at amortized cost, net
of any applicable discount which is amortized to interest income, and are accounted for as held-to-maturity securities. The Company’s
Bitcoin Assets are measured at fair value based on quoted prices on active exchanges. The Company recognizes changes in the fair value
of Bitcoin Assets as gains or losses in the statement of operations during the period in which they occur.
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v3.25.0.1
STOCK-BASED COMPENSATION
|
3 Months Ended |
Jan. 31, 2025 |
Share-Based Payment Arrangement [Abstract] |
|
STOCK-BASED COMPENSATION |
3. STOCK-BASED COMPENSATION
The Company maintains stock equity
incentive plans under which the Company may grant incentive stock options, non-qualified stock options, stock appreciation rights, stock
awards, performance awards, or stock units to employees, directors and consultants.
Stock Option Compensation Expense
We account for stock options granted
to employees, directors and consultants using the accounting guidance in ASC 718, Stock Compensation. We estimate the fair value of service-based
stock options on the date of grant, using the Black-Scholes pricing model, and recognize compensation expense over the requisite service
period of the grant. We recorded stock-based compensation expense related to service-based stock options granted to employees and directors
of approximately $1,031,000 and $1,108,000 during the three months ended January 31, 2025 and 2024.
The compensation cost for service-based
stock options granted to consultants is measured at the grant date, based on the fair value of the award using the Black-Scholes pricing
model, and is expensed on a straight-line basis over the requisite service period (the vesting period of the stock option) which is one
to three years. We recorded stock-based consulting expense related to stock options granted to consultants of approximately $24,000 and
$56,000 during the three months ended January 31, 2025 and 2024, respectively.
Stock Option Activity
During the three months ended
January 31, 2025 and 2024, we granted options to purchase 1,355,000 shares and 1,335,000 shares of common stock, respectively, to employees
and consultants, with exercise prices ranging from $2.37 to $4.39 per share, pursuant to the 2018 Share Plan. During the three months
ended January 31, 2025, no stock options were exercised. During the three months ended January 31, 2024, stock options to purchase 24,000
shares of common stock were exercised on a cash basis, with aggregate proceeds of approximately $67,000.
Stock Option Plans
During the three months ended
January 31, 2025, we had two stock option plans: the Anixa Biosciences, Inc. 2010 Share Incentive Plan (the “2010 Share Plan”)
and the Anixa Biosciences, Inc. 2018 Share Incentive Plan (the “2018 Share Plan”), which were adopted by our Board of Directors
on July 14, 2010 and January 25, 2018, respectively. The 2018 Share Plan was approved by our shareholders on March 29, 2018.
2010 Share Plan
The 2010 Share Plan provided for
the grant of nonqualified stock options, stock appreciation rights, stock awards, performance awards and stock units to employees, directors
and consultants. In accordance with the provisions of the 2010 Share Plan, the plan terminated with respect to the ability to grant future
awards on July 14, 2020. Information regarding the 2010 Share Plan for the three months ended January 31, 2025 is as follows:
SCHEDULE OF OPTION ACTIVITY
| |
Shares | | |
Weighted Average Exercise Price Per Share | | |
Aggregate Intrinsic Value (in thousands) | |
Options outstanding at October 31, 2024 | |
| 986,968 | | |
$ | 2.77 | | |
| | |
Options outstanding and exercisable at January 31, 2025 | |
| 986,968 | | |
$ | 2.77 | | |
$ | 566 | |
The following table summarizes
information about stock options outstanding and exercisable under the 2010 Share Plan as of January 31, 2025:
SCHEDULE
OF OPTIONS OUTSTANDING AND EXERCISABLE
Range of
Exercise Prices |
|
|
Number
Outstanding and
Exercisable |
|
|
Weighted Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
0.67 - $2.27 |
|
|
|
316,000 |
|
|
|
2.5 |
|
|
$ |
1.11 |
|
$ |
2.58 - $3.13 |
|
|
|
251,968 |
|
|
|
1.1 |
|
|
$ |
2.93 |
|
$ |
3.46 - $5.30 |
|
|
|
419,000 |
|
|
|
3.2 |
|
|
$ |
3.93 |
|
2018 Share Plan
The 2018 Share Plan provides for
the grant of incentive stock options, nonqualified stock options, stock appreciation rights, stock awards, performance awards and stock
units to employees, directors and consultants. As of January 31, 2025, the 2018 Share Plan had 645,000 shares available for future grants.
Information regarding the 2018 Share Plan for the three months ended January 31, 2025 is as follows:
SCHEDULE
OF OPTION ACTIVITY
|
|
Shares |
|
|
Weighted
Average Exercise
Price Per Share |
|
|
Aggregate
Intrinsic Value
(in thousands) |
|
Options outstanding at October 31, 2024 |
|
|
11,171,094 |
|
|
$ |
3.74 |
|
|
|
|
|
Granted |
|
|
1,355,000 |
|
|
|
2.37 |
|
|
|
|
|
Forfeited/expired |
|
|
(25,000 |
) |
|
|
3.96 |
|
|
|
|
|
Options outstanding at January 31, 2025 |
|
|
12,501,094 |
|
|
$ |
3.59 |
|
|
$ |
1,093 |
|
Options exercisable at January 31, 2025 |
|
|
8,260,549 |
|
|
$ |
3.56 |
|
|
$ |
391 |
|
The following table summarizes
information about stock options outstanding and exercisable under the 2018 Share Plan as of January 31, 2025:
SCHEDULE
OF OPTIONS OUTSTANDING AND EXERCISABLE
|
|
|
Options Outstanding |
|
|
Options Exercisable |
|
Range of
Exercise Prices |
|
|
Number
Outstanding |
|
|
Weighted
Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
|
Number
Exercisable |
|
|
Weighted
Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
2.09 - $3.87 |
|
|
|
6,663,879 |
|
|
|
6.5 |
|
|
$ |
3.06 |
|
|
|
5,168,886 |
|
|
|
5.5 |
|
|
$ |
3.22 |
|
$ |
4.02 - $5.30 |
|
|
|
5,837,215 |
|
|
|
7.4 |
|
|
$ |
4.20 |
|
|
|
3,091,663 |
|
|
|
7.2 |
|
|
$ |
4.13 |
|
Employee Stock Purchase Plan
The Company maintains the Anixa
Biosciences, Inc. Employee Stock Purchase Plan (the “ESPP”) which permits eligible employees to purchase shares at not less
than 85% of the market value of the Company’s common stock on the offering date or the purchase date of the applicable offering
period, whichever is lower. The ESPP was adopted by our Board of Directors on August 13, 2018 and approved by our shareholders on September
27, 2018. During the three months ended January 31, 2025 and 2024, no shares were purchased under the ESPP.
Warrants
As of January 31, 2025, we had
warrants outstanding to purchase 300,000 shares of common stock at $6.56 per share, issued during fiscal year 2021 and expiring on March
22, 2026.
Information regarding the Company’s
warrants for the three months ended January 31, 2025 is as follows:
SCHEDULE
OF WARRANTS ACTIVITY
|
|
Shares |
|
|
Weighted
Average Exercise
Price Per Share |
|
|
Aggregate
Intrinsic
Value |
|
Warrants outstanding at October 31, 2024 |
|
|
300,000 |
|
|
$ |
6.56 |
|
|
|
|
|
Warrants outstanding and exercisable at January 31, 2025 |
|
|
300,000 |
|
|
$ |
6.56 |
|
|
$ |
0 |
|
The following table summarizes
information about the Company’s outstanding and exercisable warrants as of January 31, 2025:
SCHEDULE OF OUTSTANDING AND EXERCISABLE
Range of
Exercise Prices |
|
|
Number
Outstanding and
Exercisable |
|
|
Weighted Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
6.56 |
|
|
|
300,000 |
|
|
|
1.1 |
|
|
$ |
6.56 |
|
Stock Awards
During the three months ended
January 31, 2025, we did not issue any stock awards. During the three months ended January 31, 2024, we issued 29,336 shares of common
stock to consultants providing investor relations services, and recorded expense of approximately $96,000.
Treasury stock
As of January 31, 2025, the Company
held 2,000 shares of its common stock as treasury stock. These shares were repurchased during the fiscal year ended October 31, 2024,
at an average cost of $3.17 per share for a total cost of approximately $6,000. The repurchases were made as part of a stock buyback program
approved by our Board of Directors on July 11, 2024. The treasury shares are accounted for under the cost method and are recorded as a
reduction in shareholders’ equity in the consolidated balance sheet. The Company may reissue treasury shares for stock option exercises,
acquisitions, or other corporate purposes.
|
X |
- DefinitionTabular disclosure of share-based payment arrangement.
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v3.25.0.1
FAIR VALUE MEASUREMENTS
|
3 Months Ended |
Jan. 31, 2025 |
Fair Value Disclosures [Abstract] |
|
FAIR VALUE MEASUREMENTS |
4. FAIR VALUE MEASUREMENTS
US GAAP defines fair value and
establishes a framework for measuring fair value. We have categorized our financial assets and liabilities, based on the priority of the
inputs to the valuation technique, into a three-level fair value hierarchy as set forth below. If the inputs used to measure the financial
instruments fall within different levels of the hierarchy, the categorization is based on the lowest level input that is significant to
the fair value measurement of the instrument.
Financial assets and liabilities
recorded in the accompanying condensed consolidated balance sheets are categorized based on the inputs to the valuation techniques as
follows:
Level 1 – Financial instruments
whose values are based on unadjusted quoted prices for identical assets or liabilities in an active market which we have the ability to
access at the measurement date.
Level 2 – Financial instruments
whose values are based on quoted market prices in markets where trading occurs infrequently or whose values are based on quoted prices
of instruments with similar attributes in active markets.
Level 3 – Financial instruments
whose values are based on prices or valuation techniques that require inputs that are both unobservable and significant to the overall
fair value measurement. These inputs reflect management’s own assumptions about the assumptions a market participant would use in
pricing the instrument.
The following table presents the
hierarchy for our financial assets measured at fair value on a recurring basis as of January 31, 2025 (in thousands):
SCHEDULE OF FINANCIAL ASSETS MEASURED AT FAIR VALUE ON A RECURRING BASIS
| |
Level 1 | | |
Level 2 | | |
Level 3 | | |
Total | |
Money market funds: | |
| | | |
| | | |
| | | |
| | |
Cash equivalents | |
$ | 912 | | |
$ | - | | |
$ | - | | |
$ | 912 | |
Bitcoin exchange traded funds: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 10 | | |
| - | | |
| 10 | |
U.S. treasury bills: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 16,192 | | |
| - | | |
| 16,192 | |
Total financial assets | |
$ | 912 | | |
$ | 16,202 | | |
$ | - | | |
$ | 17,114 | |
The following table presents the
hierarchy for our financial assets measured at fair value on a recurring basis as of October 31, 2024 (in thousands):
| |
Level 1 | | |
Level 2 | | |
Level 3 | | |
Total | |
Money market funds: | |
| | | |
| | | |
| | | |
| | |
Cash equivalents | |
$ | 1,170 | | |
$ | - | | |
$ | - | | |
$ | 1,170 | |
U.S. treasury bills: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 18,653 | | |
| - | | |
| 18,653 | |
Total financial assets | |
$ | 1,170 | | |
$ | 18,653 | | |
$ | - | | |
$ | 19,823 | |
Our non-financial assets that
are measured at fair value on a non-recurring basis are property and equipment and other assets which are measured using fair value techniques
whenever events or changes in circumstances indicate a condition of impairment exists. The estimated fair value of prepaid expenses and
other current assets, accounts payable and accrued expenses approximates their individual carrying amounts due to the short-term nature
of these measurements. Cash equivalents are stated at carrying value which approximates fair value.
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v3.25.0.1
ACCRUED EXPENSES
|
3 Months Ended |
Jan. 31, 2025 |
Payables and Accruals [Abstract] |
|
ACCRUED EXPENSES |
5. ACCRUED EXPENSES
Accrued expenses consist of the
following as of:
SCHEDULE OF ACCRUED EXPENSES
| |
January 31, | | |
October 31, | |
| |
2025 | | |
2024 | |
| |
(in thousands) | |
Payroll and related expenses | |
$ | 515 | | |
$ | 1,126 | |
Accrued royalty and contingent legal fees | |
| 626 | | |
| 626 | |
Accrued other | |
| 222 | | |
| 194 | |
Accrued expenses | |
$ | 1,363 | | |
$ | 1,946 | |
|
X |
- DefinitionThe entire disclosure for accounts payable and accrued liabilities at the end of the reporting period.
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v3.25.0.1
NET LOSS PER SHARE OF COMMON STOCK
|
3 Months Ended |
Jan. 31, 2025 |
Net loss per common share attributable to common shareholders: |
|
NET LOSS PER SHARE OF COMMON STOCK |
6. NET LOSS PER SHARE OF COMMON STOCK
Basic net loss per common share
(“Basic EPS”) is computed by dividing net loss by the weighted average number of common shares outstanding. Diluted net loss
per common share (“Diluted EPS”) is computed by dividing net loss by the weighted average number of common shares and dilutive
common share equivalents and convertible securities then outstanding. Diluted EPS for all periods presented is the same as Basic EPS,
as the inclusion of the effect of common share equivalents then outstanding would be anti-dilutive. For this reason, excluded from the
calculation of Diluted EPS for the three months ended January 31, 2025 and 2024, were stock options to purchase 13,488,062 and 12,497,094
shares, respectively, and warrants to purchase 300,000 and 300,000 shares, respectively.
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v3.25.0.1
EFFECT OF RECENTLY ADOPTED AND ISSUED PRONOUNCEMENTS
|
3 Months Ended |
Jan. 31, 2025 |
Effect Of Recently Adopted And Issued Pronouncements |
|
EFFECT OF RECENTLY ADOPTED AND ISSUED PRONOUNCEMENTS |
7. EFFECT OF RECENTLY ADOPTED AND ISSUED PRONOUNCEMENTS
In November 2023, the FASB issued
Accounting Standards Update 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, to provide more disaggregated
expense information about a public entity’s reportable segments. The amendments in this update should be applied retrospectively
and are effective for fiscal years beginning after December 15, 2023, and interim periods beginning after December 15, 2024. We began
a detailed assessment of the impact that this guidance will have on our consolidated financial statements and related disclosures, and
our analysis is currently ongoing.
In December 2023, the FASB issued
Accounting Standards Update 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, to require disaggregated information
about a reporting entity’s effective tax rate reconciliation as well as information on income taxes paid. The amendments in this
update should be applied prospectively, with an option to apply them retrospectively, and are effective for fiscal years beginning after
December 15, 2024 for public entities. We began a detailed assessment of the impact that this guidance will have on our consolidated financial
statements and related disclosures, and our analysis is currently ongoing.
In March 2024, the FASB issued
Accounting Standards Update 2024-03, Income Statement—Reporting Comprehensive Income—Expense Disaggregation Disclosures (Subtopic
220-40): Disaggregation of Income Statement Expenses, to improve the disclosures about a public business entity’s expenses and to
provide more detailed information about the types of expenses in commonly presented expense captions. The amendments in this update should
be applied either prospectively or retrospectively, and are effective for fiscal years beginning after December 15, 2026, and interim
periods beginning after December 15, 2027. We began a detailed assessment of the impact that this guidance will have on our consolidated
financial statements and related disclosures, and our analysis is currently ongoing.
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v3.25.0.1
INCOME TAXES
|
3 Months Ended |
Jan. 31, 2025 |
Income Tax Disclosure [Abstract] |
|
INCOME TAXES |
8. INCOME TAXES
We recognize deferred tax assets
and liabilities for the estimated future tax effects of events that have been recognized in our financial statements or tax returns. Under
this method, deferred tax assets and liabilities are determined based on the difference between the financial statement and tax bases
of assets and liabilities using enacted tax rates in effect in the years in which the differences are expected to reverse. A valuation
allowance is established, when necessary, to reduce deferred tax assets to the amount expected to be realized. We have provided a full
valuation allowance against our deferred tax asset due to our historical pre-tax losses and the uncertainty regarding the realizability
of these deferred tax assets.
We have substantial net operating
loss carryforwards for Federal and California income tax returns. These net operating loss carryforwards could be subject to limitations
under Internal Revenue Code section 382, the effects of which have not been determined by the Company. We have no unrecognized income
tax benefits as of January 31, 2025 and October 31, 2024 and we account for interest and penalties related to income tax matters, if any,
in general and administrative expenses.
|
X |
- DefinitionThe entire disclosure for income tax.
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v3.25.0.1
LEASES
|
3 Months Ended |
Jan. 31, 2025 |
Leases |
|
LEASES |
9. LEASES
We lease approximately 2,000 square
feet of office space at 3150 Almaden Expressway, San Jose, California (our principal executive offices) from an unrelated party pursuant
to an operating lease that, as amended, will expire on September 30, 2027, with an option to extend the lease an additional two years.
The base rent is approximately $5,000 per month and the lease provides for annual increases of approximately 3% and an escalation clause
for increases in certain operating costs. The lease, as amended, resulted in a right-of-use asset and lease liability of approximately
$250,000 with a discount rate of 12%. Rent expense was approximately $16,000 and $17,000, respectively, for the three months ended January
31, 2025 and 2024.
For operating leases, the lease
liability is initially and subsequently measured at the present value of the unpaid lease payments. The remaining 56-month lease term
as of January 31, 2025 for the Company’s lease includes the noncancelable period of the lease and the additional two-year option
period that the Company is reasonably certain to exercise. All right-of-use assets are reviewed for impairment when indications of impairment
are present.
As of January 31, 2025, the annual
minimum future lease payments of our operating lease liability were as follows (in thousands):
SCHEDULE OF MINIMUM LEASE PAYMENTS
For Years Ended October 31, | |
Operating Leases | |
2025 (remaining) | |
$ | 47 | |
2026 | |
| 63 | |
2027 | |
| 64 | |
2028 | |
| 66 | |
2029 | |
| 63 | |
Total future minimum lease payments, undiscounted | |
| 303 | |
Less: Imputed interest | |
| 73 | |
Present value of future minimum lease payments | |
$ | 230 | |
| |
| | |
Balance as of January 31, 2025: | |
| | |
Operating lease liability | |
$ | 36 | |
Operating lease liability, non-current | |
| 194 | |
Total | |
$ | 230 | |
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v3.25.0.1
COMMITMENTS AND CONTINGENCES
|
3 Months Ended |
Jan. 31, 2025 |
Commitments and Contingencies Disclosure [Abstract] |
|
COMMITMENTS AND CONTINGENCES |
10. COMMITMENTS AND CONTINGENCES
Litigation Matters
Other than lawsuits related to
the enforcement of our patent rights, we are not a party to any material pending legal proceedings, nor are we aware of any pending litigation
or legal proceeding against us that would have a material adverse effect upon our results of operations or financial condition.
License Commitments
As of January 31, 2025, our commitments
under certain technology license agreements related to our therapeutic and vaccine development programs for the next twelve months, were
approximately $150,000.
Research & Development Agreements
We have entered into certain research
and development agreements with various collaboration partners and third-party vendors related to i) the manufacturing of materials necessary
for the expected Phase 2 clinical trial of our breast cancer vaccine, ii) the discovery of new vaccine targets in high incidence malignancies
in prostate, lung and colon and iii) the further development of our CAR-T technology. As of January 31, 2025, future payments the Company
may make under these agreements, dependent upon, among other things, development of analytical methods, formulation feasibility studies,
stability testing and results of manufacturing processes, may be approximately $3.7 million and such payments may be made over up to a
five-year period.
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v3.25.0.1
SEGMENT INFORMATION
|
3 Months Ended |
Jan. 31, 2025 |
Segment Reporting [Abstract] |
|
SEGMENT INFORMATION |
11. SEGMENT INFORMATION
We follow the accounting guidance
of ASC 280 “Segment Reporting” (“ASC 280”). Reportable operating segments are determined based on the management
approach. The management approach, as defined by ASC 280, is based on the way that the chief operating decision-maker organizes the segments
within an enterprise for making operating decisions and assessing performance. While our results of operations are primarily reviewed
on a consolidated basis, the chief operating decision-maker manages the enterprise in three reportable segments, each with different operating and potential revenue generating
characteristics: (i) Cancer Vaccines, (ii) CAR-T Therapeutics, and (iii) Other. The following represents selected financial information
for our segments for the three months ended January 31, 2025 and 2024 and as of January 31, 2025 and October 31, 2024 (in thousands):
SCHEDULE OF SEGMENT INFORMATION
| |
2025 | | |
2024 | |
| |
For the Three Months Ended January 31, | |
| |
2025 | | |
2024 | |
Net loss: | |
| | | |
| | |
Cancer Vaccines | |
$ | (2,018 | ) | |
$ | (1,756 | ) |
CAR-T Therapeutics | |
| (1,177 | ) | |
| (1,525 | ) |
Other | |
| (18 | ) | |
| (9 | ) |
Total | |
$ | (3,213 | ) | |
$ | (3,290 | ) |
Net income (loss) | |
$ | (3,213 | ) | |
$ | (3,290 | ) |
| |
| | | |
| | |
Total operating costs and expenses | |
$ | 3,386 | | |
$ | 3,609 | |
Less non-cash stock-based compensation | |
| (1,055 | ) | |
| (1,260 | ) |
Operating costs and expenses excluding non-cash stock-based compensation | |
$ | 2,331 | | |
$ | 2,349 | |
Operating costs and expenses excluding non-cash stock-based compensation expense: | |
| | | |
| | |
Cancer Vaccines | |
$ | 1,467 | | |
$ | 1,213 | |
CAR-T Therapeutics | |
| 848 | | |
| 1,128 | |
Other | |
| 16 | | |
| 8 | |
Total | |
$ | 2,331 | | |
$ | 2,349 | |
Operating costs and expenses excluding non-cash share based compensation | |
$ | 2,331 | | |
$ | 2,349 | |
| |
January 31, 2025 | | |
October 31, 2024 | |
Total assets: | |
| | | |
| | |
Cancer Vaccines | |
$ | 11,863 | | |
$ | 12,917 | |
CAR-T Therapeutics | |
| 6,885 | | |
| 8,535 | |
Other | |
| 158 | | |
| 139 | |
Total | |
$ | 18,906 | | |
$ | 21,591 | |
Total assets | |
$ | 18,906 | | |
$ | 21,591 | |
Operating costs and expenses excluding
non-cash stock-based compensation is the measurement the chief operating decision-maker uses in managing the enterprise.
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v3.25.0.1
SIGNIFICANT ACCOUNTING POLICIES (Policies)
|
3 Months Ended |
Jan. 31, 2025 |
Accounting Policies [Abstract] |
|
Basis of Presentation |
Basis of Presentation
The accompanying unaudited condensed
consolidated financial statements have been prepared in accordance with generally accepted accounting principles in the United States
of America (“US GAAP”) for interim financial information and with the instructions to Form 10-Q and Rule 8-03 of Regulation
S-X. Accordingly, certain information and disclosures required by generally accepted accounting principles in annual financial statements
have been omitted or condensed. These interim condensed consolidated financial statements should be read in conjunction with the audited
consolidated financial statements and related disclosures included in our Annual Report on Form 10-K for the fiscal year ended October
31, 2024. The accompanying October 31, 2024 condensed consolidated balance sheet data was derived from the audited financial statements
but does not include all disclosures required by US GAAP. The condensed consolidated financial statements include all adjustments of a
normal recurring nature which, in the opinion of management, are necessary for a fair statement of our financial position as of January
31, 2025, and results of operations and cash flows for the interim periods represented. The results of operations for the three months
ended January 31, 2025 are not necessarily indicative of the results to be expected for the year.
|
Noncontrolling Interest |
Noncontrolling Interest
Noncontrolling interest represents
Wistar’s equity ownership in Certainty and is presented as a component of equity. The following table sets forth the changes in
noncontrolling interest for the three months ended January 31, 2025 (in thousands):
SCHEDULE OF CHANGES IN NONCONTROLLING INTEREST
Balance, October 31, 2024 | |
$ | (1,110 | ) |
Net loss attributable to noncontrolling interest | |
| (29 | ) |
Balance, January 31, 2025 | |
$ | (1,139 | ) |
|
Revenue Recognition |
Revenue Recognition
Our revenue
has been derived solely from technology licensing and the sale of patented technologies. Revenue is recognized upon transfer of control
of intellectual property rights and satisfaction of other contractual performance obligations to licensees in an amount that reflects
the consideration we expect to receive.
Our revenue
recognition policy requires us to make certain judgments and estimates in connection with the accounting for revenue. Such areas may include
determining the existence of a contract and identifying each party’s rights and obligations to transfer goods and services, identifying
the performance obligations in the contract, determining the transaction price and allocating the transaction price to separate performance
obligations, estimating the timing of satisfaction of performance obligations, determining whether a promise to grant a license is distinct
from other promised goods or services and evaluating whether a license transfers to a customer at a point in time or over time.
Our revenue
arrangements provide for the payment, within 30 days of execution of the agreement, of contractually determined, one-time, paid-up license
fees in settlement of litigation and in consideration for the grant of certain intellectual property rights for patented technologies
owned or controlled by the Company. These arrangements typically include some combination of the following: (i) the grant of a non-exclusive,
retroactive and future license to manufacture and/or sell products covered by patented technologies owned or controlled by the Company,
(ii) a covenant-not-to-sue, (iii) the release of the licensee from certain claims, and (iv) the dismissal of any pending litigation. In
such instances, the intellectual property rights granted have been perpetual in nature, extending until the expiration of the related
patents. Pursuant to the terms of these agreements, we have no further obligations with respect to the granted intellectual property rights,
including no obligation to maintain or upgrade the technology, or provide future support or services. Licensees obtained control of the
intellectual property rights they have acquired upon execution of the agreement. Accordingly, the performance obligations from these agreements
were satisfied and 100% of the revenue was recognized upon the execution of the agreements.
|
Cost of Revenues |
Cost of Revenues
Cost of revenues include the costs
and expenses incurred in connection with our patent licensing and enforcement activities, including inventor royalties paid to original
patent owners, contingent legal fees paid to external counsel, other patent-related legal expenses paid to external counsel, licensing
and enforcement related research and consulting and other expenses paid to third-parties. These costs are included under the caption “Operating
costs and expenses” in the accompanying consolidated statements of operations.
|
Research and Development Expenses |
Research and Development Expenses
Research and development expenses
consist primarily of employee compensation, payments to third parties for research and development activities and other direct costs associated
with developing our therapeutics and vaccines. We recognize research and development expenses as incurred. Advance payments for future
research and development activities are deferred and expensed as the services are performed. We recognize our preclinical studies and
clinical trial expenses based on the services performed pursuant to contracts with research institutions, clinical research organizations
(“CROs”), clinical manufacturing organizations (“CMOs”), and other parties that conduct and manage various stages
of research and development activities on our behalf. Fees for such services are recognized based on management’s estimates after
considering the activities and tasks completed by each service provider in a given period, the time period over which services are expected
to be performed, and the level of effort expended in each reporting period.
At each
balance sheet date, management estimates prepaid and accrued research and development costs by discussing progress or stage of completion
of activities with internal personnel and external service providers, and comparing this information to payments made, invoices received,
and the agreed-upon contractual fee to be paid for such services in the applicable contract or statements of work.
In addition,
we allocate certain internal compensation costs to research and development expenses based on management’s estimates of each employee’s
time and effort expended.
|
Investment Policy |
Investment Policy
The Company’s investment
policy is designed to optimize returns while managing risk and liquidity. The policy allows for investments in a diversified range of
financial instruments, including U.S. government debt securities with fixed maturities and contractual cash flows, as well as alternative
investments such as Bitcoin and Bitcoin-based exchange traded funds (collectively, the “Bitcoin Assets”).
The Company acquires U.S. government
debt securities that it has the positive intent and ability to hold to maturity. These securities are recorded at amortized cost, net
of any applicable discount which is amortized to interest income, and are accounted for as held-to-maturity securities. The Company’s
Bitcoin Assets are measured at fair value based on quoted prices on active exchanges. The Company recognizes changes in the fair value
of Bitcoin Assets as gains or losses in the statement of operations during the period in which they occur.
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v3.25.0.1
SIGNIFICANT ACCOUNTING POLICIES (Tables)
|
3 Months Ended |
Jan. 31, 2025 |
Accounting Policies [Abstract] |
|
SCHEDULE OF CHANGES IN NONCONTROLLING INTEREST |
Noncontrolling interest represents
Wistar’s equity ownership in Certainty and is presented as a component of equity. The following table sets forth the changes in
noncontrolling interest for the three months ended January 31, 2025 (in thousands):
SCHEDULE OF CHANGES IN NONCONTROLLING INTEREST
Balance, October 31, 2024 | |
$ | (1,110 | ) |
Net loss attributable to noncontrolling interest | |
| (29 | ) |
Balance, January 31, 2025 | |
$ | (1,139 | ) |
|
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v3.25.0.1
STOCK-BASED COMPENSATION (Tables)
|
3 Months Ended |
Jan. 31, 2025 |
Warrant [Member] |
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
SCHEDULE OF WARRANTS ACTIVITY |
Information regarding the Company’s
warrants for the three months ended January 31, 2025 is as follows:
SCHEDULE
OF WARRANTS ACTIVITY
|
|
Shares |
|
|
Weighted
Average Exercise
Price Per Share |
|
|
Aggregate
Intrinsic
Value |
|
Warrants outstanding at October 31, 2024 |
|
|
300,000 |
|
|
$ |
6.56 |
|
|
|
|
|
Warrants outstanding and exercisable at January 31, 2025 |
|
|
300,000 |
|
|
$ |
6.56 |
|
|
$ |
0 |
|
|
SCHEDULE OF OUTSTANDING AND EXERCISABLE |
The following table summarizes
information about the Company’s outstanding and exercisable warrants as of January 31, 2025:
SCHEDULE OF OUTSTANDING AND EXERCISABLE
Range of
Exercise Prices |
|
|
Number
Outstanding and
Exercisable |
|
|
Weighted Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
6.56 |
|
|
|
300,000 |
|
|
|
1.1 |
|
|
$ |
6.56 |
|
|
2010 Share Plan [Member] |
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
SCHEDULE OF OPTION ACTIVITY |
SCHEDULE OF OPTION ACTIVITY
| |
Shares | | |
Weighted Average Exercise Price Per Share | | |
Aggregate Intrinsic Value (in thousands) | |
Options outstanding at October 31, 2024 | |
| 986,968 | | |
$ | 2.77 | | |
| | |
Options outstanding and exercisable at January 31, 2025 | |
| 986,968 | | |
$ | 2.77 | | |
$ | 566 | |
|
SCHEDULE OF OPTIONS OUTSTANDING AND EXERCISABLE |
The following table summarizes
information about stock options outstanding and exercisable under the 2010 Share Plan as of January 31, 2025:
SCHEDULE
OF OPTIONS OUTSTANDING AND EXERCISABLE
Range of
Exercise Prices |
|
|
Number
Outstanding and
Exercisable |
|
|
Weighted Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
0.67 - $2.27 |
|
|
|
316,000 |
|
|
|
2.5 |
|
|
$ |
1.11 |
|
$ |
2.58 - $3.13 |
|
|
|
251,968 |
|
|
|
1.1 |
|
|
$ |
2.93 |
|
$ |
3.46 - $5.30 |
|
|
|
419,000 |
|
|
|
3.2 |
|
|
$ |
3.93 |
|
|
2018 Share Plan [Member] |
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
SCHEDULE OF OPTION ACTIVITY |
SCHEDULE
OF OPTION ACTIVITY
|
|
Shares |
|
|
Weighted
Average Exercise
Price Per Share |
|
|
Aggregate
Intrinsic Value
(in thousands) |
|
Options outstanding at October 31, 2024 |
|
|
11,171,094 |
|
|
$ |
3.74 |
|
|
|
|
|
Granted |
|
|
1,355,000 |
|
|
|
2.37 |
|
|
|
|
|
Forfeited/expired |
|
|
(25,000 |
) |
|
|
3.96 |
|
|
|
|
|
Options outstanding at January 31, 2025 |
|
|
12,501,094 |
|
|
$ |
3.59 |
|
|
$ |
1,093 |
|
Options exercisable at January 31, 2025 |
|
|
8,260,549 |
|
|
$ |
3.56 |
|
|
$ |
391 |
|
|
SCHEDULE OF OPTIONS OUTSTANDING AND EXERCISABLE |
The following table summarizes
information about stock options outstanding and exercisable under the 2018 Share Plan as of January 31, 2025:
SCHEDULE
OF OPTIONS OUTSTANDING AND EXERCISABLE
|
|
|
Options Outstanding |
|
|
Options Exercisable |
|
Range of
Exercise Prices |
|
|
Number
Outstanding |
|
|
Weighted
Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
|
Number
Exercisable |
|
|
Weighted
Average
Remaining
Contractual Life
(in years) |
|
|
Weighted
Average
Exercise Price |
|
$ |
2.09 - $3.87 |
|
|
|
6,663,879 |
|
|
|
6.5 |
|
|
$ |
3.06 |
|
|
|
5,168,886 |
|
|
|
5.5 |
|
|
$ |
3.22 |
|
$ |
4.02 - $5.30 |
|
|
|
5,837,215 |
|
|
|
7.4 |
|
|
$ |
4.20 |
|
|
|
3,091,663 |
|
|
|
7.2 |
|
|
$ |
4.13 |
|
|
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v3.25.0.1
FAIR VALUE MEASUREMENTS (Tables)
|
3 Months Ended |
Jan. 31, 2025 |
Fair Value Disclosures [Abstract] |
|
SCHEDULE OF FINANCIAL ASSETS MEASURED AT FAIR VALUE ON A RECURRING BASIS |
The following table presents the
hierarchy for our financial assets measured at fair value on a recurring basis as of January 31, 2025 (in thousands):
SCHEDULE OF FINANCIAL ASSETS MEASURED AT FAIR VALUE ON A RECURRING BASIS
| |
Level 1 | | |
Level 2 | | |
Level 3 | | |
Total | |
Money market funds: | |
| | | |
| | | |
| | | |
| | |
Cash equivalents | |
$ | 912 | | |
$ | - | | |
$ | - | | |
$ | 912 | |
Bitcoin exchange traded funds: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 10 | | |
| - | | |
| 10 | |
U.S. treasury bills: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 16,192 | | |
| - | | |
| 16,192 | |
Total financial assets | |
$ | 912 | | |
$ | 16,202 | | |
$ | - | | |
$ | 17,114 | |
The following table presents the
hierarchy for our financial assets measured at fair value on a recurring basis as of October 31, 2024 (in thousands):
| |
Level 1 | | |
Level 2 | | |
Level 3 | | |
Total | |
Money market funds: | |
| | | |
| | | |
| | | |
| | |
Cash equivalents | |
$ | 1,170 | | |
$ | - | | |
$ | - | | |
$ | 1,170 | |
U.S. treasury bills: | |
| | | |
| | | |
| | | |
| | |
Short-term investments | |
| - | | |
| 18,653 | | |
| - | | |
| 18,653 | |
Total financial assets | |
$ | 1,170 | | |
$ | 18,653 | | |
$ | - | | |
$ | 19,823 | |
|
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v3.25.0.1
ACCRUED EXPENSES (Tables)
|
3 Months Ended |
Jan. 31, 2025 |
Payables and Accruals [Abstract] |
|
SCHEDULE OF ACCRUED EXPENSES |
Accrued expenses consist of the
following as of:
SCHEDULE OF ACCRUED EXPENSES
| |
January 31, | | |
October 31, | |
| |
2025 | | |
2024 | |
| |
(in thousands) | |
Payroll and related expenses | |
$ | 515 | | |
$ | 1,126 | |
Accrued royalty and contingent legal fees | |
| 626 | | |
| 626 | |
Accrued other | |
| 222 | | |
| 194 | |
Accrued expenses | |
$ | 1,363 | | |
$ | 1,946 | |
|
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v3.25.0.1
LEASES (Tables)
|
3 Months Ended |
Jan. 31, 2025 |
Leases |
|
SCHEDULE OF MINIMUM LEASE PAYMENTS |
As of January 31, 2025, the annual
minimum future lease payments of our operating lease liability were as follows (in thousands):
SCHEDULE OF MINIMUM LEASE PAYMENTS
For Years Ended October 31, | |
Operating Leases | |
2025 (remaining) | |
$ | 47 | |
2026 | |
| 63 | |
2027 | |
| 64 | |
2028 | |
| 66 | |
2029 | |
| 63 | |
Total future minimum lease payments, undiscounted | |
| 303 | |
Less: Imputed interest | |
| 73 | |
Present value of future minimum lease payments | |
$ | 230 | |
| |
| | |
Balance as of January 31, 2025: | |
| | |
Operating lease liability | |
$ | 36 | |
Operating lease liability, non-current | |
| 194 | |
Total | |
$ | 230 | |
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v3.25.0.1
SEGMENT INFORMATION (Tables)
|
3 Months Ended |
Jan. 31, 2025 |
Segment Reporting [Abstract] |
|
SCHEDULE OF SEGMENT INFORMATION |
SCHEDULE OF SEGMENT INFORMATION
| |
2025 | | |
2024 | |
| |
For the Three Months Ended January 31, | |
| |
2025 | | |
2024 | |
Net loss: | |
| | | |
| | |
Cancer Vaccines | |
$ | (2,018 | ) | |
$ | (1,756 | ) |
CAR-T Therapeutics | |
| (1,177 | ) | |
| (1,525 | ) |
Other | |
| (18 | ) | |
| (9 | ) |
Total | |
$ | (3,213 | ) | |
$ | (3,290 | ) |
Net income (loss) | |
$ | (3,213 | ) | |
$ | (3,290 | ) |
| |
| | | |
| | |
Total operating costs and expenses | |
$ | 3,386 | | |
$ | 3,609 | |
Less non-cash stock-based compensation | |
| (1,055 | ) | |
| (1,260 | ) |
Operating costs and expenses excluding non-cash stock-based compensation | |
$ | 2,331 | | |
$ | 2,349 | |
Operating costs and expenses excluding non-cash stock-based compensation expense: | |
| | | |
| | |
Cancer Vaccines | |
$ | 1,467 | | |
$ | 1,213 | |
CAR-T Therapeutics | |
| 848 | | |
| 1,128 | |
Other | |
| 16 | | |
| 8 | |
Total | |
$ | 2,331 | | |
$ | 2,349 | |
Operating costs and expenses excluding non-cash share based compensation | |
$ | 2,331 | | |
$ | 2,349 | |
| |
January 31, 2025 | | |
October 31, 2024 | |
Total assets: | |
| | | |
| | |
Cancer Vaccines | |
$ | 11,863 | | |
$ | 12,917 | |
CAR-T Therapeutics | |
| 6,885 | | |
| 8,535 | |
Other | |
| 158 | | |
| 139 | |
Total | |
$ | 18,906 | | |
$ | 21,591 | |
Total assets | |
$ | 18,906 | | |
$ | 21,591 | |
|
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v3.25.0.1
BUSINESS AND FUNDING (Details Narrative) - USD ($)
|
3 Months Ended |
|
Jan. 31, 2025 |
Oct. 31, 2024 |
Total current assets |
$ 18,686,000
|
$ 21,362,000
|
Reduction, current assets |
2,676,000
|
|
Common Stock [Member] |
|
|
Value of additional shares available for sale |
$ 97,000,000
|
|
The Wistar Institute [Member] |
|
|
Percentage of common stock issued |
5.00%
|
|
Equity stake percentage |
4.30%
|
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v3.25.0.1
SCHEDULE OF OPTION ACTIVITY (Details) $ / shares in Units, $ in Thousands |
3 Months Ended |
Jan. 31, 2025
USD ($)
$ / shares
shares
|
2010 Share Plan [Member] |
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
Shares, Options outstanding | shares |
986,968
|
Weighted Average Exercise Price Per Share, Outstanding Beginning balance | $ / shares |
$ 2.77
|
Shares, Options outstanding, Ending balance | shares |
986,968
|
Shares, Options outstanding, Exercisable | shares |
986,968
|
Shares, Options outstanding, Ending balance | $ / shares |
$ 2.77
|
Weighted Average Exercise Price Per Share, Exercisable | $ / shares |
$ 2.77
|
Aggregate Intrinsic Value, Outstanding Ending balance | $ |
$ 566
|
Aggregate Intrinsic Value, Exercisable | $ |
$ 566
|
2018 Share Plan [Member] |
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
Shares, Options outstanding | shares |
11,171,094
|
Weighted Average Exercise Price Per Share, Outstanding Beginning balance | $ / shares |
$ 3.74
|
Shares, Options outstanding, Ending balance | shares |
12,501,094
|
Shares, Options outstanding, Exercisable | shares |
8,260,549
|
Shares, Options outstanding, Ending balance | $ / shares |
$ 3.59
|
Weighted Average Exercise Price Per Share, Exercisable | $ / shares |
$ 3.56
|
Aggregate Intrinsic Value, Outstanding Ending balance | $ |
$ 1,093
|
Aggregate Intrinsic Value, Exercisable | $ |
$ 391
|
Shares, Granted | shares |
1,355,000
|
Shares, options, granted | $ / shares |
$ 2.37
|
Shares, options, forfeited or expired | shares |
(25,000)
|
Weighted average price per share, forfeited or expired | $ / shares |
$ 3.96
|
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v3.25.0.1
SCHEDULE OF OPTIONS OUTSTANDING AND EXERCISABLE (Details) - $ / shares
|
3 Months Ended |
|
Jan. 31, 2025 |
Oct. 31, 2024 |
2010 Share Plan [Member] |
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
Number of outstanding |
986,968
|
986,968
|
Weighted average exercise price |
$ 2.77
|
$ 2.77
|
Number exercisable, options exercisable |
986,968
|
|
Weighted average exercise price, options exercisable |
$ 2.77
|
|
2010 Share Plan [Member] | Range One [Member] |
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
Range of exercise prices, lower limit |
0.67
|
|
Range of exercise prices, upper limit |
$ 2.27
|
|
Number of Outstanding |
316,000
|
|
Number of Exercisable |
316,000
|
|
Weighted Average Remaining Contractual Life |
2 years 6 months
|
|
Weighted Average Exercise Price |
$ 1.11
|
|
2010 Share Plan [Member] | Range Two [Member] |
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
Range of exercise prices, lower limit |
2.58
|
|
Range of exercise prices, upper limit |
$ 3.13
|
|
Number of Outstanding |
251,968
|
|
Number of Exercisable |
251,968
|
|
Weighted Average Remaining Contractual Life |
1 year 1 month 6 days
|
|
Weighted Average Exercise Price |
$ 2.93
|
|
2010 Share Plan [Member] | Range Three [Member] |
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
Range of exercise prices, lower limit |
3.46
|
|
Range of exercise prices, upper limit |
$ 5.30
|
|
Number of Outstanding |
419,000
|
|
Number of Exercisable |
419,000
|
|
Weighted Average Remaining Contractual Life |
3 years 2 months 12 days
|
|
Weighted Average Exercise Price |
$ 3.93
|
|
2018 Share Plan [Member] |
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
Number of outstanding |
12,501,094
|
11,171,094
|
Weighted average exercise price |
$ 3.59
|
$ 3.74
|
Number exercisable, options exercisable |
8,260,549
|
|
Weighted average exercise price, options exercisable |
$ 3.56
|
|
2018 Share Plan [Member] | Range One [Member] |
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
Range of exercise prices, lower limit |
2.09
|
|
Range of exercise prices, upper limit |
$ 3.87
|
|
Number of outstanding |
6,663,879
|
|
Weighted average remaining contractual life |
6 years 6 months
|
|
Weighted average exercise price |
$ 3.06
|
|
Number exercisable, options exercisable |
5,168,886
|
|
Weighted average remaining contractual life (in years), options exercisable |
5 years 6 months
|
|
Weighted average exercise price, options exercisable |
$ 3.22
|
|
2018 Share Plan [Member] | Range Two [Member] |
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
Range of exercise prices, lower limit |
4.02
|
|
Range of exercise prices, upper limit |
$ 5.30
|
|
Number of outstanding |
5,837,215
|
|
Weighted average remaining contractual life |
7 years 4 months 24 days
|
|
Weighted average exercise price |
$ 4.20
|
|
Number exercisable, options exercisable |
3,091,663
|
|
Weighted average remaining contractual life (in years), options exercisable |
7 years 2 months 12 days
|
|
Weighted average exercise price, options exercisable |
$ 4.13
|
|
X |
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v3.25.0.1
SCHEDULE OF WARRANTS ACTIVITY (Details) - Warrant [Member] $ / shares in Units, $ in Thousands |
Jan. 31, 2025
USD ($)
$ / shares
shares
|
Shares, Warrants outstanding | shares |
300,000
|
Weighted Average Exercise Price Per Share, Warrants outstanding | $ / shares |
$ 6.56
|
Shares, Warrants outstanding | shares |
300,000
|
Shares, Warrants exercisable | shares |
300,000
|
Weighted Average Exercise Price Per Share, Warrants outstanding | $ / shares |
$ 6.56
|
Weighted Average Exercise Price Per Share, Warrants, exercisable | $ / shares |
$ 6.56
|
Aggregate intrinsic value, Warrants outstanding | $ |
$ 0
|
Aggregate intrinsic value, Warrants exercisable | $ |
$ 0
|
X |
- DefinitionNumber of equity instruments other than options exercisable, including both vested and non-vested instruments.
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STOCK-BASED COMPENSATION (Details Narrative) - USD ($)
|
3 Months Ended |
|
Jan. 31, 2025 |
Jan. 31, 2024 |
Oct. 31, 2024 |
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Proceeds from options exercised |
|
$ 67,000
|
|
Expenses for shares issued services |
|
$ 96,000
|
|
Treasury stock, common shares |
2,000
|
|
2,000
|
Treasury stock repurchased, average cost |
$ 3.17
|
|
|
Treasury stock total cost |
$ 6,000
|
|
$ 6,000
|
Warrant [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Class of Warrant or Right, Number of Securities Called by Warrants or Rights |
300,000
|
|
|
Class of Warrant or Right, Exercise Price of Warrants or Rights |
$ 6.56
|
|
|
Warrants and Rights Outstanding, Maturity Date |
Mar. 22, 2026
|
|
|
Share-Based Payment Arrangement, Option [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Common stock issued upon exercise of stock options |
|
24,000
|
|
Proceeds from options exercised |
|
$ 67,000
|
|
2018 Share Plan [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Shares options, granted |
1,355,000
|
|
|
Shares available for future grants |
645,000
|
|
|
Employee Stock Purchase Plan [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Employees purchase shares percentage |
85.00%
|
|
|
Shares purchased |
0
|
0
|
|
Employees and Directors [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Options granted |
$ 1,031,000
|
$ 1,108,000
|
|
Consultants [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Options granted |
$ 24,000
|
$ 56,000
|
|
Employees And Consultants [Member] | 2018 Share Plan [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Shares options, granted |
1,355,000
|
1,335,000
|
|
Employees And Consultants [Member] | 2018 Share Plan [Member] | Minimum [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Share exercise price |
$ 2.37
|
|
|
Employees And Consultants [Member] | 2018 Share Plan [Member] | Maximum [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Share exercise price |
$ 4.39
|
|
|
Consultant [Member] |
|
|
|
Share-Based Compensation Arrangement by Share-Based Payment Award [Line Items] |
|
|
|
Number of shares issued services |
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|
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v3.25.0.1
SCHEDULE OF FINANCIAL ASSETS MEASURED AT FAIR VALUE ON A RECURRING BASIS (Details) - Fair Value, Recurring [Member] - USD ($) $ in Thousands |
Jan. 31, 2025 |
Jan. 31, 2024 |
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Total financial assets |
$ 17,114
|
$ 19,823
|
Money Market Funds [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Cash equivalents |
912
|
1,170
|
Exchange Traded Funds [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Short-term investments |
10
|
|
US Treasury Securities [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Short-term investments |
16,192
|
18,653
|
Fair Value, Inputs, Level 1 [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Total financial assets |
912
|
1,170
|
Fair Value, Inputs, Level 1 [Member] | Money Market Funds [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Cash equivalents |
912
|
1,170
|
Fair Value, Inputs, Level 1 [Member] | Exchange Traded Funds [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Short-term investments |
|
|
Fair Value, Inputs, Level 1 [Member] | US Treasury Securities [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Short-term investments |
|
|
Fair Value, Inputs, Level 2 [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Total financial assets |
16,202
|
18,653
|
Fair Value, Inputs, Level 2 [Member] | Money Market Funds [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Cash equivalents |
|
|
Fair Value, Inputs, Level 2 [Member] | Exchange Traded Funds [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Short-term investments |
10
|
|
Fair Value, Inputs, Level 2 [Member] | US Treasury Securities [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Short-term investments |
16,192
|
18,653
|
Fair Value, Inputs, Level 3 [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Total financial assets |
|
|
Fair Value, Inputs, Level 3 [Member] | Money Market Funds [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Cash equivalents |
|
|
Fair Value, Inputs, Level 3 [Member] | Exchange Traded Funds [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Short-term investments |
|
|
Fair Value, Inputs, Level 3 [Member] | US Treasury Securities [Member] |
|
|
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] |
|
|
Short-term investments |
|
|
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SCHEDULE OF SEGMENT INFORMATION (Details) - USD ($) $ in Thousands |
3 Months Ended |
|
Jan. 31, 2025 |
Jan. 31, 2024 |
Oct. 31, 2024 |
Segment Reporting Information [Line Items] |
|
|
|
Net income (loss) |
$ (3,213)
|
$ (3,290)
|
|
Total operating costs and expenses |
3,386
|
3,609
|
|
Less non-cash stock-based compensation |
(1,055)
|
(1,260)
|
|
Operating costs and expenses excluding non-cash share based compensation |
2,331
|
2,349
|
|
Total assets |
18,906
|
|
$ 21,591
|
Cancer Vaccines [Member] |
|
|
|
Segment Reporting Information [Line Items] |
|
|
|
Net income (loss) |
(2,018)
|
(1,756)
|
|
Operating costs and expenses excluding non-cash share based compensation |
1,467
|
1,213
|
|
Total assets |
11,863
|
|
12,917
|
CAR-T Therapeutics [Member] |
|
|
|
Segment Reporting Information [Line Items] |
|
|
|
Net income (loss) |
(1,177)
|
(1,525)
|
|
Operating costs and expenses excluding non-cash share based compensation |
848
|
1,128
|
|
Total assets |
6,885
|
|
8,535
|
Other [Member] |
|
|
|
Segment Reporting Information [Line Items] |
|
|
|
Net income (loss) |
(18)
|
(9)
|
|
Operating costs and expenses excluding non-cash share based compensation |
16
|
$ 8
|
|
Total assets |
$ 158
|
|
$ 139
|
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Anixa Biosciences (NASDAQ:ANIX)
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