Current Report Filing (8-k)
27 Septembre 2022 - 02:18PM
Edgar (US Regulatory)
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2022-09-27 iso4217:USD xbrli:shares iso4217:USD xbrli:shares
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM
8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported):
September 27, 2022
SYNTHETIC BIOLOGICS, INC.
(Exact name of registrant as specified in its charter)
Nevada |
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001-12584 |
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13-3808303 |
(State or other jurisdiction of
incorporation)
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(Commission File No.) |
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(IRS Employer Identification
No.)
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9605 Medical Center Drive,
Suite 270
Rockville,
Maryland
20850
(Address of principal executive offices and zip code)
(301)
417-4364
Registrant’s telephone number, including area code
N/A
(Former name or former address, if changed since last report)
Check the appropriate box below if the Form 8-K filing is intended
to simultaneously satisfy the filing obligation of the registrant
under any of the following provisions (see General Instruction A.2.
below):
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¨ |
Written communications pursuant to Rule 425 under
the Securities Act (17 CFR 230.425) |
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¨ |
Soliciting material pursuant to Rule 14a-12 under
the Exchange Act (17 CFR 240.14a-12) |
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Pre-commencement communications pursuant to Rule
14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
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Pre-commencement communications pursuant to Rule
13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
Title of each
class |
Trading Symbol(s) |
Name of each exchange on which
registered |
Common stock, par value $0.001 per share |
SYN |
NYSE American |
Indicate by check mark whether the registrant is an emerging growth
company as defined in in Rule 405 of the Securities Act of 1933 (17
CFR §230.405 of this chapter) or Rule 12b-2 of the Securities
Exchange Act of 1934 (17 CFR §240.12b-2 of this chapter).
Emerging growth company ¨
If an emerging growth company, indicate by checkmark 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. ¨
Item 7.01. Regulation FD
Disclosure.
On September 27, 2022, Synthetic Biologics, Inc. (the “Company”)
issued a press release announcing positive outcome from the Data
and Safety Monitoring Committee (“DSMC”) review of results from the
first Cohort of the Company’s Phase 1b/2a randomized,
double-blinded, placebo-controlled clinical trial of SYN-004
(ribaxamase) in allogeneic hematopoietic cell transplant (HCT)
recipients for the prevention of acute graft-versus-host-disease
(aGVHD).
The information in this Item 7.01 and in the press release
furnished as Exhibit 99.1 to this Current Report on Form 8-K shall
not be deemed to be “filed” for purposes of Section 18 of the
Securities Exchange Act of 1934, as amended, or otherwise subject
to the liabilities of that section or Sections 11 and 12(a)(2) of
the Securities Act of 1933, as amended and shall not be
incorporated by reference into any filing with the U.S. Securities
and Exchange Commission made by the Company, whether made before or
after the date hereof, regardless of any general incorporation
language in such filing.
The press release furnished as Exhibit 99.1 to this Current Report
on Form 8-K includes “safe harbor” language pursuant to the Private
Securities Litigation Reform Act of 1995, as amended, indicating
that certain statements contained therein are “forward-looking”
rather than historical.
Item 8.01. Other Events.
On September 27, 2022, the Company issued a press release
announcing positive outcome from the DSMC review of results from
the first Cohort of the Company’s Phase 1b/2a randomized,
double-blinded, placebo-controlled clinical trial of SYN-004
(ribaxamase) in allogeneic hematopoietic cell transplant (HCT)
recipients for the prevention of acute graft-versus-host-disease
(aGVHD).
Key data and conclusions disclosed in the press release
include:
Cohort 1 enrolled 19 patients who received at least 1 dose of study
drug (SYN-004 or Placebo randomized 2:1). Sixteen patients received
at least one dose of intravenous (IV) meropenem and 12 of these
patients completed sufficient doses of IV meropenem to be evaluable
towards the study endpoints. The study is on-going and remains
blinded; however, key findings from blinded data for Cohort 1 are
included below:
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· |
Adverse events (AEs)
and serious adverse events (SAEs) observed in Cohort 1 were typical
of those observed in allo-HCT patients and no AEs or SAEs were
determined to be related to study drug treatment by the
investigators. |
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o |
A total of 13 SAEs were reported
among 10 patients, with the most common SAE being infections and
infestations including sepsis. |
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o |
One patient died 14 days after the
last dose of study drug (within the 30-day reporting period) due to
sepsis that was not related to study drug. |
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· |
Consistent with
previous studies of SYN-004 in healthy volunteers, SYN-004 was not
observed in blood samples from the majority of the evaluable
patients. |
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o |
A
total of 3 plasma samples (~2% of all analyzed samples) had low but
quantifiable levels of SYN-004 using a sensitive ECL
assay. |
|
o |
None of the 3 ECL positive plasma
samples was found to contain active SYN-004 using a functional
enzyme activity assay. |
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· |
Meropenem
pharmacokinetics were as expected for this patient
population. |
Based on a review of the safety and pharmacokinetic data, the DSMC
has recommended that the study may proceed to enroll Cohort 2 in
which study drug (SYN-004 or Placebo) will be administered in
combination with the IV beta-lactam antibiotic
piperacillin/tazobactam.
Item 9.01. Financial Statements and Exhibits.
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of
1934, the registrant has duly caused this Current Report on Form
8-K to be signed on its behalf by the undersigned hereunto duly
authorized.
Dated: September 27,
2022 |
SYNTHETIC BIOLOGICS,
INC. |
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By: |
/s/ Steven A. Shallcross |
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Name: |
Steven A. Shallcross |
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Title: |
Chief Executive Officer and Chief Financial Officer
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Synthetic Biologics (AMEX:SYN)
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De Déc 2022 à Jan 2023
Synthetic Biologics (AMEX:SYN)
Graphique Historique de l'Action
De Jan 2022 à Jan 2023