0001557746false00015577462024-08-072024-08-07

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

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FORM 8-K

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CURRENT REPORT

Pursuant to Section 13 or 15(d) of

The Securities Exchange Act of 1934

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Date of Report (Date of earliest event reported): August 7, 2024

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Aclaris Therapeutics, Inc.

(Exact name of registrant as specified in its charter)

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Delaware

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001-37581

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46-0571712

(State or other jurisdiction of incorporation)

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(Commission File Number)

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(IRS Employer
Identification No.)

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701 Lee Road, Suite 103

Wayne, PA 19087

(Address of principal executive offices, including zip code)

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(484) 324-7933

(Registrant’s telephone number, including area code)

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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:

☐ Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

☐ Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

☐ Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

☐ Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

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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, $0.00001 par value

 

ACRS

 

The Nasdaq Stock Market, LLC

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Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

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Emerging growth company ☐

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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. ☐

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Item 2.02 Results of Operations and Financial Condition.

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On August 7, 2024, Aclaris Therapeutics, Inc. (the “Registrant”) issued a press release announcing its financial results for the quarter and six months ended June 30, 2024. A copy of this press release is furnished herewith as Exhibit 99.1 to this Current Report.

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In accordance with General Instruction B.2. of Form 8-K, the information in this Item 2.02 and Exhibit 99.1 hereto shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liability of that section, nor shall it be deemed incorporated by reference in any of the Registrant’s filings under the Securities Act of 1933, as amended (the “Securities Act”), or the Exchange Act, whether made before or after the date hereof, regardless of any incorporation language in such a filing, except as expressly set forth by specific reference in such a filing.

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Item 9.01 Financial Statements and Exhibits.

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(d) Exhibits

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Exhibit

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Number

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Exhibit Description

99.1

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Press Release, dated August 7, 2024.

104

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The cover page from Aclaris Therapeutics, Inc.’s Form 8-K filed on August 7, 2024, formatted in Inline XBRL.

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2

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SIGNATURES

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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 hereunto duly authorized.

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ACLARIS THERAPEUTICS, INC.

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​

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Date: August 7, 2024

By:  

/s/ Kevin Balthaser

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Kevin Balthaser
Chief Financial Officer

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3

Exhibit 99.1

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Aclaris Therapeutics Reports Second Quarter 2024 Financial Results and Provides a Corporate Update

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-Initiated Phase 2a Study Activities for ATI-2138 in Atopic Dermatitis-

-Strengthened Balance Sheet Through Sale of Future OLUMIANT® Royalties for Proceeds of up to $31.5 Million-

​

WAYNE, Pa., Aug. 07, 2024 (GLOBE NEWSWIRE) -- Aclaris Therapeutics, Inc. (NASDAQ: ACRS), a clinical-stage biopharmaceutical company focused on developing novel drug candidates for immuno-inflammatory diseases, today announced its financial results for the second quarter of 2024 and provided a corporate update.

“With study activities underway for our ATI-2138 Phase 2a trial in moderate to severe atopic dermatitis and the strengthening of our balance sheet through the completion of our royalty purchase agreement with OMERS, we're well-positioned to drive our strategic initiatives forward,” said Dr. Neal Walker, Interim President & CEO and Chair of the Board of Directors of Aclaris. “Our focus remains on leveraging our resources to maximize the potential of our innovative drug candidates, pursue available opportunities, and create long-term value for patients and shareholders alike.”

Research and Development Highlights:

·ITK Inhibitor Programs

oATI-2138, an investigational oral covalent ITK/JAK3 inhibitor
◾ATI-2138-AD-201: Aclaris is activating clinical sites and expects to enroll patients in the coming weeks in this Phase 2a open-label trial to investigate the safety, tolerability, pharmacokinetics, efficacy, and pharmacodynamics of ATI-2138 in subjects with moderate to severe atopic dermatitis (AD).
oITK Selective Compound
◾Aclaris is progressing to development candidate selection a second generation ITK selective inhibitor for autoimmune indications.

·

Lepzacitinib (ATI-1777), an investigational topical “soft” JAK 1/3 inhibitor

oIn January 2024, Aclaris reported positive top-line results from its Phase 2b trial of lepzacitinib in atopic dermatitis (AD).
oAclaris is currently seeking a global development and commercialization partner for this program (excluding Greater China). As previously announced, in 2022 Aclaris granted Pediatrix Therapeutics exclusive rights to develop and commercialize lepzacitinib in Greater China.

·

Zunsemetinib (ATI-450), an investigational oral small molecule MK2 inhibitor

oAclaris plans to support Washington University in St. Louis in its investigator-initiated Phase 1b/2 trials of zunsemetinib as a potential treatment for pancreatic cancer and metastatic breast cancer. Aclaris expects these trials to be primarily funded by grants awarded to Washington University.

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Financial Highlights:

Liquidity and Capital Resources

As of June 30, 2024, Aclaris had aggregate cash, cash equivalents and marketable securities of $149.9 million compared to $181.9 million as of December 31, 2023. In July 2024, Aclaris received an upfront payment of $26.5 million and is eligible to receive up to an additional $5.0 million upon the achievement of certain sales milestones in connection with the sale of OLUMIANT® royalties and milestones to OMERS Life Sciences.

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Aclaris anticipates that its cash, cash equivalents and marketable securities as of June 30, 2024 in combination with the $26.5 million from the sale of OLUMIANT® royalties and milestones will be sufficient to fund its operations into 2028, without giving effect to any potential new business development transactions, additional financing activities or the outcome of its strategic review.

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Financial Results

Second Quarter 2024

●Net loss was $11.0 million for the second quarter of 2024 compared to $29.6 million for the second quarter of 2023.
●Total revenue was $2.8 million for the second quarter of 2024 compared to $1.9 million for the second quarter of 2023. The increase was primarily driven by an increase in royalties under the Lilly license agreement during the three months ended June 30, 2024.
●Research and development (R&D) expenses were $8.8 million for the quarter ended June 30, 2024 compared to $25.3 million for the prior year period.
oThe $16.5 million decrease was primarily the result of lower:
◾Zunsemetinib development expenses associated with clinical activities for a Phase 2a trial for hidradenitis suppurativa which was completed in March 2023, a Phase 2b trial for rheumatoid arthritis which was completed in November 2023, a Phase 2b trial for psoriatic arthritis which was discontinued in December 2023, and drug candidate manufacturing costs;
◾Costs associated with lepzacitinib preclinical development activities and a Phase 2b clinical trial for AD which was completed in January 2024;
◾ATI-2138 development expenses, including costs associated with a Phase 1 MAD trial which was completed in September 2023 and other preclinical activities; and
◾Compensation-related expenses due to a decrease in headcount and higher forfeiture credits.
●General and administrative (G&A) expenses were $4.8 million for the quarter ended June 30, 2024 compared to $8.3 million for the prior year period. The decrease was primarily due to a reduction in compensation-related expenses due to lower headcount and higher forfeiture credits, along with the recognition of bad debt expense recorded in the prior year period from Aclaris’ determination that collection of amounts due from EPI Health are uncertain as a result of their filing for Chapter 11 bankruptcy protection.
●Licensing expenses were $1.3 million for the quarter ended June 30, 2024 compared to $0.6 million for the prior year period. The increase was due to an increase in royalties earned under the Lilly license agreement.
●Revaluation of contingent consideration resulted in a $0.2 million loss for the quarter ended June 30, 2024 compared to a gain of $1.5 million for the prior year period.

Year-to-date 2024

●Net loss was $27.9 million for the six months ended June 30, 2024 compared to $57.7 million for the six months ended June 30, 2023.
●Total revenue was $5.2 million for the six months ended June 30, 2024 compared to $4.4 million for the six months ended June 30, 2023. The increase was primarily driven by an increase in royalties under the Lilly license agreement during the six months ended June 30, 2024.
●R&D expenses were $18.6 million for the six months ended June 30, 2024 compared to $47.9 million for the prior year period.
oThe $29.3 million decrease was primarily the result of lower:
◾Zunsemetinib development expenses associated with clinical activities for a Phase 2a trial for hidradenitis suppurativa which was completed in March 2023, a Phase 2b trial for rheumatoid arthritis which was completed in November 2023, a Phase 2b trial for psoriatic arthritis which was discontinued in December 2023, and drug candidate manufacturing costs;
◾Costs associated with lepzacitinib preclinical development activities and a Phase 2b clinical trial for AD which was completed in January 2024;
◾ATI-2138 development expenses, including costs associated with a Phase 1 MAD trial which was completed in September 2023 and other preclinical activities; and
◾Compensation-related expenses due to a decrease in headcount and higher forfeiture credits.
●G&A expenses were $11.6 million for the six months ended June 30, 2024 compared to $17.1 million for the prior year period. The decrease was primarily due to a reduction in compensation-related expenses due to lower headcount and higher forfeiture credits, a decrease in patent, legal and accounting related expenses, and the recognition of bad debt expense recorded in the prior year period from Aclaris’ determination that collection of amounts due from EPI Health are uncertain as a result of their filing for Chapter 11 bankruptcy protection.
●Licensing expenses were $2.3 million for the six months ended June 30, 2024 compared to $1.6 million for the prior year period. The increase was due to an increase in royalties earned under the Lilly license agreement.
●Revaluation of contingent consideration resulted in a $3.0 million loss for the six months ended June 30, 2024 compared to a gain of $2.3 million for the prior year period.

OLUMIANT® is a registered trademark of Eli Lilly and Company.

​

About Aclaris Therapeutics, Inc.

Aclaris Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing a pipeline of novel drug candidates to address the needs of patients with immuno-inflammatory diseases who lack satisfactory treatment options. The company has a multi-stage portfolio of drug candidates powered by a robust R&D engine exploring protein kinase regulation. For additional information, please visit www.aclaristx.com.

Cautionary Note Regarding Forward-Looking Statements

Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. These statements may be identified by words such as “anticipate,” “believe,” “expect,” “intend,” “may,” “plan,” “potential,” “will,” and similar expressions, and are based on Aclaris’ current beliefs and expectations. These forward-looking statements include expectations regarding its plans for its development programs, including its plans to seek a development and commercialization partner for lepzacitinib, the clinical development of ATI-2138, its plan to support Washington University in St. Louis in its investigator-initiated Phase 1b/2 trials of zunsemetinib, the sufficiency of its cash, cash equivalents and marketable securities to fund its operations into 2028, as well as its strategic plans and strategic review. These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements. Risks and uncertainties that may cause actual results to differ materially include uncertainties inherent in the conduct of clinical trials, Aclaris’ reliance on third parties over which it may not always have full control, Aclaris’ ability to enter into strategic partnerships on commercially reasonable terms, the uncertainty regarding the macroeconomic environment and other risks and uncertainties that are described in the Risk Factors section of Aclaris’ Annual Report on Form 10-K for the year ended December 31, 2023, and other filings Aclaris makes with the U.S. Securities and Exchange Commission from time to time. These documents are available under the “SEC Filings” page of the “Investors” section of Aclaris’ website at www.aclaristx.com. Any forward-looking statements speak only as of the date of this press release and are based on information available to Aclaris as of the date of this release, and Aclaris assumes no obligation to, and does not intend to, update any forward-looking statements, whether as a result of new information, future events or otherwise.

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Aclaris Therapeutics, Inc.

Condensed Consolidated Statements of Operations

(unaudited, in thousands, except share and per share data)

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​

​

​

​

​

​

​

​

​

​

​

​

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Three Months Ended

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Six Months Ended

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​

June 30,

​

June 30,

​

    

2024

    

2023

    

2024

    

2023

Revenues:

​

​

​

​

​

​

​

​

​

​

​

​

Contract research

​

$

625

​

$

875

​

$

1,281

​

$

1,764

Licensing

​

​

2,141

​

​

994

​

​

3,882

​

​

2,633

Total revenue

​

​

2,766

​

​

1,869

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​

5,163

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​

4,397

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​

​

​

​

​

​

​

​

​

​

​

​

Costs and expenses:

​

​

​

​

​

​

​

​

​

​

​

​

Cost of revenue (1)

​

​

624

​

​

1,042

​

​

1,433

​

​

1,850

Research and development (1)

​

​

8,759

​

​

25,275

​

​

18,604

​

​

47,862

General and administrative (1)

​

​

4,752

​

​

8,317

​

​

11,596

​

​

17,107

Licensing

​

​

1,285

​

​

550

​

​

2,316

​

​

1,611

Revaluation of contingent consideration

​

​

200

​

​

(1,500)

​

​

3,000

​

​

(2,300)

Total costs and expenses

​

​

15,620

​

​

33,684

​

​

36,949

​

​

66,130

Loss from operations

​

​

(12,854)

​

​

(31,815)

​

​

(31,786)

​

​

(61,733)

Other income, net

​

​

1,868

​

​

2,246

​

​

3,859

​

​

4,004

Net loss

​

$

(10,986)

​

$

(29,569)

​

$

(27,927)

​

$

(57,729)

Net loss per share, basic and diluted

​

$

(0.15)

​

$

(0.42)

​

$

(0.39)

​

$

(0.84)

Weighted average common shares outstanding, basic and diluted

​

​

71,291,400

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​

70,633,528

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​

71,183,129

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​

68,763,542

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(1) Amounts include stock-based compensation expense as follows:

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​

​

​

​

​

​

​

​

​

​

​

​

Cost of revenue

​

$

223

​

$

473

​

$

475

​

$

772

Research and development

​

​

1,097

​

​

3,494

​

​

1,068

​

​

6,096

General and administrative

​

​

1,583

​

​

2,555

​

​

3,449

​

​

6,460

Total stock-based compensation expense

​

$

2,903

​

$

6,522

​

$

4,992

​

$

13,328

​

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Aclaris Therapeutics, Inc.

Selected Consolidated Balance Sheet Data

(unaudited, in thousands, except share data)

​

    

June 30, 2024

    

December 31, 2023

Cash, cash equivalents and marketable securities

​

$

149,871

​

$

181,877

Total assets

​

$

161,071

​

$

197,405

Total current liabilities

​

$

15,682

​

$

30,952

Total liabilities

​

$

27,249

​

$

40,226

Total stockholders’ equity

​

$

133,822

​

$

157,179

Common stock outstanding

​

​

71,332,825

​

​

70,894,889

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Aclaris Therapeutics, Inc.

Selected Consolidated Cash Flow Data

(unaudited, in thousands)

​

​

Six Months Ended

​

Six Months Ended

​

​

June 30, 2024

​

June 30, 2023

Net loss

​

$

(27,927)

​

$

(57,729)

Depreciation and amortization

​

​

485

​

​

416

Stock-based compensation expense

​

​

4,992

​

​

13,328

Revaluation of contingent consideration

​

​

3,000

​

​

(2,300)

Changes in operating assets and liabilities

​

​

(13,687)

​

​

(722)

Net cash used in operating activities

​

$

(33,137)

​

$

(47,007)

​

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Aclaris Therapeutics Contact:

investors@aclaristx.com

​

Graphic

v3.24.2.u1
Document and Entity Information
Aug. 07, 2024
Document and Entity Information  
Document Type 8-K
Document Period End Date Aug. 07, 2024
Entity File Number 001-37581
Entity Registrant Name Aclaris Therapeutics, Inc.
Entity Incorporation, State or Country Code DE
Entity Tax Identification Number 46-0571712
Entity Address, Address Line One 701 Lee Road
Entity Address, Adress Line Two Suite 103
Entity Address, City or Town Wayne
Entity Address, State or Province PA
Entity Address, Postal Zip Code 19087
City Area Code 484
Local Phone Number 324-7933
Written Communications false
Soliciting Material false
Pre-commencement Tender Offer false
Pre-commencement Issuer Tender Offer false
Title of 12(b) Security Common Stock, $0.00001 par value
Trading Symbol ACRS
Security Exchange Name NASDAQ
Entity Emerging Growth Company false
Entity Central Index Key 0001557746
Amendment Flag false
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