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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

 

November 14, 2024

Date of Report (Date of earliest event reported)

 

MARKER THERAPEUTICS, INC.

(Exact name of registrant as specified in its charter)

 

Delaware 001-37939 45-4497941
(State or other jurisdiction of incorporation) (Commission File Number) (IRS Employer Identification No.)

 

2450 Holcombe Blvd, Suite BCM-A, MS: BCM251

Houston, Texas

  77021
(Address of principal executive offices)   (Zip Code)

 

(713400-6400

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 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))

 

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   MRKR   The Nasdaq Stock Market LLC

 

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).

 

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. ¨

 

 

 

 

 

 

Item 2.02 Results of Operations and Financial Condition.

 

On November 14, 2024, Marker Therapeutics, Inc. (the “Company”) reported financial results for the quarter ended September 30, 2024 and other recent corporate updates. A copy of the press release is furnished as Exhibit 99.1 to this report and incorporated by reference.

 

The information in this Item 2.02 of this Current Report on Form 8-K (including Exhibit 99.1) is furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or subject to the liabilities of that section or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended. The information shall not be deemed incorporated by reference into any other filing with the Securities and Exchange Commission made by the Company, whether made before or after today’s date, regardless of any general incorporation language in such filing, except as shall be expressly set forth by specific references in such filing.

 

Item 9.01.Financial Statements and Exhibits.

 

(d) Exhibits.

 

Exhibit No. Description 
   
99.1 Press Release dated November 14, 2024.
104 Cover Page Interactive Data File (embedded within the Inline XBRL document).

 

 

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

  Marker Therapeutics, Inc.
     
Dated: November 14, 2024 By: /s/ Juan Vera
    Juan Vera
    President and Chief Executive Officer

 

 

 

 

Exhibit 99.1 

 

 

 

Marker Therapeutics Reports Third Quarter 2024 Financial Results and Provides Business Updates

 

Marker Therapeutics to receive two grants from NIH Small Business Innovation Research (SBIR) program to support clinical investigation of MT-601 in patients with lymphoma and metastatic pancreatic cancer

 

Houston, TX — November 14, 2024 Marker Therapeutics, Inc. (Nasdaq: MRKR), a clinical-stage immuno-oncology company focusing on developing next-generation T cell-based immunotherapies for the treatment of hematological malignancies and solid tumors, today reported corporate updates and financial results for the third quarter ended September 30, 2024.

 

“As we approach the end of 2024, we continue to build momentum across our clinical and corporate programs,” said Juan Vera, M.D., President and Chief Executive Officer of Marker Therapeutics. “During the third quarter, we made significant progress in our ongoing Phase 1 APOLLO study investigating MT-601 in patients with lymphoma who have relapsed after anti-CD19 chimeric antigen receptor (CAR)-T cell therapy or where CAR-T cells are not an option. Enrollment is ongoing and we expect to be able to report preliminary safety and efficacy data by the end of this year. We, along with our study investigators, have been encouraged by the promising activity shown in this platform and look forward to continuing assessments from the trial.”

 

“We also recently strengthened our financial position with the receipt of two, $2 million Small Business Innovation Research (SBIR) grants from the National Institutes of Health (NIH). The non-dilutive funding will be used to support further development of MT-601 in patients with non-Hodgkin’s lymphoma who have relapsed following anti-CD19 CAR-T cell therapy, as well as assist in funding the clinical investigation of MT-601 in pancreatic cancer. We continue to make meaningful progress and remain focused on execution as we move our programs through the clinical trials,” added Dr. Vera.

 

PROGRAM UPDATES & EXPECTED MILESTONES

 

MT-601 (Lymphoma)

 

-Marker’s lead program is investigating MT-601 in the nationwide multicenter Phase 1 APOLLO study (clinicaltrials.gov identifier: NCT05798897) in patients with lymphoma who have relapsed after anti-CD19 CAR-T cell therapy or where CAR-T cells are not an option.

 

-The Company previously reported that one of the Principal Investigators presented preliminary safety and efficacy with sustained objective responses observed in three study participants treated at City of Hope National Medical Center (Press Release, April 8, 2024). Treatment was well tolerated among all study participants with no observation of severe adverse effects such as immune effector cell associated neurotoxicity syndrome (ICANS).

 

-All study participants continue to be observed for long-term treatment effects and durability of response.

 

 

 

 

 

 

-The Company is enrolling additional study participants in the Phase 1 APOLLO trial and expects to provide an update on safety and durability during the fourth quarter of 2024.

 

-Marker Therapeutics was awarded a $2 million grant from NIH Small Business Innovation Research Program (SBIR) to support the clinical investigation of MT-601 in patients with lymphoma who have relapsed following anti-CD19 CAR-T cell therapy (Press Release, August 12, 2024).

 

MT-601 (Pancreatic)

 

-The Company was awarded a $2 million grant from NIH Small Business Innovation Research (SBIR) Program to support the clinical investigation of MT-601 in patients with metastatic pancreatic cancer.

 

-The Company expects to start the clinical program of MT-601 in patients with metastatic pancreatic cancer in 2025.

 

MT-401-OTS (Acute Myeloid Leukemia or Myelodysplastic Syndrome)

 

-The Company previously secured non-dilutive funding to support the clinical investigation of MT-401-OTS in patients with Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS) and anticipates clinical program initiation during the first half of 2025.

 

THIRD QUARTER 2024 FINANCIAL HIGHLIGHTS

 

Cash Position and Guidance: At September 30, 2024, Marker had cash and cash equivalents of $9 million. The Company believes that its existing cash and cash equivalents will fund its operating expenses into October 2025. This estimate is subject to the Company’s ability to effectively manage its costs and utilize drawdowns of available grant funds.

 

R&D Expenses: Research and development expenses were $3.5 million for the quarter ended September 30, 2024, compared to $2.0 million for the quarter ended September 30, 2023 as a result of our increased clinical trial activity in the quarter.

 

G&A Expenses: General and administrative expenses were $0.9 million for the quarter ended September 30, 2024, compared to $1.4 million for the quarter ended September 30, 2023 reflecting the savings from the reorganization that was completed in late 2023.

 

Net Loss: Marker reported a net loss from continuing operations of $2.3 million for the quarter ended September 30, 2024, compared to $3.0 million for the quarter ended September 30, 2023.

 

About multiTAA-specific T cells

 

The multi-tumor associated antigen (multiTAA)-specific T cell platform is a novel, non-genetically modified cell therapy approach that selectively expands tumor-specific T cells from a patient's/donor’s blood capable of recognizing a broad range of tumor antigens. Unlike other T cell therapies, multiTAA-specific T cells allow the recognition of hundreds of different epitopes within up to six tumor-specific antigens, thereby reducing the possibility of tumor escape. Since multiTAA-specific T cells are not genetically engineered, Marker believes that its product candidates will be easier and less expensive to manufacture, with an improved safety profile, compared to current engineered T cell approaches, and may provide patients with meaningful clinical benefits.

 

 

 

 

 

About Marker Therapeutics, Inc.

 

Marker Therapeutics, Inc. is a Houston, TX-based clinical-stage immuno-oncology company specializing in the development of next-generation T cell-based immunotherapies for the treatment of hematological malignancies and solid tumors. Clinical trials that enrolled more than 200 patients across various hematological and solid tumor indications showed that the Company’s autologous and allogeneic multiTAA-specific T cell products were well tolerated and demonstrated durable clinical responses. Marker’s goal is to introduce novel T cell therapies to the market and improve patient outcomes. To achieve these objectives, the Company prioritizes the preservation of financial resources and focuses on operational excellence. Marker’s unique T cell platform is strengthened by non-dilutive funding from U.S. state and federal agencies supporting cancer research.

 

To receive future press releases via email, please visit: https://www.markertherapeutics.com/email-alerts.

 

Forward-Looking Statements

 

This release contains forward-looking statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Statements in this news release concerning the Company’s expectations, plans, business outlook or future performance, and any other statements concerning assumptions made or expectations as to any future events, conditions, performance or other matters, are “forward-looking statements.” Forward-looking statements include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things: our research, development and regulatory activities and expectations relating to our non-engineered multi-tumor antigen specific T cell therapies; the effectiveness of these programs or the possible range of application and potential curative effects and safety in the treatment of diseases; and the timing, conduct and success of our clinical trials of our product candidates, including MT-601 for the treatment of patients with lymphoma. Forward-looking statements are by their nature subject to risks, uncertainties and other factors which could cause actual results to differ materially from those stated in such statements. Such risks, uncertainties and factors include, but are not limited to the risks set forth in the Company’s most recent Form 10-K, 10-Q and other SEC filings which are available through EDGAR at WWW.SEC.GOV. The Company assumes no obligation to update its forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release except as may be required by law.

 

 

 

 

 

Marker Therapeutics, Inc.

Condensed Consolidated Balance Sheets

(Unaudited)

 

   September 30,   December 31, 
   2024   2023 
ASSETS          
Current assets:          
Cash and cash equivalents  $8,999,664   $15,111,450 
Prepaid expenses and deposits   1,166,274    988,126 
Other receivables   744,410    1,027,815 
Total current assets   10,910,348    17,127,391 
Total assets  $10,910,348   $17,127,391 
           
LIABILITIES AND STOCKHOLDERS’ EQUITY          
Current liabilities:          
Accounts payable and accrued liabilities  $2,557,335   $1,745,193 
Related party payable   903,438    1,329,655 
Total current liabilities   3,460,773    3,074,848 
Total liabilities   3,460,773    3,074,848 
           
Stockholders’ equity:          
Preferred stock, $0.001 par value, 5 million shares authorized, 0 shares issued and outstanding at September 30, 2024 and December 31, 2023, respectively        
Common stock, $0.001 par value, 30 million shares authorized, 8.9 million shares issued and outstanding as of September 30, 2024 and December 31, 2023 (see Note 9)   8,923    8,891 
Additional paid-in capital   450,620,206    450,329,515 
Accumulated deficit   (443,179,554)   (436,285,863)
Total stockholders’ equity   7,449,575    14,052,543 
Total liabilities and stockholders’ equity  $10,910,348   $17,127,391 

 

 

 

 

 

 

Marker Therapeutics, Inc.

Condensed Consolidated Statements of Operations

(Unaudited)

 

   For the Three Months Ended   For the Nine Months Ended 
   September 30,   September 30, 
   2024   2023   2024   2023 
Revenues:                
Grant income  $1,926,020   $257,606   $4,339,317   $2,254,601 
Total revenues   1,926,020    257,606    4,339,317    2,254,601 
Operating expenses:                    
Research and development   3,471,216    2,044,980    8,381,661    7,799,472 
General and administrative   854,677    1,412,672    3,214,611    6,098,716 
Total operating expenses   4,325,893    3,457,652    11,596,272    13,898,188 
Loss from operations   (2,399,873)   (3,200,046)   (7,256,955)   (11,643,587)
Other income (expenses):                    
Interest income   91,681    218,085    363,264    337,819 
Loss from continuing operations   (2,308,192)   (2,981,961)   (6,893,691)   (11,305,768)
Discontinued operations:                    
Loss from discontinued operations, net of tax               (2,922,406)
Gain on disposal of discontinued operations before income taxes               8,794,426 
Income from discontinued operations               5,872,020 
Net (loss) income  $(2,308,192)  $(2,981,961)  $(6,893,691)  $(5,433,748)
                     
Net (loss) earnings per share:                    
Loss from continuing operations, basic and diluted  $(0.26)  $(0.34)  $(0.77)  $(1.29)
Income from discontinued operations, basic  $   $   $   $0.67 
Income from discontinued operations, diluted  $   $   $   $0.66 
Net loss per share  $(0.26)  $(0.34)  $(0.77)  $(0.62)
                     
Weighted average number of common shares outstanding:                    
Basic   8,923,170    8,825,881    8,914,487    8,782,340 
Diluted   8,923,170    8,825,881    8,914,487    8,834,512 

 

 

 

 

 

Marker Therapeutics, Inc.

Condensed Consolidated Statements of Cash Flows

(Unaudited)

 

   For the Nine Months Ended 
   September 30, 
   2024   2023 
Cash Flows from Operating Activities:          
Net loss  $(6,893,691)  $(5,433,748)
Less: gain from discontinued operations, net of tax       5,872,020 
Net loss from continuing operations   (6,893,691)   (11,305,768)
Reconciliation of net loss to net cash used in operating activities:          
Stock-based compensation   195,320    714,899 
Changes in operating assets and liabilities:          
Prepaid expenses and deposits   (178,148)   (80,116)
Other receivables   283,405    2,318,691 
Related party payable   (426,217)   367,915 
Accounts payable and accrued expenses   812,142    (159,567)
Deferred revenue       107,530 
Net cash used in operating activities - continuing operations   (6,207,189)   (8,036,416)
Net cash used in operating activities - discontinued operations       (6,035,961)
Net cash used in operating activities   (6,207,189)   (14,072,377)
Cash Flows from Investing Activities:          
Net cash provided by investing activities - discontinued operations       18,664,122 
Net cash provided by investing activities       18,664,122 
Cash Flows from Financing Activities:          
Proceeds from issuance of common stock, net   36,902    1,014,640 
Proceeds from stock options exercise   58,501    85,342 
Net cash provided by financing activities   95,403    1,099,982 
Net (decrease) increase in cash and cash equivalents   (6,111,786)   5,691,727 
Cash and cash equivalents at beginning of the period   15,111,450    11,782,172 
Cash and cash equivalents at end of the period  $8,999,664   $17,473,899 

 

Contacts

Investors

TIBEREND STRATEGIC ADVISORS, INC.

Jonathan Nugent

205-566-3026

jnugent@tiberend.com

 

 

 

 

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