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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) |
(713) 400-6400
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.
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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