Full Press Release Details
Marker Therapeutics Reports Third Quarter 2023
Financial Results and Provides Business Updates
Announced complete response in first patient
with lymphoma treated with MT-601 in Phase 1 APOLLO trial following CAR T relapse
Received Orphan Drug Designation (ODD) from
European Medicines Agency (EMA) for multiTAA-specific T cell product candidate MT-401 (zedenoleucel) for the treatment of patients with
Acute Myeloid Leukemia (AML)
Demonstrated enhanced anti-tumor activity in
an aggressive, treatment-resistant AML cell line and provided an update on clinical readiness of the MT-401 Off-the-Shelf (OTS) program
HOUSTON, November 9, 2023 (GLOBE NEWSWIRE)
-- 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 tumor indications, today reported corporate updates and financial
results for the third quarter ended September 30, 2023.
"During the third quarter of 2023, we continued
to diligently advance and execute our clinical objectives across our novel multiTAA-specific T cell pipeline," commented Juan F.
Vera, M.D., President and Chief Executive Officer of Marker Therapeutics. "Among the many highlights, we announced in September
that we observed a complete response in the first patient with lymphoma treated with MT-601, our multiTAA-specific T cell product candidate
targeting six antigens. This study participant was enrolled in our Phase 1 APOLLO trial after failing anti-CD19 CAR T cell therapy. The
positive clinical outcome in this CAR T relapsed participant is supported by non-clinical proof-of-concept data and highlights the potential
of MT-601 in patients who have relapsed after CAR T cell therapy. Together with the favorable clinical safety and tolerability profile,
MT-601 may represent a suitable alternative for the treatment of patients with lymphoma."
"In July, our MT-401 program was granted
Orphan Drug Designation by the EMA for the treatment of patients with AML," continued Dr. Vera. "We also reported non-clinical
proof-of-concept data from our MT-401-OTS program, which indicated the potential anti-tumor activity of the product in a partially human
leukocyte antigen (HLA) matched setting. With the clearance of our clinical protocol for MT 401 OTS from the U.S. FDA and the
added validation from our non-clinical work, we anticipate initiating a clinical trial in 2024 to evaluate the potential of this novel
therapy in patients with relapsed/refractory AML."
"To maximize shareholder value and
accelerate our patient-centric mission, we continue to engage in internal and external conversations with pertinent stakeholders to
optimize our clinical development plan, which we expect to announce in the first quarter of 2024. With our healthy balance sheet and
clinical progress shown to date, we believe we are well poised to achieve our near-and long-term growth objectives," concluded
Program Updates and Expected Milestones:
MT-401 (Acute Myeloid Leukemia)
Third Quarter 2023 Financial Highlights:
About Marker Therapeutics, Inc.
Marker Therapeutics, Inc. is a clinical-stage
immuno-oncology company specializing in the development of next-generation T cell-based immunotherapies for the treatment of hematological
malignancies and solid tumor indications. The T cell therapy technology developed by Marker is based on the selective expansion of non-engineered,
tumor-specific T cells that recognize tumor associated antigens (i.e., tumor targets) and kill tumor cells expressing those targets. This
population of T cells is designed to attack multiple tumor targets following infusion into patients and to activate the patient's
immune system to produce broad spectrum anti-tumor activity. Because Marker does not genetically engineer the T cells, Marker believes
that its product candidates will be easier and less expensive to manufacture, with reduced toxicities, compared to current engineered
CAR T and TCR-based approaches, and may provide patients with meaningful clinical benefit. As a result, Marker believes its portfolio
of T cell therapies has a compelling product profile, as compared to current gene-modified CAR T and TCR-based therapies.
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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 Marker'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; the timing,
conduct and success of our clinical trials of our product candidates, including MT-601 for the treatment of patients with lymphoma
and MT-401 for the treatment of patients with AML; the potential benefits of orphan drug designation to MT401; and our future
operating expenses and capital expenditure requirements, including our anticipated cash runway. 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
Marker's most recent Form 10-K, 10-Q and other SEC filings which are available through EDGAR at WWW.SEC.GOV. Marker 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
| September 30, | December 31, | |||||||
| 2023 | 2022 | |||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 17,473,899 | $ | 11,782,172 | ||||
| Prepaid expenses and deposits | 1,929,355 | 1,849,239 | ||||||
| Other receivables | 83,313 | 2,402,004 | ||||||
| Current assets of discontinued operations | - | 585,840 | ||||||
| Total current assets | 19,486,567 | 16,619,255 | ||||||
| Non-current assets of discontinued operations | - | 17,802,929 | ||||||
| Total assets | $ | 19,486,567 | $ | 34,422,184 | ||||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
| Current liabilities: | ||||||||
| Accounts payable and accrued liabilities | $ | 2,304,019 | $ | 2,521,193 | ||||
| Related party payable | 367,915 | - | ||||||
| Deferred revenue | 107,530 | - | ||||||
| Current liabilities of discontinued operations | - | 5,260,616 | ||||||
| Total current liabilities | 2,779,464 | 7,781,809 | ||||||
| Non-current liabilities of discontinued operations | - | 7,039,338 | ||||||
| Total liabilities | 2,779,464 | 14,821,147 | ||||||
| Stockholders' equity: | ||||||||
| Preferred stock, $0.001 par value, 5 million shares authorized, 0 shares issued and outstanding at September 30, 2023 and December 31, 2022, respectively | - | - | ||||||
| Common stock, $0.001 par value, 30 million shares authorized, 8.8 million and 8.4 million shares issued and outstanding as of September 30, 2023 and December 31, 2022, respectively | 8,888 | 8,406 | ||||||
| Additional paid-in capital | 450,181,012 | 447,641,680 | ||||||
| Accumulated deficit | (433,482,797 | ) | (428,049,049 | ) | ||||
| Total stockholders' equity | 16,707,103 | 19,601,037 | ||||||
| Total liabilities and stockholders' equity | $ | 19,486,567 | $ | 34,422,184 |
Marker Therapeutics, Inc.
Condensed Consolidated Statements of Operations
| For the Three Months Ended | For the Nine Months Ended | |||||||||||||||
| September 30, | September 30, | |||||||||||||||
| 2023 | 2022 | 2023 | 2022 | |||||||||||||
| Revenues: | ||||||||||||||||
| Grant income | $ | 257,606 | $ | 999,571 | $ | 2,254,601 | $ | 2,754,401 | ||||||||
| Total revenues | 257,606 | 999,571 | 2,254,601 | 2,754,401 | ||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | 2,044,980 | 3,591,897 | 7,799,472 | 9,786,138 | ||||||||||||
| General and administrative | 1,412,672 | 3,234,133 | 6,098,716 | 9,720,598 | ||||||||||||
| Total operating expenses | 3,457,652 | 6,826,030 | 13,898,188 | 19,506,736 | ||||||||||||
| Loss from operations | (3,200,046 | ) | (5,826,459 | ) | (11,643,587 | ) | (16,752,335 | ) | ||||||||
| Other income (expenses): | ||||||||||||||||
| Arbitration settlement | - | - | - | (118,880 | ) | |||||||||||
| Interest income | 218,085 | 99,750 | 337,819 | 138,653 | ||||||||||||
| Loss from continuing operations | (2,981,961 | ) | (5,726,709 | ) | (11,305,768 | ) | (16,732,562 | ) | ||||||||
| Discontinued operations: | ||||||||||||||||
| Loss from discontinued operations, net of tax | - | (1,192,874 | ) | (2,922,406 | ) | (9,341,717 | ) | |||||||||
| Gain on disposal of discontinued operations | - | - | 8,794,426 | - | ||||||||||||
| Income (loss) from discontinued operations | - | (1,192,874 | ) | 5,872,020 | (9,341,717 | ) | ||||||||||
| Net loss | $ | (2,981,961 | ) | $ | (6,919,583 | ) | $ | (5,433,748 | ) | $ | (26,074,279 | ) | ||||
| Net earnings (loss) per share: | ||||||||||||||||
| Loss from continuing operations, basic and diluted | $ | (0.34 | ) | $ | (0.69 | ) | $ | (1.29 | ) | $ | (2.01 | ) | ||||
| Income (loss) from discontinued operations, basic | $ | - | $ | (0.14 | ) | $ | 0.67 | $ | (1.12 | ) | ||||||
| Income (loss) from discontinued operations, diluted | $ | - | $ | (0.14 | ) | $ | 0.66 | $ | (1.12 | ) | ||||||
| Net loss per share | $ | (0.34 | ) | $ | (0.83 | ) | $ | (0.62 | ) | $ | (3.13 | ) | ||||
| Weighted average number of common shares outstanding: | ||||||||||||||||
| Basic | 8,825,881 | 8,359,920 | 8,782,340 | 8,343,477 | ||||||||||||
| Diluted | 8,825,881 | 8,359,920 | 8,834,512 | 8,343,477 |
Marker Therapeutics, Inc.
Condensed Consolidated Statements of Cash Flows
| For the Nine Months Ended | ||||||||
| September 30, 2023 | ||||||||
| 2023 | 2022 | |||||||
| Cash Flows from Operating Activities: | ||||||||
| Net loss | $ | (5,433,748 | ) | $ | (26,074,279 | ) | ||
| Less: gain (loss) from discontinued operations, net of tax | 5,872,020 | (9,341,717 | ) | |||||
| Net loss from continuing operations | (11,305,768 | ) | (16,732,562 | ) | ||||
| Reconciliation of net loss to net cash used in operating activities: | ||||||||
| Stock-based compensation | 714,899 | 2,921,765 | ||||||
| Gain on lease termination | - | (278,681 | ) | |||||
| Changes in operating assets and liabilities: | ||||||||
| Prepaid expenses and deposits | (80,116 | ) | (204,222 | ) | ||||
| Other receivables | 2,318,691 | (1,680,782 | ) | |||||
| Accounts payable and accrued expenses | 208,348 | (289,148 | ) | |||||
| Deferred revenue | 107,530 | (1,146,186 | ) | |||||
| Net cash used in operating activities - continuing operations | (8,036,416 | ) | (17,409,816 | ) | ||||
| Net cash used in operating activities - discontinued operations | (6,035,961 | ) | (3,256,915 | ) | ||||
| Net cash used in operating activities | (14,072,377 | ) | (20,666,731 | ) | ||||
| Cash Flows from Investing Activities: | ||||||||
| Net cash provided by (used in) investing activities - discontinued operations | 18,664,122 | (4,817,794 | ) | |||||
| Net cash provided by (used in) investing activities | 18,664,122 | (4,817,794 | ) | |||||
| Cash Flows from Financing Activities: | ||||||||
| Proceeds from issuance of common stock, net | 1,014,640 | 63,573 | ||||||
| Proceeds from stock options exercise | 85,342 | - | ||||||
| Net cash provided by financing activities | 1,099,982 | 63,573 | ||||||
| Net increase (decrease) in cash, cash equivalents and restricted cash | 5,691,727 | (25,420,952 | ) | |||||
| Cash, cash equivalents and restricted cash at beginning of the period | 11,782,172 | 43,497,331 | ||||||
| Cash, cash equivalents and restricted cash at end of the period | $ | 17,473,899 | $ | 18,076,379 |
TIBEREND STRATEGIC ADVISORS, INC.
Daniel Kontoh-Boateng