MRKR Marker Therapeutics Inc

Marker Therapeutics, Inc. (Nasdaq: MRKR), 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, today provided a corporate update and reported financial results for the third quarter ended September 30, 2022.

“This quarter we reached a major milestone in treating the first six patients in our Phase 2 AML trial with T cells derived from our new manufacturing process, which are designed for increased potency against tumor antigens,” said Peter L. Hoang, Marker’s President and Chief Executive Officer. “We are also pleased to receive a grant from the FDA Orphan Products program to support the Phase 2 treatment arm evaluating MT-401 in patients with minimal residual disease. We believe the MRD-positive patient population represents a significant opportunity for MT-401 as we continue to dose more patients in the trial and measure long-term response.”

PROGRAM UPDATES AND EXPECTED MILESTONES

Acute Myeloid Leukemia (MT-401)

• In September 2022, Marker announced that it had been awarded a $2 million grant from the U.S. Food and Drug Administration (FDA) Orphan Products Grants program to support the Phase 2 ARTEMIS trial of the company’s lead multi-tumor-associated antigen (MultiTAA) T cell product candidate, MT-401, in patients with post-transplant AML. The FDA grant will support the Company’s treatment arm evaluating MT-401 in patients with post-transplant AML with minimal residual disease. MT-401 was granted Orphan Drug Designation for the treatment of patients with AML following allogeneic stem cell transplant in 2020.
• The Company has treated all six patients in Cohorts 4 and 5 using MT-401 manufactured with Marker’s new T cell manufacturing process. The new manufacturing process is designed to produce a more potent product with increased antigen specificity and diversity and a reduction in manufacturing time. To date, all six patients have completed dose-limiting toxicity (DLT) periods with no DLTs reported. The Company expects to announce an efficacy analysis from the six patients in Cohorts 4 and 5 by year-end.
• Marker remains on track to dose the first patient in 2023 with MT-401-OTS, a scalable, off-the-shelf product candidate with the potential to match patients to treatment in under three days. The Company is in the process of developing a patient cell bank inventory.

Lymphoma (MT-601)

• In August 2022, Marker announced that the U.S. FDA cleared the Company’s Investigational New Drug Application (IND) for a Phase 1 study of MT-601, a multiTAA-specific T cell product targeting six antigens, for the treatment of patients with relapsed/refractory non-Hodgkin lymphoma who have failed or are ineligible to receive anti-CD19 CAR T cell treatment.
• The Company expects some sites to open before the end of the year and to enroll the first patient in the Phase 1 trial in Q1 of 2023.

Pancreatic Cancer (MT-601)

• The Company intends to initiate a Phase 1 multicenter study of MT-601 administered in combination with front-line chemotherapy to patients with locally advanced unresectable or metastatic pancreatic cancer in 2023.

THIRD QUARTER 2022 FINANCIAL RESULTS

• Cash Position and Guidance: At September 30, 2022, Marker had cash and cash equivalents of $18.1 million.
• Revenues: For the quarter ended September 30, 2022, Marker recorded $1.0 million of grant income and $2.95 million of related party service revenue.
• R&D Expenses: Research and development expenses were $7.3 million for the quarter ended September 30, 2022, compared to $6.8 million for the quarter ended September 30, 2021.
• G&A Expenses: General and administrative expenses were $3.7 million for the quarter ended September 30, 2022, compared to $3.2 million for the quarter ended September 30, 2021.
• Net Loss: Marker reported a net loss of $6.9 million for the quarter ended September 30, 2022, compared to a net loss of $12.4 million for the quarter ended September 30, 2021. 

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. Marker’s cell therapy technology 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 its T cell therapies, we believe that our 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 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; the timing, conduct and success of our clinical trials of our product candidates; our ability to use our manufacturing facilities to support clinical and commercial demand; and our future operating expenses and capital expenditure requirements. 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. Such risks and uncertainties may be amplified by the COVID-19 pandemic and its impact on our business and the global economy. The Company assumes no obligation to update our forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release.

Marker Therapeutics, Inc.Condensed Consolidated Balance Sheets(Unaudited)

	September 30,				December 31,
		2022				2021
ASSETS
Current assets:
Cash and cash equivalents	$	18,076,379			$	42,351,145
Restricted cash		-				1,146,186
Prepaid expenses and deposits		2,665,668				2,484,634
Other receivables		1,681,019				237
Total current assets		22,423,066				45,982,202
Non-current assets:
Property, plant and equipment, net		13,059,816				10,096,861
Construction in progress		-				2,225,610
Right-of-use assets, net		5,631,683				9,830,461
Total non-current assets		18,691,499				22,152,932
Total assets	$	41,114,565			$	68,135,134
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable and accrued liabilities	$	5,746,404			$	11,134,913
Related party deferred revenue		5,050,000				-
Lease liability		490,449				620,490
Deferred revenue		-				1,146,186
Total current liabilities		11,286,853				12,901,589
Non-current liabilities:
Lease liability, net of current portion		7,225,990				11,247,950
Total non-current liabilities		7,225,990				11,247,950
Total liabilities		18,512,843				24,149,539
Stockholders' equity:
Preferred stock - $0.001 par value, 5 million shares authorized and 0 shares issued and outstanding at September 30, 2022 and December 31, 2021, respectively		-				-
Common stock, $0.001 par value, 300 million and 150 million shares authorized, 83.6 million and 83.1 million shares issued and outstanding as of September 30, 2022 and December 31, 2021, respectively		83,599				83,079
Additional paid-in capital		446,710,757				442,020,871
Accumulated deficit		(424,192,634	)			(398,118,355	)
Total stockholders' equity		22,601,722				43,985,595
Total liabilities and stockholders' equity	$	41,114,565			$	68,135,134

Marker Therapeutics, Inc.Condensed Consolidated Statements of Operations(Unaudited)

	For the Three Months Ended								For the Nine Months Ended
	September 30,								September 30,
		2022				2021				2022				2021
Revenues:
Grant income	$	999,571			$	-			$	2,754,401			$	-
Related partry service revenue		2,950,000				-				2,950,000				-
Total revenues		3,949,571				-				5,704,401				-
Operating expenses:
Research and development		7,290,899				6,784,390				20,872,264				19,777,454
General and administrative		3,678,005				3,239,148				10,926,189				9,936,256
Total operating expenses		10,968,904				10,023,538				31,798,453				29,713,710
Loss from operations		(7,019,333	)			(10,023,538	)			(26,094,052	)			(29,713,710	)
Other income (expenses):
Arbitration settlement		-				(2,406,576	)			(118,880	)			(2,406,576	)
Interest income		99,750				791				138,653				4,731
Net loss	$	(6,919,583	)		$	(12,429,323	)		$	(26,074,279	)		$	(32,115,555	)
Net loss per share, basic and diluted	$	(0.08	)		$	(0.15	)		$	(0.31	)		$	(0.43	)
Weighted average number of common shares outstanding, basic and diluted		83,599,187				83,078,675				83,434,760				74,290,598

Marker Therapeutics, Inc.Condensed Consolidated Statements of Cash Flows(Unaudited)

	For the Nine Months Ended
	September 30,
		2022				2021
Cash Flows from Operating Activities:
Net loss	$	(26,074,279	)		$	(32,115,555	)
Reconciliation of net loss to net cash used in operating activities:
Depreciation and amortization		1,975,996				1,584,495
Stock-based compensation		4,626,833				4,497,145
Amortization on right-of-use assets		739,446				757,958
Loss on disposal of assets		25,995				-
Gain on lease termination		(278,681	)			-
Changes in operating assets and liabilities:
Prepaid expenses and deposits		(181,034	)			(643,403	)
Other receivables		(1,680,782	)			1,000,316
Accounts payable and accrued expenses		(3,310,051	)			2,742,154
Related party deferred revenue		5,050,000				-
Deferred revenue		(1,146,186	)			-
Lease liability		(413,988	)			(244,752	)
Net cash used in operating activities		(20,666,731	)			(22,421,642	)
Cash Flows from Investing Activities:
Purchase of property and equipment		(1,328,664	)			(1,262,092	)
Purchase of construction in progress		(3,489,130	)			(1,519,196	)
Net cash used in investing activities		(4,817,794	)			(2,781,288	)
Cash Flows from Financing Activities:
Proceeds from issuance of common stock, net		63,573				52,552,758
Proceeds from exercise of stock options		-				3,087
Net cash provided by financing activities		63,573				52,555,845
Net (decrease) increase in cash, cash equivalents and restricted cash		(25,420,952	)			27,352,915
Cash, cash equivalents and restricted cash at beginning of the period		43,497,331				21,352,382
Cash, cash equivalents and restricted cash at end of the period	$	18,076,379			$	48,705,297

Contacts

InvestorsXuan Yangxyang@soleburystrat.com

MediaAmy Bonannoabonanno@soleburystrat.com