Full Press Release Details
Marker Therapeutics Reports Second Quarter
2020 Operating and Financial Results
Houston, TX-August 10, 2020-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 second quarter ended June 30, 2020.
"We continue to make progress toward advancing our planned
Phase 2 trial with our novel MultiTAA-specific T cell therapy in patients with acute myeloid leukemia, or AML," said Peter
L. Hoang, President & CEO of Marker Therapeutics. "While the COVID-19 pandemic has impacted hospital systems globally,
we have augmented our process development for our MT-401 product, continued the buildout of our manufacturing facility and added
further clinical sites for our Phase 2 AML trial. With a novel cell therapy product candidate that has demonstrated the ability
to induce broad and durable immune responses in earlier clinical studies, Marker remains well-positioned to provide a potential
treatment option for patients suffering from this devastating disease."
Multi-Antigen Targeted (MultiTAA) T Cell Therapies
Phase 2 AML Trial Update
The Company continues to identify and add clinical trial sites in preparation for the Phase 2 AML trial initiation. The study is
currently subject to a partial clinical hold on the use of a new reagent in the manufacturing process until the FDA reviews
and accepts the final data and certificates of analysis for the new reagent. The alternate supplier has been delayed in providing
the reagent but expects to ship the reagent to Marker in Q3. Once Marker receives the reagent and completes the required analyses
for FDA, the Company will provide additional clarification around the timing of the AML trial enrollment.
USAN Council Approval of "Zelenoleucel" for MT-401
Marker recently announced that the United States Adopted Names
(USAN) Council approved "zelenoleucel" as the nonproprietary (generic) name for MT-401, a MultiTAA-specific T cell
product candidate for the treatment of patients with AML following allogeneic stem cell transplant in both adjuvant and active
Pancreatic Cancer Data Presented During ASCO
Updated clinical results from an ongoing investigator-sponsored
Phase 1 trial led by the Baylor College of Medicine, evaluating the Company's MultiTAA-specific T cell therapy in patients
with advanced or metastatic pancreatic adenocarcinoma, were presented during the 2020 American Society of Clinical Oncology (ASCO)
Virtual Annual Meeting. Data from a cohort of patients receiving MultiTAA-specific T cell therapy in combination with standard-of-care
chemotherapy in the first-line setting (Arm A) were presented.
On June 30, 2020, Marker announced that the Company executed
a lease agreement to establish an in-house cGMP manufacturing facility in Houston, TX. The facility is expected to be completed
by year-end and operational in 2021. Marker will continue to manufacture its MultiTAA-specific T cell therapy at the Baylor College
of Medicine to support the Company-sponsored AML trial until the in-house cGMP manufacturing facility is operational.
SECOND QUARTER 2020 FINANCIAL RESULTS
Cash Position and Guidance: At June 30, 2020, Marker
had cash and cash equivalents of $32.1 million. The Company believes that its existing cash and cash equivalents will fund its
operating expenses and capital expenditure requirements into Q2 2021.
R&D Expenses: Research and development expenses
were $4.3 million for the quarter ended June 30, 2020, compared to $3.2 million for the quarter ended June 30, 2019.
G&A Expenses: General and administrative expenses
were $2.5 million for the quarter ended June 30, 2020, compared to $2.7 million for the quarter ended June 30, 2019.
Net Loss: Marker reported a net loss of $6.3
million for the quarter ended June 30, 2020, compared to a net loss of $5.6 million for the quarter ended June 30,
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 Statement Disclaimer
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
impact of the COVID-19 pandemic; and the timing and success of our clinical trials, as well as clinical trials conducted by our
collaborators. 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
| June 30, | December 31, | |||||||
| 2020 | 2019 | |||||||
| (Unaudited) | (Audited) | |||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 32,124,187 | $ | 43,903,949 | ||||
| Prepaid expenses and deposits | 2,632,514 | 1,526,442 | ||||||
| Interest receivable | 3,440 | 56,189 | ||||||
| Total current assets | 34,760,141 | 45,486,580 | ||||||
| Non-current assets: | ||||||||
| Property, plant and equipment, net | 1,592,094 | 417,528 | ||||||
| Construction in progress | 2,629,141 | - | ||||||
| Right-of-use assets, net | 9,542,228 | 455,174 | ||||||
| Total non-current assets | 13,763,463 | 872,702 | ||||||
| Total assets | $ | 48,523,604 | $ | 46,359,282 | ||||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
| Current liabilities: | ||||||||
| Accounts payable and accrued liabilities | $ | 4,528,021 | $ | 1,757,680 | ||||
| Lease liability | 456,065 | 204,132 | ||||||
| Warrant liability | - | 31,000 | ||||||
| Total current liabilities | 4,984,086 | 1,992,812 | ||||||
| Non-current liabilities: | ||||||||
| Lease liability, net of current portion | 9,025,273 | 280,247 | ||||||
| Total non-current liabilities | 9,025,273 | 280,247 | ||||||
| Total liabilities | 14,009,359 | 2,273,059 | ||||||
| Commitments and contingencies | - | - | ||||||
| Stockholders' equity: | ||||||||
| Preferred stock - $0.001 par value, 5 million shares authorized and 0 shares issued and outstanding at June 30, 2020 and December 31, 2019, respectively | - | - | ||||||
| Common stock, $0.001 par value, 150 million shares authorized, 46.6 million and 45.7 million shares issued and outstanding as of June 30, 2020 and December 31, 2019, respectively | 46,617 | 45,728 | ||||||
| Additional paid-in capital | 374,828,385 | 371,573,909 | ||||||
| Accumulated deficit | (340,360,757 | ) | (327,533,414 | ) | ||||
| Total stockholders' equity | 34,514,245 | 44,086,223 | ||||||
| Total liabilities and stockholders' equity | $ | 48,523,604 | $ | 46,359,282 |
Marker Therapeutics, Inc.
Condensed Consolidated Statements of Operations
| For the Three Months Ended | For the Six Months Ended | |||||||||||||||
| June 30, | June 30, | |||||||||||||||
| 2020 | 2019 | 2020 | 2019 | |||||||||||||
| Revenues: | ||||||||||||||||
| Grant income | $ | 466,785 | $ | - | $ | 466,785 | $ | - | ||||||||
| Total revenues | 466,785 | - | 466,785 | - | ||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | 4,277,052 | 3,152,445 | 8,093,670 | 5,985,140 | ||||||||||||
| General and administrative | 2,547,289 | 2,721,120 | 5,374,284 | 5,526,895 | ||||||||||||
| Total operating expenses | 6,824,341 | 5,873,565 | 13,467,954 | 11,512,035 | ||||||||||||
| Loss from operations | (6,357,556 | ) | (5,873,565 | ) | (13,001,169 | ) | (11,512,035 | ) | ||||||||
| Other income (expense): | ||||||||||||||||
| Change in fair value of warrant liabilities | - | (7,000 | ) | 31,000 | (16,000 | ) | ||||||||||
| Interest income | 15,857 | 310,174 | 142,826 | 638,719 | ||||||||||||
| Net loss | $ | (6,341,699 | ) | $ | (5,570,391 | ) | $ | (12,827,343 | ) | $ | (10,889,316 | ) | ||||
| Net loss per share, basic and diluted | $ | (0.14 | ) | $ | (0.12 | ) | $ | (0.28 | ) | $ | (0.24 | ) | ||||
| Weighted average number of common shares outstanding | 46,572,739 | 45,501,078 | 46,328,561 | 45,483,513 |
Marker Therapeutics, Inc.
Condensed Consolidated Statements of Cash Flows
| For the Six Months Ended | ||||||||
| June 30, | ||||||||
| 2020 | 2019 | |||||||
| Cash Flows from Operating Activities: | ||||||||
| Net loss | $ | (12,827,343 | ) | $ | (10,889,316 | ) | ||
| Reconciliation of net loss to net cash used in operating activities: | ||||||||
| Depreciation and amortization | 124,627 | 39,811 | ||||||
| Changes in fair value of warrant liabilities | (31,000 | ) | 16,000 | |||||
| Stock-based compensation | 2,705,365 | 2,889,243 | ||||||
| Amortization on right-of-use assets | 96,973 | 89,178 | ||||||
| Changes in operating assets and liabilities: | ||||||||
| Prepaid expenses and deposits | (1,106,072 | ) | (349,750 | ) | ||||
| Interest receivable | 52,749 | 10,023 | ||||||
| Accounts payable and accrued expenses | 2,770,341 | 225,135 | ||||||
| Lease liability | (187,068 | ) | (89,907 | ) | ||||
| Net cash used in operating activities | (8,401,428 | ) | (8,059,583 | ) | ||||
| Cash Flows from Investing Activities: | ||||||||
| Purchase of property and equipment | (1,299,193 | ) | (305,382 | ) | ||||
| Purchase of construction in progress | (2,629,141 | ) | - | |||||
| Net cash used in investing activities | (3,928,334 | ) | (305,382 | ) | ||||
| Cash Flows from Financing Activities: | ||||||||
| Proceeds from exercise of stock options | - | 57,744 | ||||||
| Proceeds from exercise of warrants | 550,000 | 5,379 | ||||||
| Net cash provided by financing activities | 550,000 | 63,123 | ||||||
| Net decrease in cash | (11,779,762 | ) | (8,301,842 | ) | ||||
| Cash and cash equivalents at beginning of the period | 43,903,949 | 61,746,748 | ||||||
| Cash and cash equivalents at end of the period | $ | 32,124,187 | $ | 53,444,906 |