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Financial Snapshot

Revenue
TTM
$3.949M
Gross Margin
Last 4 Quarters
N/A
Net Income
TTM
-$10.90M
Current Assets
2026 Q1
Current Liabilities
2026 Q1
Current Ratio
2026 Q1
479.21%
Total Assets
2026 Q1
Total Liabilities
2026 Q1
Book Value
2026 Q1
13.80M
Cash
2026 Q1
P/E
Last 4 Quarters
N/A
Free Cash Flow
Last 4 Quarters
N/A

Stock Price

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Market Cap: $23.676 Million

About Marker Therapeutics Inc

Marker Therapeutics (NASDAQ: MRKR) is a clinical-stage biopharmaceutical company developing non-genetically engineered T cell therapies for cancer. The company generates no product revenue as of FY2025, funding operations through grant income from government agencies and non-profit foundations under cost-reimbursement arrangements, along with equity offerings via an at-the-market (ATM) agreement. Its lead product, MT-601, is a multiTAA-specific T cell therapy being developed for lymphoma, with a pivotal trial (APOLLO study) anticipated to commence in 2026. Manufacturing of MT-601 is conducted through third-party CDMOs, including Baylor College of Medicine (BCM) for ongoing clinical supply and Cellipont Bioservices under a Statement of Work entered June 16, 2025 for scale-up and cGMP production. The company has incurred recurring losses, pays no dividends, and lists common stock on the Nasdaq Capital Market under the symbol MRKR. As of March 16, 2026, the stock traded at $1.41 per share with 39 stockholders of record.

Revenue model
Grant income recognized on a cost-reimbursement basis from government agencies and non-profit foundations as qualifying research and development expenses are incurred. No product revenue was generated during the two years ended December 31, 2025. Additional funding comes from equity issuances under an ATM agreement.
Products and services
MT-601: a non-genetically engineered, multiTAA-specific T cell (MAR-T cell) therapy in clinical development for lymphoma. No products are approved or commercialized as of the FY2025 10-K filing.
Customers and end markets
No commercial customers as of FY2025. End market is oncology, specifically lymphoma patients. Funding counterparties are government agencies and non-profit foundations providing research grants.
Value-chain role
Clinical-stage drug developer. Relies on third-party CDMOs for manufacturing: BCM supplies clinical trial material; Cellipont Bioservices engaged via Statement of Work (June 16, 2025) for technology transfer and cGMP manufacturing to support the APOLLO pivotal study.

Source: SEC 10-K, filed 2026-03-18

Industry: Pharmaceutical Preparations Peers: ABVC Biopharma Inc Spyre Therapeutics Inc Aptinyx Inc. Neurogene Inc Aravive, Inc. Avalo Therapeutics Inc Comera Life Sciences Holdings, Inc. Maia Biotechnology Inc Oragenics Inc

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