Marker Therapeutics
Marker Therapeutics is a clinical-stage biopharmaceutical company developing non-genetically modified, multi-antigen recognizing T cell (MAR-T) immunotherapies for relapsed lymphoma, AML, and pancreatic cancer, with no commercial product and revenue sourced primarily from grants.
- Company typePublic
- Founded1992
- HeadquartersMinneapolis, United States
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Marker Therapeutics does
Marker Therapeutics, Inc. (NASDAQ: MRKR) is a clinical-stage biopharmaceutical company headquartered in Houston, Texas that develops non-genetically modified, multi-antigen recognizing T cell (MAR-T) immunotherapies for blood cancers and solid tumors. The company's proprietary platform — exclusively licensed from Baylor College of Medicine — selectively expands a patient's natural tumor-specific T cells from a standard blood draw, producing a product that recognizes hundreds of epitopes across up to six tumor-associated antigens (Survivin, PRAME, NY-ESO-1, MAGE-A4, SSX2, WT-1), thereby addressing tumor heterogeneity and reducing the risk of antigen-escape relapse that limits single-target CAR-T therapies.
The pipeline is anchored by MT-601, currently in the Phase 1 APOLLO multi-center study for non-Hodgkin lymphoma patients who have relapsed or are ineligible for anti-CD19 CAR-T therapy, and MT-401 in the Phase 2b ARTEMIS trial for post-transplant acute myeloid leukemia (AML), with MT-401-OTS extending the AML franchise into off-the-shelf dosing. A company-sponsored Phase 1 program in pancreatic cancer is planned for the first half of 2026 following published Baylor data showing an 84.6% disease control rate.
The business is clinical-stage with no commercial products; reported Q4 2025 revenue of approximately $1.10M derives from collaborations and grants rather than product sales, and the company posted a $12.2M net loss for full-year 2025 with $17M in cash and equivalents at year-end. Marker has secured more than $19M in non-dilutive grant funding from CPRIT, the NIH (SBIR), and the FDA, supplemented by a $25M stock purchase agreement with Lincoln Park Capital Fund (December 2022). As of March 2026 the company's market capitalization stood at roughly $22.34M. Customers today are patients enrolled in investigator-initiated and company-sponsored trials at multiple US centers; payer and provider relationships will only form upon potential regulatory approval.
Marker Therapeutics firmographics
Firmographics- Name
- Marker Therapeutics
- Legal name
- Marker Therapeutics, Inc.
- Website
- https://markertherapeutics.com
- Company type
- Public
- Founded year
- 1992
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Marker Therapeutics is a clinical-stage biopharmaceutical company developing non-genetically modified, multi-antigen recognizing T cell (MAR-T) immunotherapies for relapsed lymphoma, AML, and pancreatic cancer, with no commercial product and revenue sourced primarily from grants.
- Ownership category
- akta.pro rank
Marker Therapeutics industry classification
Industry- Product category
- Cell Therapy / T Cell Immunotherapy
- NAICS
- Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412), Scientific Research and Development Services (5417)
- SIC
- Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
- akta.pro primary industry
- CAR-T & TCR-T Therapies (HLAAABAC)
- akta.pro secondary industry
- Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies) (HLAAANAK)
Keywords
Where Marker Therapeutics is headquartered
LocationHeadquarters
- HQ city
- Minneapolis
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Marker Therapeutics business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales
Revenue model
- Pre-Revenue / Clinical Stage: Marker Therapeutics is a clinical-stage biopharmaceutical company with no commercially approved products. The company is developing T cell-based immunotherapies and has not yet generated product revenue. Current financial results show quarterly revenue of approximately $1 million primarily from collaborations or grants, with significant net losses ($12.2 million for 2025).
Go-to-market motion1 record
Distribution channels1 record
Marketing channels5 records
Marker Therapeutics product offering
Product offeringCore offering
Marker Therapeutics develops clinical-stage, non-genetically engineered, multi-antigen T cell therapies (MAR-T cells) that selectively expand natural tumor-specific T cells from a patient's blood to recognize multiple tumor antigens. Its lead product MT-601 targets six tumor antigens (Survivin, PRAME, NY-ESO-1, MAGE-A4, SSX2, WT-1) and is being evaluated in Phase 1 trials for relapsed non-Hodgkin lymphoma and pancreatic cancer. The pipeline also includes MT-401 and its off-the-shelf variant MT-401-OTS for AML.
Product overview
Marker Therapeutics is a clinical-stage biopharmaceutical company developing T cell-based immunotherapies using its proprietary MAR-T (Multi-Antigen Recognizing T cell) technology platform. The platform enables selective expansion of natural tumor-specific T cells that recognize multiple antigens without genetic modification. The core product portfolio includes MT-601 (lead candidate for lymphoma), MT-401 (for AML with both personalized and off-the-shelf versions), targeting various tumor-associated antigens including Survivin, PRAME, NY-ESO-1, MAGE-A4, SSX2, and WT-1.
Differentiator
Problem solved
Functional benefit
Products and services
- MT-601 Lead product candidate, a multi-tumor associated antigen-specific T cell product recognizing six tumor antigens (Survivin, PRAME, NY-ESO-1, MAGE-A4, SSX2, WT-1) currently evaluated in a Phase 1 APOLLO study for lymphoma patients who relapsed or are ineligible for anti-CD19 CAR-T therapy.
- MT-401 Multi-tumor associated antigen-specific T cell product for Acute Myeloid Leukemia (AML), targeting post-transplant minimal residual disease, being evaluated in Phase 2b ARTEMIS trial in combination with hypomethylating agents.
- MT-401-OTS Off-the-shelf version of MT-401 T cell product for AML treatment, with first patient treated in Q3 2025 as part of the company's off-the-shelf program.
- MAR-T Cell Technology Platform Multi-Antigen Recognizing T cell technology platform that selectively expands natural tumor-specific T cells from patient blood, capable of recognizing hundreds of epitopes within up to six tumor-associated antigens without genetic modification.
Quantifiable outcome
- 66% objective response rate (ORR) in relapsed non-Hodgkin lymphoma patients including 50% complete responses
- +3 more outcomes
Companies that use Marker Therapeutics
Customer profileSegments3 records
Ideal customer profiles3 records
Marker Therapeutics technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature4 records
Marker Therapeutics partnerships and signals
Strategic signalPartnerships
Two partnerships are on record, tiered core.
- Baylor College of MedicinecoreBaylor College of Medicine developed the MAR-T cell technology and published promising Phase 1/2 clinical trial results in Nature Medicine. Marker Therapeutics holds worldwide exclusive license for the T cell technology. Baylor is conducting pancreatic cancer research with Marker planning to initiate its own program.
- Cellipont BioservicescoreManufacturing collaboration with Cellipont Bioservices for the production of Marker Therapeutics' T cell therapy products. This partnership supports the company's manufacturing capabilities as it advances its clinical programs.
Scale indicators12 records
Recent moves6 records
Expansion highlights5 records
Marker Therapeutics competitors and assessment
Company assessmentDirect peers
- Iovance Biotherapeutics: Clinical and commercial-stage cell therapy company developing tumor-infiltrating lymphocyte (TIL) therapies for solid tumors and hematologic malignancies; directly comparable to Marker as a publicly traded cell therapy developer with overlapping hematology and oncology targets.
- Adaptimmune Therapeutics: Developer of engineered TCR-T cell therapies (Tecelra) targeting solid tumor antigens including NY-ESO-1, MAGE-A4; comparable to Marker's multi-antigen T cell strategy and similar clinical-stage commercial profile.
- Allogene Therapeutics: Allogeneic CAR-T developer with off-the-shelf platform targeting hematologic malignancies, directly relevant given Marker's MT-401-OTS off-the-shelf T cell program and shared CD19-targeting competition.
- Atara Biotherapeutics: Allogeneic T cell therapy developer (Tabelecleucel/EBVALLO) for post-HSCT lymphoproliferative disease; overlaps with Marker in cell therapy targeting hematologic malignancies and pursuing off-the-shelf T cell approaches.
- Cellectis: Clinical-stage cell therapy company developing allogeneic CAR-T (UCART) products using TALEN gene editing; comparable as a publicly traded cell therapy peer pursuing hematologic indications with off-the-shelf approaches.
- Precision BioSciences: Developer of in vivo and ex vivo gene-edited cell therapies (ARCUS platform) targeting hematologic malignancies and solid tumors; comparable clinical-stage cell therapy peer with overlapping oncology focus.
Broad incumbents
- Adaptimmune (SPEAR T-cells) vs. CAR-T players — Bristol Myers Squibb: BMS markets Breyanzi and Abecma CD19/BCMA CAR-T therapies directly competing with MT-601 in relapsed/refractory NHL and multiple myeloma; represents the incumbent standard-of-care that Marker's MAR-T must displace or follow.
- Gilead (Kite Pharma): Kite (Gilead) markets Yescarta and Tecartus CD19 CAR-T therapies, the established benchmark that Marker Therapeutics' MT-601 must compare against in the anti-CD19 CAR-T relapsed NHL setting.
Emerging players
- Cargo Therapeutics: Emerging cell therapy developer focused on engineered CAR-T approaches for hematologic malignancies including LBCL; relevant as a recent IPO-stage peer competing for the same anti-CD19 relapsed NHL space MT-601 targets.
- Caribou Biosciences: Clinical-stage allogeneic CAR-T developer (CB-010, CB-012) using CRISPR gene editing; comparable peer as a smaller publicly traded cell therapy company pursuing hematology indications and off-the-shelf platforms.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat3 records
Key risks7 records
Key highlights7 records
Customer concentration
Marker Therapeutics social profiles
Digital presenceMarker Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
Marker Therapeutics leadership team
Management profileNumber of profiles
Profiles4 records
Marker Therapeutics funding detail
Funding detailFunding overview
Funding rounds11 records
Investors4 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Marker Therapeutics M&A and investment
M&A and investmentM&A1 record
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Marker Therapeutics
What does Marker Therapeutics do?
Marker Therapeutics develops clinical-stage, non-genetically engineered, multi-antigen T cell therapies (MAR-T cells) that selectively expand natural tumor-specific T cells from a patient's blood to recognize multiple tumor antigens. Its lead product MT-601 targets six tumor antigens (Survivin, PRAME, NY-ESO-1, MAGE-A4, SSX2, WT-1) and is being evaluated in Phase 1 trials for relapsed non-Hodgkin lymphoma and pancreatic cancer. The pipeline also includes MT-401 and its off-the-shelf variant MT-401-OTS for AML.
Is Marker Therapeutics a public or private company?
Marker Therapeutics is a public company. It is classified as public and is currently operating.
When was Marker Therapeutics founded?
Marker Therapeutics was founded in 1992. It employs 11 to 50 people.
Where is Marker Therapeutics based?
Marker Therapeutics is headquartered in Minneapolis, United States, in the North America region.
How does Marker Therapeutics make money?
One revenue line is on record: pre-Revenue / Clinical Stage.
Who are Marker Therapeutics's main competitors?
Direct peers on record are Iovance Biotherapeutics, Adaptimmune Therapeutics, Allogene Therapeutics, Atara Biotherapeutics, Cellectis and Precision BioSciences. Broad incumbents are Adaptimmune (SPEAR T-cells) vs. CAR-T players — Bristol Myers Squibb and Gilead (Kite Pharma). Emerging players are Cargo Therapeutics and Caribou Biosciences.
Does Marker Therapeutics have an API?
No public API is recorded for Marker Therapeutics.
What industry is Marker Therapeutics in?
Marker Therapeutics's product category is Cell Therapy / T Cell Immunotherapy. Its primary akta.pro industry code is HLAAABAC, CAR-T & TCR-T Therapies, with a secondary code of HLAAANAK, Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies). Its NAICS code is 325414 and its SIC code is 2834.