Developer docs
API playgroundTry for free, no card

Search company profiles

Marker Therapeutics

Full company profile

uuid00032pk

Namestring
Marker Therapeutics
Legal namestring
Marker Therapeutics, Inc.
Company typeenum
Public
Founded yearint
1992
Descriptiontext

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.

Short descriptiontext

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.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersMinneapolis, United States
HQ citystring
Minneapolis
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
T cell immunotherapy, cell therapy platform, multi-antigen therapy, clinical-stage biopharmaceutical, adoptive cell therapy
Industry2 codes
1CAR-T & TCR-T Therapies
CodeHLAAABACPrimaryYes
2Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies)
CodeHLAAANAKPrimaryNo
NAICS code3 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
  • Scientific Research and Development Services5417
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Cell Therapy / T Cell Immunotherapy
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pre-Revenue / Clinical Stage
TypeSubscription Recurring
Description

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).

defenseworld.net
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

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.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 66% objective response rate (ORR) in relapsed non-Hodgkin lymphoma patients including 50% complete responses
+3 more records
Product overview1 text field

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.

Product and service4 records
1MT-601
CategoryT Cell Therapy
Description

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.

2MT-401
CategoryT Cell Therapy
Description

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.

3MT-401-OTS
CategoryT Cell Therapy
Description

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.

4MAR-T Cell Technology Platform
CategoryTechnology Platform
Description

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.

Scale indicator12 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-01-05
Description

Baylor 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.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-01-01
Description

Manufacturing 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.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeEmerging player
Description

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.

TypeEmerging player
Description

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

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles4 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds11 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors4 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Marker Therapeutics

Cell Therapy / T Cell Immunotherapymarkertherapeutics.com

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.

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

  • T cell immunotherapy
  • Cell therapy platform
  • Multi-antigen therapy
  • Clinical-stage biopharmaceutical
  • Adoptive cell therapy

Where Marker Therapeutics is headquartered

Location

Headquarters

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

  1. 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 offering

Core 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 profile

Segments3 records

Ideal customer profiles3 records

Marker Therapeutics technology and API

Technology

Technology 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 signal

Partnerships

Two partnerships are on record, tiered core.

  • Baylor College of MedicinecoreStrategic or Co-development Partner · 5 January 2026Baylor 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 BioservicescoreTechnology or Integration · 1 January 2025Manufacturing 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 assessment

Direct 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 presence

Marker Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Marker Therapeutics leadership team

Management profile

Number of profiles

Profiles4 records

Marker Therapeutics funding detail

Funding detail

Funding 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 investment

M&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.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
Markets DailyMarker Therapeutics, Inc. (NASDAQ:MRKR) Stock Short Interest Jumps 62.8%Short interest in Marker Therapeutics rose 62.8% to 226,620 shares as of September 15th. The stock opened at $1.05, and the company reported a quarterly EPS of -$0.09, beating estimates of -$0.25. Analysts have a consensus 'Hold' rating with a $10.00 price target.Ticker ReportMarker Therapeutics, Inc. (NASDAQ:MRKR) Short Interest UpdateShort interest in Marker Therapeutics rose 62.8% to 226,620 shares as of September 15th, with Renaissance Technologies increasing its stake by 41.8% in Q1. Analysts rate the stock a Hold with a $10 price target, and the company reported a loss of $0.09 per share for the quarter.American Banking and Market NewsQ3 EPS Forecast for Marker Therapeutics Boosted by AnalystAnalysts at HC Wainwright raised their Q3 2026 earnings per share estimates for Marker Therapeutics, anticipating narrower losses compared to previous forecasts. The firm maintained a 'Buy' rating on the stock while Weiss Ratings upgraded its rating from 'sell (e+)' to 'sell (d-)'. Despite these near-term estimate revisions, longer-term projections indicate continued losses through FY2030.YahooUS High Growth Tech Stocks To Watch For Potential ExpansionThe article presents a list of high-growth technology stocks in the United States, highlighting companies such as Marker Therapeutics, Palantir Technologies, and Reddit based on their revenue and earnings growth. It provides detailed financial analysis for specific entities like ADMA Biologics and Roku, including market capitalization, revenue breakdowns, and future projections. The content serves as an investment screening report rather than reporting on a specific corporate event or transaction.Defense WorldMarker Therapeutics, Inc. (NASDAQ:MRKR) Given Consensus Recommendation of “Moderate Buy” by BrokeragesFive analysts covering Marker Therapeutics, Inc. (NASDAQ:MRKR) have assigned a consensus rating of "Moderate Buy" with an average 1-year price target of $11.25, with ratings ranging from sell to strong buy. Multiple hedge funds and institutional investors recently acquired or increased stakes in the company, with institutional ownership now at 22.39% of shares. The company reported quarterly earnings of -$0.04 per share, beating the consensus estimate of -$0.21 by $0.17, while posting revenue of $1.10 million against a $0.68 million consensus estimate.Defense WorldMarker Therapeutics (MRKR) to Release Quarterly Earnings on MondayMarker Therapeutics (NASDAQ:MRKR) is scheduled to release its Q4 2025 earnings before the market opens on Monday, March 30th, with analysts estimating a loss of $0.21 per share on revenue of $1.0040 million. The company's most recent reported quarter (Q3 2025) showed earnings of ($0.04) per share, beating consensus estimates by $0.17, though Marker Therapeutics remains unprofitable with a negative net margin of 343.03%. The article provides analyst ratings, institutional ownership data, and price targets ranging from $10.00 to $11.25, reflecting ongoing market coverage of the clinical-stage biopharmaceutical company.Defense WorldQ1 Earnings Estimate for MRKR Issued By HC WainwrightHC Wainwright issued Q1 2027 earnings per share estimates for Marker Therapeutics on March 20th, forecasting a loss of ($0.33) per share for the quarter, while maintaining a "Buy" rating with a $10.00 price target. The article also covers recent Q4 earnings where Marker Therapeutics beat estimates with a ($0.04) loss versus the ($0.21) consensus estimate, along with multiple analyst rating changes and institutional investor activity in the stock.Defense WorldQ2 Earnings Estimate for MRKR Issued By Brookline Cap MBrookline Cap M issued Q2 2026 earnings estimates for Marker Therapeutics, with analysts forecasting a loss per share of ($0.27) and revenues of $1.10 million. The company recently reported a quarterly loss of ($0.04) per share, exceeding analyst expectations, and had a market cap of $22.34 million. Several institutional investors have increased their stake in the company.GlobeNewswireMarker Therapeutics Reports Year-End 2025 Corporate and Financial ResultsMarker Therapeutics reported year-end 2025 corporate and financial results, highlighting Phase 1 APOLLO data showing a 66% objective response rate in relapsed non-Hodgkin lymphoma including 50% complete responses, and a 78% ORR in Hodgkin lymphoma with a favorable safety profile. The company also announced research published in Nature Medicine demonstrating promising multi-antigen T cell results in pancreatic cancer with up to 84.6% disease control rate, and entered a manufacturing collaboration with Cellipont Bioservices for cGMP production of MT-601. Financially, Marker reported a cash position of $17 million, R&D expenses of $11.8 million, and a net loss of $12.2 million for 2025.Stock TitanMarker Therapeutics cash runway extends to Q4 2026Marker Therapeutics reported year-end 2025 corporate and financial results, with Phase 1 APOLLO data showing a 66% objective response rate in relapsed non-Hodgkin lymphoma and research published in Nature Medicine demonstrating promising results in pancreatic cancer. The company ended 2025 with $17 million in cash, extending its runway to Q4 2026, while reporting a net loss of $12.2 million compared to $10.7 million in 2024. Marker also strengthened its manufacturing capabilities through a collaboration with Cellipont Bioservices and expanded its Board with the appointment of Kathryn Penkus Corzo.