STOCK TITAN

MiNK Therapeutics Reports Q4 and Full Year 2025 Results; Phase 2 Programs Advance with Impactful Non-Dilutive Momentum

Rhea-AI Impact
(High)
Rhea-AI Sentiment
(Positive)

MiNK Therapeutics (NASDAQ: INKT) reported Q4 and full‑year 2025 results and highlighted multiple 2026 clinical catalysts. Key facts: cash $13.4M at year‑end, an additional $3.0M raised post‑year, net loss $12.5M for FY2025, and advancing Phase 2 ARDS and GVHD programs with near‑term readouts.

Non‑dilutive funding includes a $1.1M C‑Further collaboration, an NIH NIAID STTR grant, and the Mary Gooze award, supporting clinical starts in 1H–2H 2026.

Loading...
Loading translation...

AI-generated analysis. Not financial advice.

Positive

  • Cash balance of $13.4M at 12/31/2025 plus $3.0M raised
  • NIH NIAID STTR grant and Mary Gooze award fully fund GVHD preclinical and Phase 1 launch
  • C‑Further collaboration provides up to $1.1M in non‑dilutive funding
  • Phase 2 ARDS initiation planned 1H 2026 with readouts in 2H 2026

Negative

  • FY2025 net loss $12.5M, up from $10.8M in 2024
  • Available capital provides runway only through 2026 as disclosed

News Market Reaction – INKT

+0.10%
3 alerts
+0.10% News Effect
+2.4% Peak Tracked
-16.1% Trough Tracked
+$55K Valuation Impact
$55.25M Market Cap
0.0x Rel. Volume

On the day this news was published, INKT gained 0.10%, reflecting a mild positive market reaction. Argus tracked a peak move of +2.4% during that session. Argus tracked a trough of -16.1% from its starting point during tracking. Our momentum scanner triggered 3 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $55K to the company's valuation, bringing the market cap to $55.25M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Year-end cash: $13.4M Post-year ATM raise: $3.0M Q4 2025 net loss: $2.6M (or $0.56/share) +5 more
8 metrics
Year-end cash $13.4M Cash balance at December 31, 2025
Post-year ATM raise $3.0M Additional capital raised after year end via ATM program
Q4 2025 net loss $2.6M (or $0.56/share) Quarter ended December 31, 2025
FY 2025 net loss $12.5M (or $2.93/share) Year ended December 31, 2025 vs $10.8M in 2024
Cash used in ops 2025 $5.9M Cash used in operations 2025 vs $9.6M in 2024
ARDS market size 200,000–300,000 patients/year Hypoxemic pneumonia/ARDS patients in U.S. and major EU markets
ARDS mortality 30–40% Mortality rate in ARDS with no approved disease-modifying therapies
Median OS in R/R cancers Exceeds 23 months agenT‑797 plus commercial PD‑1 in heavily pretreated solid tumors

Market Reality Check

Price: $10.35 Vol: Volume 81,370 is well bel...
low vol
$10.35 Last Close
Volume Volume 81,370 is well below the 20-day average 871,960 (relative volume 0.09x) ahead of the results. low
Technical Shares at $10.52 are trading below the 200-day MA $13.05 and far under the $76 52-week high.

Peers on Argus

INKT fell 4.54% while close peers showed mixed moves: ACET -5.27%, ALXO -6.37%, ...
1 Up

INKT fell 4.54% while close peers showed mixed moves: ACET -5.27%, ALXO -6.37%, ARTV +7.89%, HOWL +4.31%, PRLD -0.97%, pointing to stock-specific factors rather than a uniform sector trend.

Historical Context

5 past events · Latest: Mar 17 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Mar 17 Earnings timing Positive +4.9% Set date for Q4/FY25 results and highlighted platform expansion plans.
Mar 10 Strategic collaboration Positive +29.3% C-Further deal for PRAME-targeted TCR-engineered iNKT pediatric therapy.
Mar 10 Partner pediatric program Positive +29.3% C-Further unveiled PRAME-targeted iNKT program with MiNK involvement.
Feb 03 IPF data update Positive +2.2% Keystone data showing significant iNKT depletion in end-stage IPF lungs.
Jan 08 GVHD trial launch Positive -1.7% Announcement of Phase 1 allo‑iNKT trial for GVHD prevention with non-dilutive support.
Pattern Detected

Recent news with positive clinical or partnership themes has usually seen aligned positive price moves, with only one noted divergence.

Recent Company History

Over the past six months, INKT has highlighted several platform-building milestones. A Jan 2026 GVHD Phase 1 trial announcement and Feb 2026 IPF data update reinforced its allo‑iNKT strategy. In Mar 2026, collaboration news with C‑Further around PRAME‑targeted pediatric oncology programs, plus an earnings-date announcement on Mar 17, were followed by positive price reactions. Today’s Q4/FY25 earnings and pipeline update continue that narrative of non‑dilutive funding, expanding indications, and clinical progression into 2026.

Regulatory & Risk Context

Active S-3 Shelf · $150,000,000
Shelf Active
Active S-3 Shelf Registration 2025-11-07
$150,000,000 registered capacity

An effective S-3 shelf filed on Nov 7, 2025 registers up to $150,000,000 of mixed securities, including an ATM program for up to $50,000,000 of common stock through B. Riley Securities. Under Instruction I.B.6 and a public float of $35,031,699, current ATM capacity is $6,641,284. The ATM carries a 3.0% sales commission, with stated use of proceeds for working capital, R&D, clinical programs, collaborations, and capital spending.

Market Pulse Summary

This announcement combines Q4/FY25 financials with a detailed roadmap of 2026 catalysts across ARDS,...
Analysis

This announcement combines Q4/FY25 financials with a detailed roadmap of 2026 catalysts across ARDS, IPF, oncology, and GVHD, supported by non‑dilutive awards and C‑Further collaboration funding of up to $1.1M. Investors may track cash usage versus the $13.4M year‑end balance and the $12.5M 2025 net loss, along with timing of Phase 2 ARDS initiation, GVHD Phase 1 readouts, and potential use of the $50,000,000 ATM registered under the $150,000,000 shelf.

Key Terms

graft-versus-host disease, phase 2 trial, phase 1, median os, +4 more
8 terms
graft-versus-host disease medical
"fully fund graft-versus-host disease (GVHD) preclinical data with clinical trial"
Graft-versus-host disease is a complication that can occur after a transplant using donor immune cells, where those transplanted cells attack the recipient’s organs and skin instead of protecting them; imagine a new security team mistaking the building’s occupants for intruders. It matters to investors because its likelihood, severity, and available treatments shape clinical trial results, drug approval chances, safety labels, patient outcomes, and the commercial potential of therapies aimed at preventing or managing the condition.
phase 2 trial medical
"ARDS / hypoxemic pneumonia Phase 2 trial initiation 1H 2026; early data"
A phase 2 trial is an intermediate-stage clinical study that tests whether a new treatment works and is reasonably safe in a group of patients who have the condition it targets. Think of it as a field test of a prototype product: it checks real-world effectiveness and side effects on a modest number of users to decide whether the treatment should move to larger, definitive testing. Investors watch phase 2 results because positive outcomes can sharply increase the likelihood of regulatory approval and future sales, while failures often halt development.
phase 1 medical
"operations for the Phase 1. Trial is advancing through university approval"
Phase 1 is the first stage of testing a new drug or medical treatment in people, focused primarily on safety, how the body handles the product, and finding a tolerated dose. Think of it as a short, tightly controlled experiment with a small group to check for dangerous side effects before wider testing; for investors it is an early milestone that reduces some uncertainty but still carries high risk and potential for both big value changes and setbacks.
median os medical
"Median OS in R/R cancers exceeded 23 months in combo with commercial PD-1"
Median overall survival (median OS) is the midpoint time after a treatment or diagnosis when half of the patients in a study are still alive and half have died. It gives a single, easy-to-compare measure of how long a therapy tends to extend life, and investors use it to judge a drug’s clinical benefit, potential regulatory approval, and commercial value—similar to comparing how long different batteries typically last before half of them fail.
at the market sales agreement financial
"we executed and implemented an at the market sales agreement and ended"
An at the market sales agreement lets a company authorize a broker to sell newly issued shares directly into the open market at prevailing prices, rather than selling a large block all at once. Investors should care because it provides a flexible way for a company to raise cash but can increase the number of shares available and put downward pressure on the stock price, similar to a store quietly adding more items for sale at current shelf prices.
non-dilutive funding financial
"Consortium collaboration adds to growing non-dilutive funding for PRAME-TCR"
Non-dilutive funding is money a company raises that does not require issuing new shares or reducing existing owners’ percentage ownership, such as grants, certain loans, contract revenue, or licensing deals. It matters to investors because it lets a company finance growth or research without shrinking shareholder stakes or changing control, much like topping up a car’s gas tank instead of selling part of the car to pay for the trip.
allogeneic medical
"pioneering allogeneic invariant natural killer T (allo-iNKT) cell therapies"
Allogeneic describes a process or material involving different individuals of the same species, such as cells, tissues, or organs donated from one person to another. It is important to investors because products or treatments based on allogeneic sources can enable scalable, off-the-shelf solutions, potentially reducing costs and increasing accessibility in healthcare and biotech industries.
tumor microenvironment medical
"reprogramming the tumor microenvironment through dendritic cell activation"
The tumor microenvironment is the immediate area surrounding a cancer cell, made up of nearby cells, blood vessels, and support structures that influence how the cancer grows and spreads. It functions like a bustling neighborhood that can either help or hinder the tumor’s development. For investors, understanding changes in this environment can signal the effectiveness of treatments and potential shifts in a cancer-related market.

AI-generated analysis. Not financial advice.

  • ARDS / hypoxemic pneumonia Phase 2 trial initiation 1H 2026; early data by year end; market opportunity of ~200,000–300,000 patients annually in US/EU
  • C-Further Consortium collaboration adds to growing non-dilutive funding for PRAME-TCR iNKT in pediatric oncology
  • NIH STTR grant and Mary Gooze philanthropic award fully fund graft-versus-host disease (GVHD) preclinical data with clinical trial launch in 1H 2026
  • Keystone Symposia data report iNKT depletion in end-stage Pulmonary Fibrosis (IPF); underscores pipeline expansion
  • Portfolio focused on high-value immune restoration with multiple 2026 clinical catalysts

NEW YORK, March 31, 2026 (GLOBE NEWSWIRE) -- MiNK Therapeutics, Inc. (NASDAQ: INKT), a clinical-stage biopharmaceutical company pioneering allogeneic invariant natural killer T (allo-iNKT) cell therapies to restore immune balance and treat immune-mediated diseases and cancer, today reported financial results for the fourth quarter and full year ended December 31, 2025.

“2025 was a foundational year in which we sharpened our focus on immune restoration in auto-immune and inflammatory diseases and began to see the power of strategic, non-dilutive partnerships accelerate our progress,” said Jennifer Buell, PhD, President and Chief Executive Officer of MiNK Therapeutics. “We are deliberately building a pipeline where iNKT cells address serious auto-immune and inflammatory conditions — from acute critical care in ARDS to chronic fibrotic disease in IPF and immune dysregulation in GVHD. The C-Further collaboration, together with the NIH NIAID STTR grant and Mary Gooze philanthropic award secured in 2025 for our GVHD program, reflects growing recognition of our platform’s potential. We enter 2026 with strong momentum and multiple near-term opportunities to demonstrate clinical value.”

Terese Hammond, MD, Head of Pulmonary and Inflammatory Diseases at MiNK, added: “There is a clear continuum from acute inflammation and autoimmune dysregulation to chronic fibrotic diseases like IPF and even immune-resistant cancers. MiNK’s iNKT platform is uniquely suited to address this spectrum because of its ability to deliver context-dependent immune modulation — activating anti-tumor responses in cancer while restoring balance and suppressing harmful inflammation in acute and chronic lung disease.”

2025 Achievements and 2026 Milestones

Pulmonary & Critical Care: Large Market Opportunity with Near-Term Catalysts
agenT-797 advances in randomized Phase 2 in hypoxemic pneumonia/ARDS, a severe inflammatory condition affecting ~200,000–300,000 patients annually in the U.S. and major European markets. With mortality rates of 30–40% and no approved disease-modifying therapies, ARDS represents a substantial commercial opportunity with strong government and biodefense alignment.

  • Phase 2 clinical readouts planned for 2H 2026
  • Expanded development into end stage pulmonary fibrosis (IPF)
  • Data presented at Keystone Symposia demonstrated significant iNKT cell depletion in end-stage IPF
  • Strategic discussions to advance agent-797 in IPF are actively underway

Oncology: Durable Responses in Checkpoint-Resistant Tumors
Data presented at SITC 2025 reinforced agenT-797’s ability to deliver durable clinical benefit in heavily pretreated, checkpoint-refractory solid tumors.

  • Median OS in R/R cancers exceeded 23 months in combo with commercial PD-1 therapy
  • Complete remissions lasting beyond two years, long-term survival across multiple tumors
  • Translational analyses showed iNKT cells actively reprogramming the tumor microenvironment through dendritic cell activation, macrophage repolarization, and reinvigoration of exhausted T cells

Transplantation: Externally Funded GVHD Program Advancing
NIH STTR grant from the National Institute of Allergy and Infectious Diseases (NIAID) supports development and evaluation of agenT-797 in preclinical models while The Mary Gooze Clinical Trial Award to the University of Wisconsin–Madison directly funds enrollment, immune monitoring, and operations for the Phase 1.

  • Trial is advancing through university approval with first dosing expected May 2026
  • Preliminary clinical data expected 2H 2026
  • Program represents clinically meaningful opportunity with minimal capital burden.

Expanding Pipeline: Targeting Resistance and Expanding Reach

  • PRAME-TCR-engineered iNKT advancing under the C-Further Consortium collaboration
    • Collaboration provides up to $1.1 million in non-dilutive funding plus meaningful double-digit percentage revenue share.

Leadership and Operational Readiness

  • Dr. Terese Hammond appointed Head of Pulmonary and Inflammatory Diseases
  • Col. (Ret.) John Holcomb, MD added to the Board of Directors and Scientific Advisory Board
  • Melissa Orilall appointed Principal Financial Officer
  • Manufacturing is optimized in Lexington and Boston sites

With the scale and complexity of the work we are now undertaking, including randomized clinical execution, multi-program advancement, and increasing external engagement, we have also strengthened our financial leadership with the recent appointment of Melissa Orillal as Principal Financial Officer. Melissa brings deep experience in financial operations, planning, and disciplined execution, including her work at the Whitehead Institute and in corporate banking. Her focus is on ensuring that our capital allocation, reporting, and operational execution remain tightly aligned as we advance through this next phase. This is an important step as we transition from an early-stage development company into a more execution-driven clinical-stage biopharmaceutical company.

These 2025 achievements — robust scientific validation, non-dilutive capital inflows, and operational strengthening, position MiNK for a catalyst-rich 2026, including ARDS Phase 2 initiation, GVHD clinical data, multiple scientific presentations, and continued partnership momentum.

Financial Highlights

During 2025 we executed and implemented an at the market sales agreement and ended the year with a cash balance of $13.4 million. Since year end, we have raised an additional $3.0 million through this program, providing a runway through 2026. Our net loss for the quarter ended December 31, 2025, was $2.6 million, or $0.56 per share, compared to $2.5 million, or $0.62 per share for Q4 2024. For the year ended December 31, 2025, our net loss was $12.5 million, or $2.93 per share, compared to $10.8 million, or $2.86 per share, for the year ended December 31, 2024.

Summary Consolidated Financial Information 
         
Condensed Consolidated Balance Sheet Data 
(in thousands) 
(unaudited) 
         
 December 31, 2025December 31, 2024    
         
Cash and cash equivalents$13,360 $4,577     
         
         
         
Other Financial Information 
(in thousands) 
(unaudited) 
         
 Three months ended December 31, Year ended December 31, 
  2025  2024  2025  2024 
         
Net loss$2,602 $2,464 $12,494 $10,785 
Net loss per share 0.56  0.62  2.93  2.86 
         
Cash used in operations$2,074 $1,728 $5,925 $9,555 
         


Conference Call and Webcast Information 
United States - New York
USA & Canada - Toll-Free
Conference ID -
(646) 307-1963
(800) 715-9871
6761941


Webcast & Replay Information

A live webcast and replay of the conference call will be accessible from the Events & Presentations page of the Company’s website following the event.

Live event link: https://edge.media-server.com/mmc/p/6xxeh8o5
Webcast Replay: https://investor.minktherapeutics.com/events-and-presentations

About MiNK Therapeutics

MiNK Therapeutics is a clinical-stage biopharmaceutical company pioneering the development of allogeneic invariant natural killer T (iNKT) cell therapies and precision immune modulators designed to restore immune balance and drive durable cytotoxic responses. MiNK’s proprietary iNKT platform bridges innate and adaptive immunity to address cancer, autoimmune disease, and immune collapse.

Its lead candidate, agenT-797, is an off-the-shelf, cryopreserved iNKT cell therapy currently in clinical trials for solid tumors, graft-versus-host disease (GvHD), and critical pulmonary immune failure. MiNK’s pipeline also includes TCR-based and neoantigen-targeted iNKT programs that enable tissue-specific immune activation. With a scalable manufacturing process and broad therapeutic potential, MiNK is advancing a new class of immune reconstitution therapies designed to deliver durable, accessible, and globally deployable treatments.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the federal securities laws, including statements regarding the potential, safety, clinical benefit, and development plans for agenT-797 and other iNKT-based therapies. These statements involve risks and uncertainties, including those described under “Risk Factors” in MiNK’s most recent SEC filings. MiNK undertakes no obligation to update these statements except as required by law.

Contacts

Investor Contact: 917-362-1370 | investor@minktherapeutics.com
Media Contact: 781-674-4428 | communications@minktherapeutics.com

Source: MiNK Therapeutics


FAQ

When will MiNK Therapeutics (INKT) begin the Phase 2 ARDS trial?

MiNK plans to initiate the randomized Phase 2 ARDS trial in 1H 2026. According to MiNK Therapeutics, readouts from the Phase 2 are expected in 2H 2026, targeting hypoxemic pneumonia/ARDS patients.

What funding supports MiNK's GVHD program and when will clinical dosing start?

The GVHD program is funded by an NIH NIAID STTR grant and the Mary Gooze award. According to MiNK Therapeutics, university approvals are underway with first dosing expected in May 2026 for the Phase 1 trial.

How much non‑dilutive funding does the C‑Further collaboration provide to MiNK (INKT)?

The collaboration offers up to $1.1 million in non‑dilutive funding plus revenue share. According to MiNK Therapeutics, the agreement includes a meaningful double‑digit percentage revenue share on PRAME‑TCR iNKT.

What were MiNK Therapeutics' (INKT) cash and loss figures for FY2025?

MiNK reported $13.4 million in cash and a net loss of $12.5 million for FY2025. According to MiNK Therapeutics, an additional $3.0 million was raised post‑year via an ATM program.

What near‑term clinical readouts and milestones should investors expect from INKT in 2026?

Investors should expect ARDS Phase 2 readouts in 2H 2026 and preliminary GVHD clinical data in 2H 2026. According to MiNK Therapeutics, multiple scientific presentations and program advancements are planned across 2026.