$INKT

MiNK Therapeutics, Inc.

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MiNK Therapeutics Selected for ARPA-H-Funded Initiative to Advance Room-Temperature Cell Therapy

MiNK Therapeutics (INKT) was selected for ARPA-H's BoSS program, which aims to develop room-temperature storage for cell therapies. The company will receive funding as part of a team led by Draper Lab, focusing on its agenT-797 iNKT platform. ARPA-H committed up to $87 million for the four-year program, aiming to reduce cold-chain dependence and expand access to cell-based medicines.

MiNK Therapeutics Reports Second Quarter 2026 Financial Results and Reports Observations from Randomized Phase 2 Trial of agenT-797 in Acute Lung Injury

MiNK Therapeutics, Inc. (INKT) filed an SEC Form 8-K — Results of Operations and Financial Condition. MiNK Therapeutics Reports Second Quarter 2026 Financial Results and Reports Observations from Randomized Phase 2 Trial of agenT-797 in Acute Lung Injury • First patients treated in randomized Phase 2 trial C-1300-02 were alive at Day 28, with improved oxygenation, infection contr

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MiNK Therapeutics Selected for ARPA-H-Funded Initiative to Advance Room-Temperature Cell Therapy

MiNK Therapeutics (INKT) was selected for ARPA-H's BoSS program, which aims to develop room-temperature storage for cell therapies. The company will receive funding as part of a team led by Draper Lab, focusing on its agenT-797 iNKT platform. ARPA-H committed up to $87 million for the four-year program, aiming to reduce cold-chain dependence and expand access to cell-based medicines.

$INKTMed

MiNK Therapeutics Reports Second Quarter 2026 Financial Results and Reports Observations from Randomized Phase 2 Trial of agenT-797 in Acute Lung Injury

MiNK Therapeutics, Inc. (INKT) filed an SEC Form 8-K — Results of Operations and Financial Condition. MiNK Therapeutics Reports Second Quarter 2026 Financial Results and Reports Observations from Randomized Phase 2 Trial of agenT-797 in Acute Lung Injury • First patients treated in randomized Phase 2 trial C-1300-02 were alive at Day 28, with improved oxygenation, infection contr

$INKTLow

MiNK Therapeutics, Inc. (INKT): Submission of Matters to a Vote of Security Holders

MiNK Therapeutics, Inc. (INKT) filed an SEC Form 8-K — Submission of Matters to a Vote of Security Holders. 8-K 0001840229 false 0001840229 2026-06-17 2026-06-17 UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Report (Date of earliest event reported): June 17,

$SPRCMedAI 8/10

Top Biotech Gainers: SPRC Deal Gets Nod, CODX Rallies, OTLK, AKTX, FTRE Drawing Investor Interest

SciSparc (SPRC) shares rose ~140% after its TSX Venture subsidiary received conditional approval to buy ~54% of private Israeli CliniQuantum for 56.6M NeuroThera shares (~$9.46M). Co-Diagnostics (CODX) gained ~53% for a third day amid Ebola PCR assay progress. Akari (AKTX) jumped ~38% on ASCO abstract acceptance and new KRAS-mutant synergy data; Outlook (OTLK) rose ~26% ahead of a June FDA resubmission.

$INKTMed

Biotech MiNK targets up to 300,000 ARDS patients as Phase 2 starts

MiNK Therapeutics reported its Q4 and full-year 2025 financial results, highlighting a cash balance of $13.4 million and advancing its Phase 2 ARDS and GVHD programs. The company plans to initiate its Phase 2 ARDS trial in the first half of 2026, targeting 200,000-300,000 patients annually in the US and EU, with clinical readouts expected in the second half of 2026. MiNK is also benefiting from non-dilutive funding, including a $1.1 million collaboration with C-Further and grants for its GVHD program.

MiNK Therapeutics to begin phase 1 trial of iNKT cell therapy for GvHD

MiNK Therapeutics will initiate a Phase 1 clinical trial for its lead therapy, agenT-797, to evaluate its potential in reducing graft-versus-host disease (GvHD) and other complications in patients with high-risk leukemias and blood cancers. The therapy is an off-the-shelf allogeneic invariant natural killer T (iNKT) cell therapy that has previously shown safety and immune-modulating activity. This trial marks the company's expansion into transplantation medicine, aiming to suppress inflammatory immune responses while preserving anti-leukemia activity.

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