MiNK Therapeutics Doses First Patient
Analysis based on 6 articles · First reported May 28, 2026 · Last updated May 28, 2026
The dosing of the first patient in the Phase 2 trial for agenT-797 by MiNK Therapeutics could significantly impact the biotechnology and pharmaceutical markets. A successful outcome could lead to a new mortality-reducing therapy for acute lung injury, potentially boosting MiNK Therapeutics' stock and attracting investment in similar immune therapies.
MiNK Therapeutics announced the dosing of the first patient in its randomized Phase 2 clinical trial (C-1300-02) evaluating agenT-797 for severe acute lung injury and critical illness. The trial, conducted in collaboration with First Lviv Territorial Medical Union and UNBROKEN Ukraine in Lviv, Ukraine, received rapid approval from the Malaysia — Ministry of Health (Malaysia). This milestone marks a significant advancement in developing a first-in-class immune therapy for conditions with high mortality and no approved treatments. Preliminary data from the trial are expected in the second half of 2026. The study aims to assess clinically meaningful ICU outcomes, including survival and ventilator-free days, and is supported by an active U.S. IND with U.S. site expansion underway.
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