Mink Therapeutics doses first patient in Phase 2 agenT-797 acute lung injury trial

PUBT·05/28/2026 13:10:55

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Mink Therapeutics dosed the first patient in a randomized Phase 2 trial of agenT-797 for severe acute lung injury meeting global ARDS criteria.
Study compares agenT-797 with standard of care versus placebo with standard of care in critically ill ICU patients.
Results have not been presented; preliminary data are expected in the second half of 2026.
Trial aims to show whether the therapy can improve ICU recovery and survival outcomes in a setting with no mortality-reducing treatments.
Program expands the company’s iNKT cell platform into critical care, with U.S. IND-backed plans to add sites.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Mink Therapeutics Inc. published the original content used to generate this news brief on May 28, 2026, and is solely responsible for the information contained therein.

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