f351

Generic: hydronidone·Code: F351

f351: developed by 1 company · 1 FDA decision. Updated within the last hour.

Development Pipeline (1)

FDA Decisions

FDA_MeetingThe company completed a Pre-New Drug Application communication meeting with the Center for Drug Evaluation of China's NMPA regarding its anti-fibrotic therapy.(GYRE)

Frequently asked questions

Who is developing f351?

f351 is being developed by GYRE THERAPEUTICS, INC..

What is f351's latest FDA decision?

The most recent tracked FDA decision for f351 is FDA_Meeting for The company completed a Pre-New Drug Application communication meeting with the Center for Drug Evaluation of China's NMPA regarding its anti-fibrotic therapy., dated January 5, 2026.

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    f351 — Drug Pipeline, Trials & FDA Status | BioSniper