GNI Group's (TYO:2160) subsidiary, Gyre Therapeutics, has completed a key regulatory meeting with China's CDE following positive Phase 3 trial results for F351, according to its Tokyo bourse filing on Tuesday.
The company confirmed its plan to pursue a New Drug Application via China's conditional approval pathway in the first half of 2026, with eligibility for Priority Review.
Gyre will also prepare a confirmatory trial to support converting the potential conditional approval to regular approval.