deucrictibant extended-release tablets — NDA/BLA submission
1H2027
U.S. NDA Submission: 1H2027Source filing
catalyst calendar
PHARVARIS NV · Data as of 2026-10-25
1H2027
U.S. NDA Submission: 1H2027Source filing
Q1 2027
Topline data from Part 1 of CREAATE ( NCT07266805 ), a global, pivotal Phase 3 study evaluating orally-administered deucrictibant XR for the prevention of AAE-C1INH attacks, are anticipated in the first quarter of 2027.Source filing
1Q2027
Part 1 Topline Data:1Q2027Source filing
H1 2027
Data from the CHAPTER-3 study will serve as the basis for marketing authorization applications, which are planned to be submitted starting in the first half of 2027.Source filing
Apr 23
FDA PDUFA goal April 23, 2027Source filing
Apr 23
FDA PDUFA goal April 23, 2027 U.S. ODT LaunchSource filing