drugset / Trial / NCT07266805

Study of Oral Deucrictibant XR Tablet for Prophylaxis and Deucrictibant IR Capsule for On-Demand Treatment of Angioedema Attacks in Adults With Acquired Angioedema Due to C1 Inhibitor Deficiency

NCT07266805 ↗

Phase 3 Recruiting 32 enrolled Pharvaris Netherlands B.V.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 3, multicenter, 3-part study, with 2 randomized, double-blind, placebo-controlled parts and an open-label extension part, to evaluate the efficacy and safety of orally administered deucrictibant XR tablet for prophylaxis, and deucrictibant IR capsule for on-demand treatment of angioedema attacks in adult participants aged ≥ 18 years with AAE-C1INH.

Timeline

Start
2025-10-16
Primary completion
2027-06
Completion
2027-06

Drugs

EvaluationDrugModalityDoseRoute
Subject CRICTIBANT Small molecule 20 mg Oral
Subject CRICTIBANT Small molecule 40 mg Oral