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Clinical Trial ● Currently Recruiting Phase III 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

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…

📅 07 May 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT07266805
Start
2025-10-16
Completion
2027-06
ClinicaliQ Trial Snapshot
  • 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 — Recruiting • Phase III • NCT07266805.
  • Trial testing oral deucrictibant tablets to prevent and treat angioedema attacks in adults with C1 inhibitor deficiency.

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What This Trial Is Studying

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. Conditions: Acquired Angioedema Due to C1-Inhibitor Deficiency (AAE-C1-INH) Interventions: Deucrictibant, Placebo, Deucrictibant, Placebo, Deucrictibant Lead Sponsor: Pharvaris Netherlands B.V. Planned Enrollment: 32 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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