Study of Oral Deucrictibant Soft Capsule for On-Demand Treatment of Angioedema Attacks in Adolescents and Adults With Hereditary Angioedema (RAPIDe-3)
A Phase 3, Randomized, Double-blind, Placebo-controlled, Cross-over Study of Oral Deucrictibant Soft Capsule for On-Demand Treatment of Attacks in Adolescents and Adults With Hereditary Angioedema
Sponsor: Pharvaris Netherlands B.V.
This PHASE3 trial investigates C1 Esterase Inhibitor Deficiency and C1 Esterase Inhibitor [C1-INH] Deficiency and is currently completed. Pharvaris Netherlands B.V. leads this study, which shows 11 recorded versions since 2024 — indicating substantial longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
11 versions recorded-
Dec 2025 — Present [monthly]
Completed PHASE3
Status: Recruiting → Completed
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Sep 2025 — Dec 2025 [monthly]
Recruiting PHASE3
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May 2025 — Sep 2025 [monthly]
Recruiting PHASE3
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Feb 2025 — May 2025 [monthly]
Recruiting PHASE3
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Dec 2024 — Feb 2025 [monthly]
Recruiting PHASE3
▶ Show 6 earlier versions
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Nov 2024 — Dec 2024 [monthly]
Recruiting PHASE3
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Sep 2024 — Nov 2024 [monthly]
Recruiting PHASE3
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Aug 2024 — Sep 2024 [monthly]
Recruiting PHASE3
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Jul 2024 — Aug 2024 [monthly]
Recruiting PHASE3
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Jun 2024 — Jul 2024 [monthly]
Recruiting PHASE3
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May 2024 — Jun 2024 [monthly]
Recruiting PHASE3
First recorded
Feb 2024
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Pharvaris Netherlands B.V.
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
Amsterdam, Netherlands , Ankara, Turkey (Türkiye) , Barcelona, Spain , Berlin, Germany , Birmingham, United States , Bogotá, Colombia , Boston, United States , Box Hill, Australia , Bristol, United Kingdom , Brno, Czechia and 59 more locations