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Completed Phase 3 Interventional

Study of Oral Deucrictibant Soft Capsule for On-Demand Treatment of Angioedema Attacks in Adolescents and Adults With Hereditary Angioedema

ClinicalTrials.gov ID: NCT06343779

Public ClinicalTrials.gov record NCT06343779. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 1:24 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 3, multicenter, randomized, double-blind, placebo-controlled, 2-period, 2-treatment cross-over study to evaluate the efficacy and safety of orally administered deucrictibant compared to placebo for the on-demand treatment of HAE attacks, including non-severe laryngeal attacks, in participants ≥12 to ≤75 years of age with HAE type 1, type 2, or type 3, a proportion of whom are using long-term prophylactic medication for HAE.

Study identification

NCT ID
NCT06343779
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pharvaris Netherlands B.V.
Industry
Enrollment
134 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 26, 2024 (Actual)
Primary completion
Oct 17, 2025 (Actual)
Completion
Oct 17, 2025 (Actual)
Last update posted
Nov 21, 2025

2024 – 2025

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Study Site Birmingham Alabama 35209 —
Study Site Paradise Valley Arizona 85258 —
Study Site Little Rock Arkansas 72205 —
Study Site San Diego California 92122 —
Study Site Santa Monica California 90404 —
Study Site Walnut Creek California 94598 —
Study Site Colorado Springs Colorado 80907-6231 —
Study Site Chevy Chase Maryland 20815 —
Study Site Boston Massachusetts 02115 —
Study Site Detroit Michigan 48202 —
Study Site St Louis Missouri 63141 —
Study Site Hershey Pennsylvania 17033 —
Study Site Dallas Texas 75231 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06343779, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 21, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06343779 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →