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NCT06679881 · ClinicalTrials.gov registry record · Phase 3

Long-Term, Open-label Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE

A Phase 3 study of Hereditary Angioedema (HAE), sponsored by Pharvaris Netherlands B.V..

Recruiting
Registry status
Phase 3
Development phase
170
Enrollment target
20
Study locations

NCT06679881: Recruiting Phase 3 study of Hereditary Angioedema (HAE), sponsored by Pharvaris Netherlands B.V..

NCT06679881 is a Phase 3 study of Hereditary Angioedema (HAE) that is actively recruiting participants, run by Pharvaris Netherlands B.V.. The registered enrollment target is 170 participants, above the 43-participant average among 7 other Hereditary Angioedema (HAE) trials with a reported enrollment target (295% higher). The trial reports 20 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06679881, a Phase 3 study of Hereditary Angioedema (HAE), is actively recruiting participants, sponsored by Pharvaris Netherlands B.V..

RECRUITING
Registry status
Phase 3
Development phase
170 participants
Enrollment target
20
Study locations

Study Summary

This is a Phase 3, multicenter, long-term, open-label study to evaluate the safety and efficacy of once-daily orally administered deucrictibant extended-release tablet for prophylaxis to prevent angioedema attacks in participants aged ≥12 years with Hereditary Angioedema

Interventions

  • DRUG Deucrictibant

Study Locations (20)

Other

  • Study Site - Melbourne
  • Study Site - Melbourne
  • Study Site - Perth
  • Study Site - Vienna
  • Study Site - Sofia
  • Study Site - Montreal
  • Study Site - Berlin
  • Study Site - Frankfurt
  • Study Site - Hong Kong
  • Study Site - Dublin
  • Study Site - Padua
  • Study Site - Krakow
  • Study Site - Cape Town
  • Study Site - Daegu
  • Study Site - Seoul
  • Study Site - Barcelona
  • Study Site - Brighton

California

  • Study Site - Santa Monica
  • Study Site - Walnut Creek

Missouri

  • Study Site - St Louis

Trial Details

FieldValue
Enrollment Target 170 participants
Start Date 2025-02-01
Est. Completion 2028-12
Phase Phase 3
Pharvaris Netherlands B.V.

6 total trials

What NCT06679881 shows while recruiting

NCT06679881 is an interventional study that assigns participants to a tested intervention. The registered 170 participants enrollment target is mid-sized for trials with a published cap, above the 43-participant average among 7 other Hereditary Angioedema (HAE) trials with a reported enrollment target (295% higher).

The record links to 1 condition, with Hereditary Angioedema (HAE) appearing as the primary indexed condition, and to 1 intervention - of which Deucrictibant is the first listed.

NCT06679881 names 20 study sites across 3 states, led by Other, California, Missouri.

Frequently Asked Questions

What is clinical trial NCT06679881 about?

NCT06679881 is a clinical study titled "Long-Term, Open-label Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE". This is a Phase 3, multicenter, long-term, open-label study to evaluate the safety and efficacy of once-daily orally administered deucrictibant extended-release tablet for prophylaxis to prevent angioedema attacks in participants aged ≥12 years with Hereditary Angioedema

What is the current status of trial NCT06679881?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 170 participants. The study started on 2025-02-01. Estimated completion is 2028-12.

What conditions does trial NCT06679881 study?

This clinical trial studies the following conditions: Hereditary Angioedema (HAE).

What interventions are being tested in trial NCT06679881?

The interventions under investigation include: Deucrictibant (DRUG).

Who is sponsoring clinical trial NCT06679881?

This trial is sponsored by Pharvaris Netherlands B.V., which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06679881 being conducted?

This trial has 20 study locations across California, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06679881, the US trial registry maintained by the National Library of Medicine. NCT06679881 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.