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NCT07046806: BK-AE-nC1INH

Oral Deucrictibant for Prophylactic and Acute Treatment in Hereditary Angioedema Patients

Recruiting now Phase 1, PHASE2 Last updated 2 July 2025
What this trial tests

Phase 1, PHASE2 trial testing Deucrictibant XR tablet in Hereditary Angioedema (HAE) in 10 participants. Currently enrolling.

Timeline
10 March 2025
Primary endpoint
1 April 2026
1 April 2026

Quick facts

Lead sponsorInstitute for Asthma and Allergy
PhasePhase 1, PHASE2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingtriple
Primary purposeprevention
Enrollment10
Start date10 March 2025
Primary completion1 April 2026
Estimated completion1 April 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Institute for Asthma and Allergy

Who can join

Adults 18 to 75, any sex, with Hereditary Angioedema (HAE) or Angioedema. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To assess the efficacy of prophylactic treatment with deucrictibant extended release (XR) tablet versus placebo in preventing angioedema attacks, and to also assess the efficacy of deucrictibant soft capsules as on-demand treatment versus placebo in achieving angioedema symptom relief during acute attacks.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hereditary Angioedema (HAE)

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07046806.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing