EAP for Deucrictibant Immediate-release

NCT07759141 · Status: AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2026-08-12

No results posted yet for this study

Summary

This is an expanded access program (EAP) designed to allow access to deucrictibant immediate-release (IR) capsule for eligible participants with hereditary angioedema (HAE) in the United States (US) and US territories who lack satisfactory alternative treatment options for on-demand treatment of HAE attacks, as determined by their treating physician.

Conditions

Interventions

DRUG

Deucrictibant IR

Deucrictibant IR capsule administered orally.

Sponsors & Collaborators

  • Pharvaris Netherlands B.V.

    lead INDUSTRY

Eligibility

Min Age
12 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07759141 on ClinicalTrials.gov