CompletedPhase 2NCT05047185
Dose-ranging Study of Oral PHA-022121 for Prophylaxis Against Angioedema Attacks in Patients With Hereditary Angioedema Type I or Type II
Studying Hereditary angioedema
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Pharvaris Netherlands B.V.
- Principal Investigator
- Marc Riedl, MDUC San Diego, La Jolla, California, United States
- Intervention
- Deucrictibant low dose(drug)
- Enrollment
- 34 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2022 – 2025
Study locations (19)
- Study site, Birmingham, Alabama, United States
- Study site, Paradise Valley, Arizona, United States
- Study site, St Louis, Missouri, United States
- Study Site, Vienna, Austria
- Study site, Sofia, Bulgaria
- Study site, Ottawa, Ontario, Canada
- Study site, Montreal, Quebec, Canada
- Study site, Berlin, Germany
- Study site, Frankfurt, Germany
- Study site, Dublin, Ireland
- Study site, Padua, PD, Italy
- Study site, Milan, Italy
- Study site, Palermo, Italy
- Study site, Krakow, Poland
- Study site, Brighton, England, United Kingdom
- +4 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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