Active, not recruitingPHASE1, PHASE2NCT05406362
Assess Safety and Efficacy of VAD044 in HHT Patients
Studying Hereditary hemorrhagic telangiectasia
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
- Vaderis Therapeutics AG
- Principal Investigator
- Damien PicardVaderis Therapeutics AG
- Intervention
- VAD044 Part I(drug)
- Enrollment
- 75 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2027
Study locations (7)
- Massachusetts General Hospital, Boston, Massachusetts, United States
- Universitair Ziekenhuis Gent, Ghent, Belgium
- Hospices Civils de Lyon, Lyon, France
- Ospedale Maggiore di Crema, Crema, Italy
- St. Antonius Hospital, Nieuwegein, Netherlands
- Hospital Universiati De Bellvitge, Barcelona, Spain
- Hospital Universitario Ramón y Cajal, Madrid, Spain
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.
Open NCT05406362 on ClinicalTrials.govOther trials for Hereditary hemorrhagic telangiectasia
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