RecruitingNCT06883240
An Observational Study of Participants With Type 3 Von Willebrand Disease on Prophylactic Standard-of-Care Treatment
Studying Von Willebrand disease
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Hoffmann-La Roche
- Principal Investigator
- Clinical TrialsHoffmann-La Roche
- Intervention
- Von Willebrand Factor Concentrates(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 2 years · All sexes
- Timeline
- 2025 – 2026
Study locations (27)
- UC Davis, Sacramento, California, United States
- University of Florida, Gainesville, Florida, United States
- University of Minnesota Medical Center, Minneapolis, Minnesota, United States
- Washington University School of Medicine, St Louis, Missouri, United States
- UZ Leuven Gasthuisberg, Leuven, Belgium
- The Hospital for Sick Children, Toronto, Ontario, Canada
- McGill University Health Center, Montreal, Quebec, Canada
- IPS SURA Industriales Medellín, Medellín, Colombia
- Hopital Claude Huriez - CHU Lille, Lille, France
- Groupe Hospitalier Necker Enfants Malades, Paris, France
- Universitätsklinikum Bonn, Bonn, Germany
- Gerinnungszentrum Rhein-Ruhr;Gerinnungsambulanz, Duisburg, Germany
- Hämophiliezentrum Med. Klinik III/Institut für Transfusionsmedizin, Frankfurt/M., Germany
- Universita' Degli Studi La Sapienza-Ist.Di Ematologia, Rome, Lazio, Italy
- IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Lombardy, Italy
- +12 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.
Open NCT06883240 on ClinicalTrials.govOther trials for Von Willebrand disease
Additional recruiting or active studies for the same condition.
- RECRUITINGNCT07404644An Observational Study of Vonicog Alfa (rVWF) in Pediatric Participants With Von Willebrand Disease (vWD)Takeda
- RECRUITINGPHASE3NCT07115004Study to Evaluate Subcutaneous (SC) VGA039 in Patients With Von Willebrand Disease (VWD)Vega Therapeutics, Inc
- RECRUITINGPHASE3NCT07129343A Study of Recombinant Von Willebrand Factor (rVWF) in Chinese Participants With Von Willebrand Disease (vWD)Takeda
- RECRUITINGPHASE3NCT06998524A Study to Assess the Efficacy and Safety of Emicizumab in Participants With Type 3 Von Willebrand DiseaseHoffmann-La Roche
- RECRUITINGPHASE3NCT05582993A Study of Vonicog Alfa (rVWF) in Children With Severe Von Willebrand Disease (vWD)Takeda
- RECRUITINGPHASE3NCT06205095A Pilot Crossover Trial of Prophylactic Wilate Compared to Placebo for Heavy Menstrual Bleeding in Patients with VWDUnity Health Toronto
- RECRUITINGPHASE1, PHASE2NCT05776069Study of VGA039 in Healthy Volunteers and Patients With Von Willebrand Disease (VIVID)Vega Therapeutics, Inc
- ACTIVE NOT RECRUITINGNCT03853486ATHN 9: Severe VWD Natural History StudyAmerican Thrombosis and Hemostasis Network