RecruitingPhase 4NCT02472665
Efficacy and Safety of Fanhdi®, a High-purity Von Willebrand Containing FVIII Concentrate, in Pediatric Patients With Von Willebrand Disease
Studying Von Willebrand disease
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
- Grifols Therapeutics LLC
- Intervention
- plasma-derived FVIII/VWF concentrate(drug)
- Enrollment
- 8 target
- Eligibility
- 6 years · All sexes
- Timeline
- 2013 – 2026
Study locations (4)
- Hospital Sant Joan de Déu Barcelona, Esplugues de Llobregat, Barcelona, Spain
- Hospital Universitario La Paz, Madrid, Spain
- Hospital Universitario Virgen del Rocío, Seville, Spain
- Hospital Universitario Miguel Servet, Zaragoza, Spain
Collaborators
Instituto Grifols, S.A.
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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