RecruitingNCT07404644
An Observational Study of Vonicog Alfa (rVWF) in Pediatric Participants With Von Willebrand Disease (vWD)
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
- Takeda
- Principal Investigator
- Study DirectorTakeda
- Intervention
- vonicog alfa (rVWF)(drug)
- Enrollment
- 13 target
- Eligibility
- 17 years · All sexes
- Timeline
- 2026 – 2031
Study locations (1)
- Takeda selected site, Tokyo, Tokyo, Japan
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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