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An Observational Study of Vonicog Alfa (rVWF) in Pediatric Participants With Von Willebrand Disease (vWD)
Sponsor: Takeda
Summary
This study is conducted in Japan of vonicog alfa (rVWF) used to treat pediatric participants with Von Willebrand Disease (vWD). The main aim of the study is to evaluate adverse drug reaction and effectiveness of vonicog alfa (rVWF). During the study, pediatric participants with vWD will be administered with rVWF under routine normal practice. The investigators will evaluate adverse events due to rVWF for 1 year from the start of drug administration. The study sponsor will not be involved in how the participants are administered but will be recorded what happens during the study.
Official title: Vonvendi Intravenous Specified Drug Use-results Survey "Pediatric Administration"
Key Details
Gender
All
Age Range
Any - 17 Years
Study Type
OBSERVATIONAL
Enrollment
13
Start Date
2026-02-19
Completion Date
2031-05-30
Last Updated
2026-02-23
Healthy Volunteers
No
Conditions
Interventions
vonicog alfa (rVWF)
rVWF administered by intravenous injection.
Locations (1)
Takeda selected site
Tokyo, Tokyo, Japan