Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT07404644

An Observational Study of Vonicog Alfa (rVWF) in Pediatric Participants With Von Willebrand Disease (vWD)

Sponsor: Takeda

View on ClinicalTrials.gov

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

Interventions

DRUG

vonicog alfa (rVWF)

rVWF administered by intravenous injection.

Locations (1)

Takeda selected site

Tokyo, Tokyo, Japan