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Clinical Trial Summary

The main aim of the study is to check effectiveness, side effects, and tolerability of recombinant von Willebrand Factor (rVWF), with or without ADVATE, in the treatment and control of nonsurgical bleeding events in pediatric participants (less than (<)18 years of age) with severe hereditary von Willebrand disease (VWD). The participants will be treated with rVWF for 12-18 months. Their von Willebrand Disease will be treated by their doctor according to their doctor's usual clinical practice. During the study, participants will be followed up at clinics or over telephone calls.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02932618
Study type Interventional
Source Takeda
Contact Takeda Contact
Phone 1-877-825-3327
Email medinfoUS@takeda.com
Status Recruiting
Phase Phase 3
Start date December 18, 2017
Completion date January 1, 2025

See also
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