rVWF IN PROPHYLAXIS

Status Completed

Clinical Trial Summary

The purpose of this phase 3 study is to investigate the efficacy and safety, including immunogenicity, thrombogenicity and hypersensitivity reactions, as well as pharmacokinetics (PK), health related quality of life (HRQoL) and pharmacoeconomics of prophylactic treatment with recombinant von Willebrand factor (rVWF) (vonicog alfa) in adult participants with severe von Willebrand disease (VWD).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02973087
Study type	Interventional
Source	Takeda
Contact
Status	Completed
Phase	Phase 3
Start date	November 16, 2017
Completion date	July 6, 2020

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See also
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