A Study With OPTIVATE® in People With Von Willebrand Disease

Status Terminated

Clinical Trial Summary

The main objective of the study is to assess the pharmacokinetics of OPTIVATE® after a single dose of 80 IU/kg VWF:RCo. The secondary objectives of the study are to assess efficacy and safety of OPTIVATE® in long-term use over at least 12 months.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00387192
Study type	Interventional
Source	Bio Products Laboratory
Contact
Status	Terminated
Phase	Phase 3
Start date	November 2006
Completion date	September 2008

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See also
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