drugset / Trial / NCT02250508

A Study to Compare the Pharmacokinetics and Safety of Optivate® and Haemate P® in Patients With Von Willebrand Disease.

NCT02250508

Phase 2 Completed Bio Products Laboratory
Treatment

Summary

The main objectives of the study were * to compare the pharmacokinetics (PK) of Optivate® and Haemate P® in various types of vonWillebrand disease (VWD) using the results from the VWF: RCo, VWF:Ag, VWF:CBA and Factor VIII assays. * to compare the clinical tolerance and safety of these two treatments after single IV infusions in subjects with VWD.

Timeline

Start
2004-12
Primary completion
2005-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Wilate Protein / enzyme biologic Intravenous