drugset / Trial / NCT00816660

Pharmacokinetic, Safety and Tolerability Study of Recombinant Von Willebrand Factor / Recombinant Factor VIII Complex in Type 3 Von Willebrand Disease

NCT00816660 ↗

Phase 1 Completed 32 enrolled Baxalta now part of Shire
RandomizedCrossoverSingle-blindOther

Summary

The objectives of this study are to evaluate the immediate tolerability and safety of rVWF:rFVIII in subjects with Type 3 Von Willebrand Disease after administration of various dosages of VWF:RCo.

Timeline

Start
2008-12-01
Primary completion
2010-08-31
Completion
2010-08-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Marketed plasma-derived VWF/FVIII concentrate Protein / enzyme biologic — —
Subject rVWF:rFVIII Protein / enzyme biologic — —