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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00816660
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 1
Start date December 1, 2008
Completion date August 31, 2010

See also
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