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Clinical Trial Summary

1. To compare the efficacy and safety of pharmacokinetic (PK)-guided treatment with BAX 855 targeting FVIII trough levels of 1-3% and approximately 10% (8-12%) 2. To further characterize pharmacokinetic (PK) and pharmacodynamic (PD) parameters of BAX 855


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02585960
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 3
Start date November 23, 2015
Completion date August 5, 2018

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