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Clinical Trial Summary

Study to evaluate the safety and effectiveness of ReFacto AF for the treatment of severe hemophilia A in patients who have not yet received treatment for their hemophilia. Study subjects will be males less than 6 years old who have not taken any clotting factor or other blood products before the study. The safety and effectiveness of ReFacto AF will be determined in this study by tests and procedures done at the doctor's office.


Clinical Trial Description

Regulatory Commitment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00950170
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 4
Start date February 10, 2010
Completion date November 24, 2016

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