Clinical trial
A Postauthorization Safety Surveillance Study Of Patients Switching To ReFacto AF From ReFacto Or Other Factor VIII Products In Usual Care Settings
NCT00884390 is registered in ClinicalTrials.gov with Pfizer as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Postauthorization Safety Surveillance Study Of Patients Switching To ReFacto AF From ReFacto Or Other Factor VIII Products In Usual Care Settings
- Lead sponsor
- Pfizer
- Phase
- Phase 4
- Overall status
- Terminated
- Start date
- May 31, 2009
- Completion date
- March 31, 2013
- Enrollment
- 208 (actual)
- Sites
- 74
Conditions
As the registry lists them; a condition with its own page is linked.