CompletedPHASE2, PHASE3NCT01486927
An Open-label Safety, Efficacy and Pharmacokinetic Study of a Recombinant FVIII Compared to Recombinant Human Antihemophilic FVIII in Patients With Severe Hemophilia A
Studying Hemophilia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- CSL Behring
- Principal Investigator
- Program DirectorCSL Behring
- Intervention
- rVIII-SingleChain(biological)
- Enrollment
- 175 enrolled
- Eligibility
- 12-65 years · MALE
- Timeline
- 2012 – 2014
Study locations (30)
- Study Site, Sacramento, California, United States
- Study Site, San Diego, California, United States
- Study Site, Aurora, Colorado, United States
- Study Site, Hartford, Connecticut, United States
- Study Site, Miami, Florida, United States
- Study Site, Chicago, Illinois, United States
- Study Site, New Orleans, Louisiana, United States
- Study Site, Houston, Texas, United States
- Study Site, Milwaukee, Wisconsin, United States
- Study Site, Nedlands, Australia
- Study Site, Perth, Australia
- Study Site, Graz, Austria
- Study Site, Vienna, Austria
- Study Site, New Brunswick, Canada
- Study Site, Hradec Králové, Czechia
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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