CompletedPhase 2NCT00989196
Clinical Study to Investigate the Pharmacokinetics, Efficacy, Safety and Immunogenicity of a Recombinant FVIII in Patients With Severe Hemophilia A
Studying Severe hemophilia A
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
- Octapharma
- Principal Investigator
- Sigurd Knaub, PhDOctapharma
- Intervention
- Human-cl rhFVIII(biological)
- Enrollment
- 22 target
- Eligibility
- 12-65 years · MALE
- Timeline
- 2010 – 2012
Study locations (9)
- UCLA Orthodpedic Hospital, Los Angeles, California, United States
- University of California, Davis, Sacramento, California, United States
- University of Colorado, Denver, Colorado, United States
- Georgetown University, Washington D.C., District of Columbia, United States
- RUSH University Medical Center, Chicago, Illinois, United States
- University of Medicine and Dentistry, New Brunswick, New Jersey, United States
- Prof. Lissitchkov, Sofia, Bulgaria
- Medizinische Hochschule, Hanover, Lower Saxony, Germany
- Vivantes Klinikum, Berlin, Germany
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.
Open NCT00989196 on ClinicalTrials.govOther trials for Severe hemophilia A
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