CompletedPhase 4NCT00323856
Safety Study of Alphanate in Previously Treated 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
- Grifols Biologicals, LLC
- Principal Investigator
- Michael Ken WoodwardInstituto Grifols SA
- Intervention
- Alphanate SD/HT(drug)
- Enrollment
- 51 enrolled
- Eligibility
- 6-65 years · MALE
- Timeline
- 2003 – 2018
Study locations (2)
- Oddzial Chorob Wewnetrznych i Hematologii, Poznan, Szkolna, Poland
- Katedra i Klinika Hematologii Collegium Medicum UJ, Krakow, Poland
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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