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Hemophilia A - 41 Studies Found
Estado | Estudiar |
Recruiting |
Nombre del estudio: Post-Marketing Non-Interventional Safety Evaluation of Obizur in the Treatment of Bleeding Episodes for Patients With Acquired Hemophilia A Condición: Acquired Hemophilia A Fecha: 2015-10-29 Intervenciones: Biological: OBIZUR Treating physician will determine treatment regimen, frequency of laboratory and clin |
No longer available |
Nombre del estudio: Expanded Access to B-Domain Deleted Recombinant Porcine Factor VIII (OBI-1) in the Treatment of Acquired Hemophilia A Due to Factor VIII Inhibitory Auto-antibodies Condición: Acquired Hemophilia A Fecha: 2013-10-21 Intervenciones: Biological: OBI-1 Other Name: B-Domain Deleted Recombinant Porcine Factor VIII |
Terminated |
Nombre del estudio: Trial of Rituximab Versus Oral Cyclophosphamide to Eradicate or Suppress Autoimmune Anti-Factor VIII Antibodies in Acquired Hemophilia A Condición: Hemophilia A Fecha: 2006-03-23 Intervenciones:
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Completed |
Nombre del estudio: Study of Modified Recombinant Factor VIII (OBI-1) in Subjects With Acquired Hemophilia A Condición: Hemophilia A Fecha: 2010-08-06 Intervenciones: Biological: OBI-1 Intravenous infusion |
Completed |
Nombre del estudio: Inhibitor Development in Patients With Hemophilia A Undergoing Surgery Condición: Hemophilia A Fecha: 2012-04-04 |
Completed |
Nombre del estudio: Study of a pd vWF/FVIII, Biostate®, in Subjects With Haemophilia A Condición: Hemophilia A Fecha: 2009-04-09 Intervenciones:
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Completed |
Nombre del estudio: Study Evaluating ReFacto® in Hemophilia A Undergoing Major Surgery Condición: Hemophilia A Fecha: 2004-09-28 Intervenciones: Drug: ReFacto |
Completed |
Nombre del estudio: Study Comparing Blood Levels of ReFacto and Advante in Hemophilia A Condición: Hemophilia A Fecha: 2005-09-11 Intervenciones:
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Completed |
Nombre del estudio: Study Evaluating Safety And Efficacy Of Moroctocog Alfa (AF-CC) In Previously Treated Hemophilia A Patients Condición: Hemophilia A Fecha: 2009-06-04 Intervenciones:
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Recruiting |
Nombre del estudio: Multicentre, Non-controlled, Prospective, Post-Marketing Safety Study Following Long-Term Prophylactic OptivateTreatment in Subjects With Severe Haemophilia A Condición: Haemophilia A Fecha: 2013-03-13 Intervenciones: Biological: Optivate 500IU |