drugset / Trial / NCT03154437

An Expanded Access Program of Emicizumab in Participants With Hemophilia A With Inhibitors

NCT03154437 ↗

Expanded access Approved for marketing Genentech, Inc.

Summary

This open-label, multicenter expanded access program (EAP) is designed to provide emicizumab to eligible participants with hemophilia A with factor VIII (FVIII) inhibitors before it is commercially available in the United States for the indication of hemophilia A with FVIII inhibitors. Discontinuation may occur earlier if participant or physician decides to discontinue treatment or the sponsor discontinues emicizumab clinical development.

Timeline

Start
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Primary completion
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Completion
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Drugs

EvaluationDrugModalityDoseRoute
Subject Emicizumab Monoclonal antibody 1.5 mg/kg Subcutaneous

Indications