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Long-term Safety and Efficacy Study of Fitusiran in Patients With Hemophilia A or B With or Without Inhibitory Antibodies to Factor VIII or IX

Long-term Safety and Efficacy Study of Fitusiran in Patients With Hemophilia A or B With or Without Inhibitory Antibodies to Factor VIII or IX

Recruiting
12 years and older
Male
Phase 3
  • Simplified description (AI rewritten)
  • Technical description (Original)

The estimated total time on study for each participant is up to 55 months which consists of a screening period of up to 30 days, an open label treatment period of up to 48 months and a follow up period of up to 6-month after the last dose of fitusiran

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Study details
    Hemophilia A
    hemophilia
    hemophilia

NCT03754790

Genzyme, a Sanofi Company

19 February 2024

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