ALN-AT3SC-003: ATLAS INH: A Phase 3 Study to Evaluate the Efficacy and Safety of Fitusiran in Patients with Hemophilia A or B with Inhibitory Antibodies to Factor VIII or IX

Brief description of study

This study will evaluate the efficacy and safety of fitusiran compared to on-demand treatment with bypassing agents, as determined by the frequency of bleeding episodes in enrolled adult subjects who are who have hemophilia A or B with an inhibitor who are not on prophylaxis.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Hemophilia
  • Age: - 99 Years
  • Gender: All
Updated on 29 Jan 2020. Study ID: 830125

Interested in the study

Select a study center that’s convenient for you, and get in touch with the study team.

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