A Study to Test a Medicine (Fitusiran) Injected Under the Skin for Preventing Bleeding Episodes in Male Adolescent or Adult Participants With Severe Hemophilia

This is a multicenter, multinational, open-label, one-way cross-over, Phase 3, single-arm study for treatment of hemophilia.The purpose of this study is to measure the frequency of treated bleeding episodes with fitusiran in male adult and adolescent (≥12 years old) participants with hemophilia A or B, with or without inhibitory antibodies to factor VIII or IX who have switched from their prior standard of care treatment.The total study duration will be up to approximately 50 months (200 weeks, 1 study month is equivalent to 4 weeks) and will include:A screening period up to approximately 60 days,A standard of care (SOC) period of approximately 6 study months (24 weeks),A fitusiran treatment period of approximately 36 study months (144 weeks),An antithrombin (AT) follow-up period of approximately 6 study months (24 weeks) but may be shorter or longer depending on individual participants AT recovery.The frequency for telephone visits will be approximately every 2 weeks. For site visits the frequency will be approximately every 8 weeks during the SOC period and approximately every 4 weeks during the fitusiran treatment period. If applicable and if allowed by local regulation, home and/or remote visits may be conducted during the study

Inclusion Criteria:Diagnosis of severe congenital hemophilia A or B (FVIII <1% or FIX level ≤2%) as evidenced by a central laboratory measurement at screening or documented medical record evidence.For participants currently not on prophylaxis (CFC or BPA on-demand): A minimum of 4 bleeding episodes requiring BPA (inhibitor participants) or CFC (non-inhibitor participants) treatment within the last 6 months prior to screening.Willing and able to comply with the study requirements and to provide written informed consent and assent in the case of participants under the age of legal consent, per local and national requirementsExclusion Criteria:Known co-existing bleeding disorders other than congenital hemophilia A or BHistory of arterial or venous thromboembolism, not associated with an indwelling venous accessHistory of intolerance to SC injection(s).Current participation in immune tolerance induction therapy (ITI)Prior gene therapyCurrent or prior participation in a fitusiran trialCurrent or prior participation in a gene therapy trialReceived an investigational drug or device within 30 days prior to the screening visit or within 5 half-lives of the investigational drug (or device) prior to the screening visit, whichever is longerPresence of clinically significant liver disease AT activity <60% at ScreeningCo-existing thrombophilic disorderHepatitis C virus antibody positive, except participants who have negative Hepatitis C viral load and no evidence of cirrhosisPresence of acute hepatitis, ie, hepatitis A, hepatitis E.Presence of acute or chronic hepatitis B infectionKnown to be HIV positive with CD4 count <200 cells/μL.Reduced renal function The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.