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A study to test a medicine (fitusiran) injected under the skin for preventing bleeding episodes in male adolescent or adult participants with severe Hemophilia

Phase 1
Recruiting
Conditions
Hemophilia
MedDRA version: 20.0Level: LLTClassification code: 10066439Term: Hemophilia Class: 10010331
Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Registration Number
CTIS2022-500221-33-01
Lead Sponsor
Sanofi-Aventis Research & Development
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
75
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 requirements

Exclusion Criteria

Known co-existing bleeding disorders other than congenital hemophilia A or B, AT activity <60% at Screening, Co-existing thrombophilic disorder, Hepatitis C virus antibody positive, except participants who have negative Hepatitis C viral load and no evidence of cirrhosis, Presence of acute hepatitis, ie, hepatitis A, hepatitis E., Presence of acute or chronic hepatitis B infection, Known to be HIV positive with CD4 count <200 cells/µL., Reduced renal function, History of arterial or venous thromboembolism, not associated with an indwelling venous access, History of intolerance to SC injection(s)., Current participation in immune tolerance induction therapy (ITI), Prior gene therapy, Current or prior participation in a fitusiran trial, Current or prior participation in a gene therapy trial, Received 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 longer, Presence of clinically significant liver disease

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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