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 3Active Not RecruitingNCT05662319

Sanofi91 enrolled

Overview

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

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Hemophilia

Interventions

Eligibility

Sex: MALEMin age: 12 Years

Medical Language ↔ Plain English

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 * 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 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 The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Outcomes

Primary Outcomes

Annualized bleeding rate (ABR) in the fitusiran primary efficacy period

A bleeding episode is defined as any occurrence of hemorrhage that requires administration of CFCs or BPAs, e.g., hemarthrosis, muscle, or mucosal bleeding.

Time frame: Day 169 to Day 505 (since the first dose of fitusiran)

Secondary Outcomes

Annualized bleeding rate (ABR) while on fitusiran prophylaxis in the fitusiran primary efficacy period and ABR while on prophylaxis standard of care (SOC) in the SOC period

A bleeding episode is defined as any occurrence of hemorrhage that requires administration of CFCs or BPAs, e.g., hemarthrosis, muscle, or mucosal bleeding.

Time frame: Day 169 to Day 505 (primary efficacy period) and Day -168 to Day -1 (SOC period)

Annualized bleeding rate (ABR) while on fitusiran prophylaxis in the fitusiran primary efficacy period and ABR while on on-demand standard of care (SOC) in the SOC period

A bleeding episode is defined as any occurrence of hemorrhage that requires administration of CFCs or BPAs, e.g., hemarthrosis, muscle, or mucosal bleeding.

Time frame: Day 169 to Day 505 (primary efficacy period) and Day -168 to Day -1 (SOC period)

Annualized spontaneous bleeding rate in the fitusiran primary efficacy period and in the SOC period

A bleeding episode is defined as any occurrence of hemorrhage that requires administration of CFCs or BPAs, e.g., hemarthrosis, muscle, or mucosal bleeding. A spontaneous bleeding episode is a bleeding event that occurs for no apparent or known reason, particularly into the joints, muscles, and soft tissues.

Time frame: Day 169 to Day 505 (primary efficacy period) and Day -168 to Day -1 (SOC period)

Annualized joint bleeding rate in the fitusiran primary efficacy period and in the SOC period

A bleeding episode is defined as any occurrence of hemorrhage that requires administration of CFCs or BPAs, e.g., hemarthrosis, muscle, or mucosal bleeding. A joint bleeding episode is characterized by an unusual sensation in the joint ("aura") in combination with 1) increasing swelling or warmth over the skin over the joint, 2) increasing pain, or 3) progressive loss of range of motion or difficulty in using the limb as compared with baseline.

Time frame: Day 169 to Day 505 (primary efficacy period) and Day -168 to Day -1 (SOC period)

Change in Haem-A-QOL physical health score and total score during SOC and during fitusiran prophylaxis

The Haem-A-QoL will be provided to participants ≥17 years of age and includes 46 items contributing to 10 QoL domains (physical health, feelings, view of yourself, sports and leisure, work and school, dealing with hemophilia, treatment, future, family planning, partnership, and sexuality). Scoring for each item is based on a 5-point Likert scale (never, rarely, sometimes, often, and all the time), and higher scores represent greater impairment.

Time frame: Day 1 (D1) to Day 505, and from D1 to Day 1009, and during SOC from Day-168 to D-1

Annualized bleeding rate (ABR) in the fitusiran 18-month efficacy period

A bleeding episode is defined as any occurrence of hemorrhage that requires administration of CFCs or BPAs, e.g., hemarthrosis, muscle, or mucosal bleeding.

Time frame: Day 1 to Day 505

Annualized bleeding rate (ABR) in the fitusiran 36-month treatment period

A bleeding episode is defined as any occurrence of hemorrhage that requires administration of CFCs or BPAs, e.g., hemarthrosis, muscle, or mucosal bleeding.

Time frame: Day 1 to Day 1009

Annualized weight-adjusted consumption of CFC/BPA

All CFC or BPA doses (including doses per kg body weight) administered during the study treatment will be recorded

Time frame: Day -168 until Day 1009

Number of participants with adverse events

All AEs (serious or nonserious) will be collected from the signing of the informed consent form (ICF) until last AT follow up visit.

Time frame: Date of signed ICF (Day -228 to Day -169) until last visit (approximately 50 months after date of signed ICF)

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

Overview

Conditions

Interventions

Eligibility

Locations (50)

Outcomes

Primary Outcomes

Secondary Outcomes