A Study to Test a Medicine (Fitusiran) for Preventing Bleeds in People With Severe Hemophilia Who Previously Received Preventive Treatment With Emicizumab

PHASE4RecruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

March 1, 2024

Primary Completion Date

September 19, 2026

Study Completion Date

November 30, 2029

Conditions
Hemophilia A
Interventions
DRUG

Fitusiran (SAR439774)

Pharmaceutical form:Solution for injection-Route of administration:Subcutaneous (SC) injection

BIOLOGICAL

Clotting factor concentrates (CFC) or bypassing agents (BPA)

Pharmaceutical form: Solution for injection-Route of administration: Intravenous (IV) injection

BIOLOGICAL

Antithrombin concentrate (ATIIIC)

Pharmaceutical form:Solution for injection-Route of administration:Intravenous (IV) injection

BIOLOGICAL

Emicizumab

Pharmaceutical form:Solution for injection-Route of administration:SC injection

Trial Locations (2)

10041

RECRUITING

Investigational Site Number : 1580001, Taipei

90027

RECRUITING

Children's Hospital Los Angeles- Site Number : 8400005, Los Angeles

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY

NCT06145373 - A Study to Test a Medicine (Fitusiran) for Preventing Bleeds in People With Severe Hemophilia Who Previously Received Preventive Treatment With Emicizumab | Biotech Hunter | Biotech Hunter