This study is in progress, not accepting new patients

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

a study on Hemophilia

Summary

Eligibility
for males ages 12 years and up (full criteria)
Location
at UCSD
Dates
study started
completion around

Description

Summary

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

Official Title

A Phase 3, Single-arm, Multicenter, Multinational, Open-label, One-way Crossover Study to Investigate the Efficacy and Safety of Fitusiran Prophylaxis in Male Participants Aged ≥ 12 Years With Severe Hemophilia A or B With or Without Inhibitory Antibodies to Factor VIII or IX

Keywords

Hemophilia, Hemophilia A, Antithrombins, Antithrombin III, Fitusiran, Clotting factor concentrates (CFC) or bypassing agents (BPA), Antithrombin concentrate (ATIIIC)

Eligibility

You can join if…

Open to males ages 12 years and up

  • 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

You CAN'T join if...

  • 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.

Locations

  • University of California San Diego Site Number : 8400011
    San Diego California 92121 United States
  • Center for Inherited Blood Disorders (CIBD) Site Number : 8400012
    Orange California 92868-4306 United States

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Sanofi
ID
NCT05662319
Phase
Phase 3 Hemophilia Research Study
Study Type
Interventional
Participants
About 79 people participating
Last Updated