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NCT05662319Active, not recruitingPhase 3

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 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

Source: ClinicalTrials.gov · Last updated 4 Feb 2026

Brief summary (registry, in English)

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

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
91 (actual)
First submitted
14 Dec 2022
Start date
1 Feb 2023
Primary completion date
25 Mar 2027
Lead sponsor
Sanofi
Diseases
Haemophilia
NCT number
NCT05662319
EU CT number
2022-500221-33-01
EudraCT number
2022-500221-33

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 91
  • From 1 Feb 2023 to the primary completion date, 25 Mar 2027
  • 54 sites in 17 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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

Other illness

  • 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).
  • 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

Lab values

  • Known to be HIV positive with CD4 count \<200 cells/μL.

Other

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

Who the study is looking for

  • 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

Age in the registry: 12 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (54)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
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HamiltonCanadaUnknown status
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HamiltonCanadaUnknown status
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TorontoCanadaUnknown status
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BeijingChinaUnknown status
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GuangzhouChinaUnknown status
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JinanChinaUnknown status
Vivantes Netzwerk fuer Gesundheit GmbH
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BerlinGermanyActive, not recruiting
University Medical Center Hamburg-Eppendorf
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HamburgGermanyActive, not recruiting
Complexo Hospitalario Universitario A Coruña
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A CoruñaSpainActive, not recruiting
Hospital Universitario La Paz
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MadridSpainActive, not recruiting
Hospital Unviersitario Miguel Servet
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ZaragozaSpainActive, not recruiting
Assistance Publique Hopitaux De Paris
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Le Kremlin-BicetreFranceActive, not recruiting
Centre Hospitalier Regional Universitaire De Lille
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Lille CedexFranceActive, not recruiting
Assistance Publique Hopitaux de Paris
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ParisFranceActive, not recruiting
Laiko General Hospital of Athens
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AthensGreeceActive, not recruiting
Nosokomeio Paidon I Agia Sofia
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AthensGreeceActive, not recruiting
Ippokratio General Hospital of Thessaloniki
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ThessalonikiGreeceActive, not recruiting
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BangaloreIndiaUnknown status
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BhubaneswarIndiaUnknown status
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Pune-411011IndiaUnknown status
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PunjabIndiaUnknown status
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VelloreIndiaUnknown status
Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico
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MilanItalyActive, not recruiting
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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RomeItalyActive, not recruiting
Humanitas Research Hospital
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RozzanoItalyActive, not recruiting
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Kashihara-shiJapanUnknown status
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NagoyaJapanUnknown status
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Saitama-shiJapanUnknown status
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SeoulSouth KoreaUnknown status
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SeoulSouth KoreaUnknown status
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Chihuahua CityMexicoUnknown status
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MonterreyMexicoUnknown status
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VeracruzMexicoUnknown status
Samodzielny Publiczny Zaklad Opieki Zdrowotnej Szpital Uniwersytecki w Krakowie
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KrakowPolandActive, not recruiting
Wojewodzkie Wielospecjalistyczne Centrum Onkologii i Traumatologii im. M. Kopernika w Lodzi
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LodzPolandActive, not recruiting
Instytut Hematologii I Transfuzjologii
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WarsawPolandActive, not recruiting
Uniwersyteckie Centrum Kliniczne Warszawskiego Uniwersytetu Medycznego
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WarsawPolandActive, not recruiting
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JeddahSaudi ArabiaUnknown status
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TaipeiTaiwanUnknown status
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TaipeiTaiwanUnknown status
University Hospitals of Cleveland Site Number : 8400001
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ClevelandUnited StatesUnknown status
Children's Medical Center Dallas- Site Number : 8400018
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DallasUnited StatesUnknown status
Hackensack University Site Number : 8400009
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HackensackUnited StatesUnknown status
Gulf States Hemophilia and Thrombophilia Center- Site Number : 8400002
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HoustonUnited StatesUnknown status
M Health Fairview University of Minnesota Medical Center - West Bank- Site Number : 8400016
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MinneapolisUnited StatesUnknown status
Northwell Health Hemostasis and Thrombosis Center Site Number : 8400015
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New Hyde ParkUnited StatesUnknown status
Center for Inherited Blood Disorders (CIBD) Site Number : 8400012
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OrangeUnited StatesUnknown status
UPMC Children's Hospital of Pittsburgh-4401 Penn Ave Site Number : 8400017
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PittsburghUnited StatesUnknown status
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JohannesburgSouth AfricaUnknown status
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ParktownSouth AfricaUnknown status
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AdanaTurkey (Türkiye)Unknown status
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AkdenizTurkey (Türkiye)Unknown status
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ÇapaTurkey (Türkiye)Unknown status
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IzmirTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.