Gene Therapy Study in Severe Hemophilia A Patients With Antibodies Against AAV5
Reason given: Early rollover into long-term extension study
Key facts
- Where
- Kaohsiung City, Taichung, and Taipei, TaiwanSee the 4 sites
- Phase
- Phase 1/2
Where in Taiwan
- Kaohsiung Medical University Chung-Ho Memorial HospitalKaohsiung City, TaiwanNo longer taking part
- Taichung Veterans General HospitalTaichung, TaiwanNo longer taking part
- National Taiwan University HospitalTaipei, TaiwanNo longer taking part
- Tri-Service General HospitalTaipei, TaiwanNo longer taking part
Trial details
- Who runs it
- BioMarin Pharmaceutical
- Trial code
- NCT03520712
- Record updated
- 22 August 2025
- Original description
This study is being conducted by BioMarin Pharmaceutical Inc. as an open label, single dose study to determine the safety of valoctocogene roxaparvovec (an Adenovirus-Associated Virus (AAV) based gene therapy vector) in severe Hemophilia A patients with pre-existing antibodies against AAV5.Read full original descriptionShow less
A Phase 1/2 Safety, Tolerability, and Efficacy Study of Valoctocogene Roxaparvovec, an Adeno-Associated Virus Vector-Mediated Gene Transfer of Human Factor VIII in Hemophilia A Patients With Residual FVIII Levels ≤ 1 IU/dL and Pre-existing Antibodies Against AAV5
This study is being conducted by BioMarin Pharmaceutical Inc. as an open label, single dose study to determine the safety of valoctocogene roxaparvovec (an Adenovirus-Associated Virus (AAV) based gene therapy vector) in severe Hemophilia A patients with pre-existing antibodies against AAV5.
Inclusion: Males ≥ 18 years of age with hemophilia A and residual FVIII levels ≤ 1 IU/dL as evidenced by medical history, at the time of signing the informed consent; Detectable pre-existing antibodies against the AAV5 vector capsid as measured by AAV5 total antibody ELISA; Subject must have been on prophylactic FVIII replacement therapy for at least 12 months prior to study entry; No previous documented history of a detectable FVIII inhibitor, and results from a Bethesda assay or Bethesda assay with Nijmegen modification of less than 0.6 Bethesda Units (BU) (or less than 1.0 BU for laboratories with a historical lower sensitivity cutoff for inhibitor detection of 1.0 BU) on 2 consecutive occasions at least one week apart within the past 12 months (at least one of which should be tested at the central laboratory); Sexually active participants must agree to use an acceptable method of effective contraception. Participants must agree to contraception use for at least 12 weeks post-infusion.
Exclusion: Evidence of liver dysfunction as assessed by liver tests and most recent, prior FibroScan or liver biopsy showing significant fibrosis of 3 or 4 as rated on a scale of 0-4 on the Batts-Ludwig (Batts 1995) or METAVIR (Bedossa 1996) scoring systems, or an equivalent grade of fibrosis if an alternative scale is used; Chronic or active hepatitis B or C as evidenced by testing at screening; Active malignancy, except non-melanoma skin cancer, or history of hepatic malignancy; Any condition that, in the opinion of the investigator or Sponsor would prevent the patient from fully complying with the requirements of the study (including corticosteroid treatment and/or use of alternative immunosuppressive agents outlined in the protocol) and/or would impact or interfere with evaluation and interpretation of subject safety or efficacy result; Any evidence of active infection including COVID-19, or any immunosuppressive disorder, except for HIV infection. HIV positive patients who meet all other eligibility criteria may be included if they have a CD4 count > 200/mm3 and an undetectable viral load (unquantifiable viral load as defined as less than the limit of quantification by the testing laboratory's assay is permitted) while receiving an antiretroviral therapy (ART) regimen that does not contain efavirenz or another potentially hepatotoxic ART.