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Phase 2 N=15 Treatment

Gene Therapy Study in Severe Haemophilia A Patients (270-201)

Severe Haemophilia A

Enrolled (actual)
15
Serious AEs
60.0%
Results posted
Apr 2025
Primary outcome: Primary: Number of Participants With Treatment Emergent Adverse Events — 1; 1; 6; 7 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
valoctocogene roxaparvovec (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
Male
Sponsor
BioMarin Pharmaceutical
Primary completion
Feb 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Treatment Emergent Adverse Events
1; 1; 6; 7; 1; 0
PRIMARY
Number of Participant With Median FVIII Activity Levels >= 5 IU/dL Using Chromogenic Substrate Assay (CSA)
0; 0; 5; 7
PRIMARY
Median FVIII Activity as Measured by Chromogenic Substrate Assay During Week 13-16 Post-BMN 270 Infusion
0.00; 0.00; 16.30; 50.40
SECONDARY
Annualized Bleeding Rate Requiring Exogenous Factor VIII Replacement Treatment During Week 5 and Beyond
1.87; 6.20; 1.58; 0.75
SECONDARY
Annualized Factor VIII Utilization During Week 5 and Beyond
2536.47; 279.27; 331.65; 228.72
SECONDARY
Annualized Factor VIII Infusion Rate During Week 5 and Beyond
77.98; 10.09; 10.25; 6.38

Summary

This study is being conducted by BioMarin Pharmaceutical Inc. as an open label, dose escalation study in order to determine the safety and efficacy of valoctocogene roxaparvovec (an Adenovirus-Associated Virus based gene therapy vector in participants with severe haemophilia A.

Eligibility Criteria

Inclusion Criteria

  • Males 18 years or older with established severe Haemophilia A (endogenous FVIII level ≤1 IU/dL) as evidenced by their medical history.
  • Treated/exposed to FVIII concentrates or cryoprecipitate for a minimum of 150 exposure days (EDs)
  • Greater than or equal to 12 bleeding episodes for patients on on-demand FVIII replacement therapy over the previous 12 months. Does not apply to patients on prophylaxis
  • No history of inhibitor, and results from a modified Nijmegen Bethesda assay of less than 0.6 Bethesda Units (BU) 2 consecutive occasions at least one week apart within the past 12 months
  • Sexually active patients must be willing to use an acceptable method of contraception.

Exclusion Criteria

  • Detectable pre-existing immunity to the AAV5 capsid as measured by adeno-associated virus 5 (AAV5) transduction inhibition (TI) or AAV5 total antibodies
  • Any evidence of immunosuppressive disorder or active chronic infection including hepatis B, hepatitis C, HIV
  • Significant liver dysfunction as defined by abnormal elevation ofliver function tests, or for patients who have undergone liver imaging or biopsy and found to have evidence of grade 3 or higher fibrosis
  • Evidence of any bleeding disorder not related to haemophilia A
  • 12. Treatment with any investigational product within 30 days prior to the end of the screening period, or any previous exposure to any gene transfer therapy
  • Any disease or condition that per the physician's discretion would prevent the patient from fully complying with the requirements of the study including possible corticosteroid treatment outlined in the protocol. The physician may exclude patients unwilling or unable to agree on not using alcohol for the 16-week period following the viral infusion.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02576795). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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