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Safety and Effectiveness of Giroctocogene Fitelparvovec or Fidanacogene Elaparvovec in Patients With Hemophilia A or B Respectively

RecruitingPhase 3Ages 18 Years - anyMalePfizer
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In plain words

What the trial is, and whether it could suit you

A study to learn about the long-term safety and efficacy of giroctocogene fitelparvovec or fidanacogene elaparvovec in patients with hemophilia A or hemophilia B respectively, who have received treatment through prior participation in a Pfizer-sponsored clinical trial. Data collection and participant visits will be based on standard of care.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: -Only participants who received investigational giroctocogene fitelparvovec or fidanacogene eleparvovec and were enrolled in a Pfizer-sponsored study (C0371002, C0371003, C0371005, C3731001, C3731003) are eligible. Exclusion Criteria: -None
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What it tests

  • Testing of hepatic AAV Vector integration
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Where

39 sites
The Regents of the University of California||UC Davis Health
Rancho Cordova, United States
UC Davis Health
Sacramento, United States
UC Davis Ambulatory Care Clinic
Sacramento, United States
UC Davis Hemophilia Treatment Center
Sacramento, United States
UC Davis Medical Center
Sacramento, United States
UCSF Outpatient Hematology Clinic
San Francisco, United States
USF Health Morsani Center For Advanced Healthcare
Tampa, United States
The University of South Florida Board of Trustees
Tampa, United States

…and 31 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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