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

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexMale
Age18+
SponsorPfizer

About this trial

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.

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Testing of hepatic AAV Vector integration

Treatment groups

173 Participants
are divided into 2 treatment groups

Locations

23
Australia
Royal Prince Alfred Hospital2050, CamperdownNew South Wales, Australia
Sydney Local Health District (RPAH Zone)2050, CamperdownNew South Wales, Australia
Canada
Unity Health Toronto, St. Michael's HospitalM5B 1W8, TorontoOntario, Canada
South Korea
Kyung Hee University Hospital at Gangdong05278, Seoul South Korea

Sponsors and collaborators

Pfizer

Lead sponsor