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Recruiting Phase 3 NCT05568719

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

Phase 3 – large-scale trial before approval
Conditions: Hemophilia A Hemophilia B

Sponsor: Pfizer

trial.available_in: БГ
Overview
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.
Who can participate
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
Locations 4
Australia (1)
Royal Prince Alfred Hospital
Camperdown , New South Wales
Taiwan (1)
National Taiwan University Hospital
Taipei
NOT_YET_RECRUITING
Turkey (1)
Ege Universitesi Hastanesi
Izmir , İ̇zmir
United States (1)
The Regents of the University of California||UC Davis Health
Rancho Cordova , California
Technical details
Status
Recruiting
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male only
Minimum age
18 Years
Healthy volunteers
No
Start date
28.12.2022
Completion date
25.02.2040
Registry ID
NCT05568719
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.