A PHASE 3, NON-INVESTIGATIONAL PRODUCT, MULTI COUNTRY COHORT STUDY TO DESCRIBE THE LONG-TERM SAFETY AND EFFECTIVENESS OF A PRIOR SINGLE-DOSE TREATMENT WITH INVESTIGATIVE GIROCTOCOGENE FITELPARVOVEC OR FIDANACOGENE ELAPARVOVEC IN PARTICIPANTS WITH HEMOPHILIA A OR HEMOPHILIA B, RESPECTIVELY
Latest Information Update: 16 Apr 2025
At a glance
- Drugs Fidanacogene-elaparvovec (Primary) ; Giroctocogene fitelparvovec (Primary)
- Indications Haemophilia A; Haemophilia B
- Focus Adverse reactions; Registrational; Therapeutic Use
- Sponsors Pfizer
Most Recent Events
- 11 Apr 2025 Planned End Date changed from 3 Sep 2039 to 25 Feb 2040.
- 11 Apr 2025 Planned primary completion date changed from 3 Sep 2039 to 25 Feb 2040.
- 19 Jul 2024 Planned End Date changed from 8 Apr 2038 to 3 Sep 2039.