Clinical trial
Evaluation of Long-term Safety of ADYNOVI/ADYNOVATE (Antihaemophilic Factor [Recombinant] PEGylated, Rurioctocog Alfa Pegol) in Patients With Haemophilia A - An ADYNOVI/ADYNOVATE Post-Authorisation Safety Study (PASS)
NCT04158934 is registered in ClinicalTrials.gov with Baxalta now part of Shire as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Evaluation of Long-term Safety of ADYNOVI/ADYNOVATE (Antihaemophilic Factor [Recombinant] PEGylated, Rurioctocog Alfa Pegol) in Patients With Haemophilia A - An ADYNOVI/ADYNOVATE Post-Authorisation Safety Study (PASS)
- Lead sponsor
- Baxalta now part of Shire
- Phase
- Observational
- Overall status
- Active, not recruiting
- Start date
- July 9, 2020
- Completion date
- February 28, 2030
- Enrollment
- 207 (actual)
- Sites
- 36
Conditions
As the registry lists them; a condition with its own page is linked.