Prospective Registry of European Hemophilia B Patients Receiving BeneFIX® for Usual Use
A Prospective Registry of European Hemophilia B Patients Receiving BeneFIX®(Nonacog Alfa, Recombinant Human Factor IX) for Usual Use
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
This observational or N/A phase trial investigates Hemophilia B and is currently completed. Wyeth is now a wholly owned subsidiary of Pfizer leads this study, which shows 7 recorded versions since 2002 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
7 versions recorded-
Sep 2025 — Present [monthly]
Completed
-
Sep 2024 — Sep 2025 [monthly]
Completed
-
Jul 2024 — Sep 2024 [monthly]
Completed
-
Jan 2021 — Jul 2024 [monthly]
Completed
-
Jun 2018 — Jan 2021 [monthly]
Completed
▶ Show 2 earlier versions
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Apr 2018 — Jun 2018 [monthly]
Completed
Phase: PHASE4 → None
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Jan 2017 — Apr 2018 [monthly]
Completed PHASE4
First recorded
Jan 2002
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Wyeth is now a wholly owned subsidiary of Pfizer
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
Almería, Spain , Amiens, France , Amsterdam, Netherlands , Ancona, Italy , Angers, France , Barcelona, Spain , Bari, Italy , Birmingham, United Kingdom , Breda, Netherlands , Brussels, Belgium and 69 more locations