Clinical trial
Study Evaluating rFIX; BeneFIX in Severe Hemophilia B
NCT00037557 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Completed
Key facts
| NCT number | NCT00037557 |
|---|---|
| Title | Study Evaluating rFIX; BeneFIX in Severe Hemophilia B |
| Official title | An Open-Label, Single-Arm, Safety and Efficacy Study of Recombinant Human Factor IX (rFIX; BeneFIX®) in Children Less Than 6 Years of Age With Severe Hemophilia B |
| Lead sponsor | Wyeth is now a wholly owned subsidiary of Pfizer, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Hemophilia B |
| Intervention type | Drug |
| Interventions | BeneFIX |
| Enrollment | 20 |
| Start date | Sep 1, 2002 |
| Completion | Nov 1, 2007 |
| First posted | May 20, 2002 |
| Last update posted | Dec 27, 2007 |
| Countries | United States |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: