Post-marketing Surveillance (Use Result Surveillance) With Refixia®
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Phase
—
Status
Completed
Study type
Observational
Enrollment
28actual
Sites
23
Countries
Denmark, Japan
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2019-08-23 | actual | When the study began enrolling |
| Primary completion | 2025-09-30 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-09-30 | actual | The whole study's end, after follow-up |
| First posted | 2019-03-14 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-04-24 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Haemophilia B
Intervention
- Drug: Refixia®
Primary outcome
what the primary-completion date above is the date OFNumber of Adverse Reactions (ARs)
measured From baseline (week 0) to end of study (up to 6 years and 10 months)
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