Adverse Event Data Collection From the EUHASS Registry on Turoctocog Alfa Pegol
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Phase
—
Status
Enrolling by invitation
Study type
Observational
Enrollment
50estimated
Sites
1
Country
Denmark
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 | 2020-12-09 | actual | When the study began enrolling |
| Primary completion | 2026-02-01 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2026-02-01 | estimated | The whole study's end, after follow-up |
| First posted | 2020-12-23 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-09-25 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Haemophilia A
Intervention
- Drug: Turoctocog alfa pegol
Primary outcome
what the primary-completion date above is the date OFAdverse events (AEs) reported to the registry with suspected relation to turoctocog alfa pegol, Adverse Drug Reactions (ADRs), in patients with haemophilia A for renal, hepatic and neurological events.
measured From start to end of data collection (December 2019 to January 2025)
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