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A 48-Month Study to Evaluate Long-Term Effectiveness of Elocta on Joint Health

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NCT04293523

Sponsored by Swedish Orphan Biovitrum (industry) · SOBI.ST — their whole pipeline →.

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
427actual
Sites
53
Countries
Czechia, Estonia, Finland +11

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
DateFiledBasisWhat it is
Start2020-03-30actualWhen the study began enrolling
Primary completionJul 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJul 2026estimatedThe whole study's end, after follow-up
First posted2020-03-03actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-03-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Hemophilia A

Intervention

  • Drug: ELOCTA — also filed as ELOCTATE, efmoroctocog alfa, rFVIIIFc

Primary outcomes

what the primary-completion date above is the date OF
Joint health: Target joint development
measured 48 months
Joint health: Target joint resolution
measured 48 months
Joint health: Target joint recurrence
measured 48 months
Joint health: Annualised joint bleeding rate (AJBR) for treated bleeds
measured 48 months

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