A Study to Assess How Well and Safely Elafibranor Works in Adult Participants With Primary Sclerosing Cholangitis
← catalyst calendarNCT07387549 · readout in 1,715 d
Sponsored by Ipsen (industry) · IPN.PA — their whole pipeline →.
Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
350estimated
Sites
6
Country
United States
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 | 2026-05-14 | actual | When the study began enrolling |
| Primary completion | 2031-04-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2031-05-31 | estimated | The whole study's end, after follow-up |
| First posted | 2026-02-04 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-03 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Primary Sclerosing Cholangitis
Interventions
- Drug: Elafibranor — also filed as IPN60190
- Other: Placebo
Primary outcome
what the primary-completion date above is the date OFEvent-Free Survival
measured From baseline until the end of treatment (estimated up to 5 years)
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