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2025-524385-18-00CompletedPhase 1

A Randomised, Open-Label, Single-Centre, Study to Evaluate the Bioequivalence of Lanifibranor

Source: EU CTIS (euclinicaltrials.eu) · Last updated 4 Feb 2026

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
30 (actual)
First submitted
21 Nov 2025
Start date
Feb 2026
Lead sponsor
Inventiva
EU CT number
2025-524385-18-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 30
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
BiotrialRennesFranceCompleted

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.