Drugs / Lanifibranor

Trials 5

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 12 trials
Phase 1 NCT06126562 Oct → Nov 2023 — Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Completed No outcome recorded
Phase 1 NCT03866369 Jan → Aug 2019 — Inventiva Pharma Completed No outcome recorded
Phase 22 trials · 1 met primary
Phase 2 NCT05232071 Jun 2022 → May 2024 metabolic dysfunction-associated steatohepatitis, type 2 diabetes mellitus Inventiva Pharma Completed No outcome recorded
Phase 2 NCT03008070 Feb 2017 → Feb 2020 metabolic dysfunction-associated steatohepatitis Inventiva Pharma Completed Met primary
Phase 31 trial
Phase 3 NCT04849728 Aug 2021 → Sep 2027 expected metabolic dysfunction-associated steatohepatitis Inventiva Pharma Active not recruiting No outcome recorded
Comparator or background therapy2 trials
Phase 2 NCT03459079 Comparator Aug 2018 → Apr 2023 NAFLD1, type 2 diabetes mellitus University of Florida Completed No outcome recorded
Phase 2 NCT02503644 Comparator Oct 2015 → Oct 2018 diffuse cutaneous systemic sclerosis, diffuse scleroderma Inventiva Pharma Completed No outcome recorded

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 9 sources stand behind the page.

FieldValueCited text
Known as lanifibranor “Lanifibranor (IVA337), a panPPAR agonist, by acting on these three different PPAR isotypes, combines pharmacological effects that could address the different components of the...” PMID 33038502 ↗ Oct 2020
4

NCT05232071 ↗

NCT03866369 ↗

NCT06126562 ↗

NCT03459079 ↗

Known as IVA337 “Multiple Ascending Dose Phase I Study in Order to Define Lanifibranor (IVA337) Supra-thjerapeutic Dose” NCT03866369 ↗
3

“Drug: IVA337” NCT04849728 ↗

NCT02503644 ↗

NCT03008070 ↗

Action Activate “IVA337 (lanifibranor) is a next generation pan-PPAR (peroxisome proliferator-activated receptors) agonist addressing the pathophysiology of NASH : metabolic, inflammatory and fibrotic.” NCT03008070 ↗
Modality Small molecule — CHEMBL4091374 ↗
Route Oral “Single daily oral dose during 14 days” NCT03866369 ↗