Drugs / EDP-297
last change Nov 2022 re-read 3 minutes ago

EDP-297

Investigated by
Enanta Pharmaceuticals, Inc · PRA Health Sciences

Trials 1

202120222023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT04559126 Sep 2020 → Jun 2021 metabolic dysfunction-associated steatohepatitis Enanta Pharmaceuticals, Inc Completed No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2021-10-04 Enanta Pharmaceuticals, Inc Results Enanta Pharmaceuticals Provides Update on NASH FXR Agonist Programs enanta.com ↗
A pre-planned interim analysis of a subset of patients through week 12 in the Phase 2b ARGON-2 study of EDP-305 as a monotherapy and data from its Phase 1 clinical study of EDP-297 provided meaningful information on dose selection and characterization for these compounds.
2020-08-28 Enanta Pharmaceuticals, Inc Results Enanta Pharmaceuticals Presents New Data from its Hepatitis B and Non-Alcoholic Steatohepatitis Programs at the Digital International Liver Congress™ 2020 enanta.com ↗
Preclinical Findings for Follow-on FXR Agonist EDP-297 Targeting NASH, Demonstrating Potent Anti-Fibrotic, Anti-Inflammatory and Hepatoprotective Effects

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 2 sources stand behind the page.

FieldValueCited text
Known as EDP-297 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04559126 ↗
Action Activate “EDP-297 is a farnesoid X receptor agonist” PMID 36369848 ↗ Nov 2022
Route Oral “orally administered single and multiple doses of EDP-297” NCT04559126 ↗