CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 171 enrolled
Drug / intervention
NGM282 +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03912532
NCT03912532Phase 2Completed

A Phase 2b, Randomized, Double-blind, Placebo-controlled, Multi-center Study to Evaluate the Efficacy, Safety, and Tolerability of Three Doses of NGM282 Administered for 24 Weeks for the Treatment of Histologically Confirmed Nonalcoholic Steatohepatitis (NASH)

NGM Biopharmaceuticals, Inc·interventional·Posted Apr 11, 2019·Updated Jul 3, 2025

In Brief

A Phase 2 clinical trial evaluating NGM282 and Placebo for NASH - Nonalcoholic Steatohepatitis. Completed, enrolled 171 participants across 37 sites in 2 countries.

Detailed Summary

This is a multi-center evaluation of NGM282 in a randomized, double-blind, placebo-controlled study administered for 24 weeks in participants with histologically confirmed NASH and F2/F3 Fibrosis.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesPuerto Rico, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2020202120222023202420252026
First PostedApr 11, 2019
Enrollment StartMay 16, 2019
Primary CompletionMar 4, 2021
Study CompletionMar 29, 2021
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 7.2 years ago

Interventions

NGM282biological

NGM282

Placeboother

Placebo for NGM282