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Completed Phase 2 Interventional Results available

Study to Evaluate Safety, Tolerability, and Efficacy of GS-0976 in Adults With Nonalcoholic Steatohepatitis

ClinicalTrials.gov ID: NCT02856555

Public ClinicalTrials.gov record NCT02856555. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 12:53 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Safety, Tolerability, and Efficacy of GS-0976 in Subjects With Nonalcoholic Steatohepatitis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to evaluate the safety and tolerability of firsocostat in adults with nonalcoholic steatohepatitis (NASH).

Study identification

NCT ID
NCT02856555
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gilead Sciences
Industry
Enrollment
127 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 7, 2016
Primary completion
Jul 17, 2017
Completion
Jul 17, 2017
Last update posted
Jul 23, 2020

2016 – 2017

United States locations

U.S. sites
36
U.S. states
17
U.S. cities
30
Facility City State ZIP Site status
Not listed Coronado California 92118
Not listed Foster City California 94404
Not listed Los Angeles California 90036
Not listed Los Angeles California 90048
Not listed Rialto California 92377
Not listed San Diego California 92103
Not listed San Diego California 92123
Not listed San Francisco California 94115
Not listed San Francisco California 94143
Not listed Miami Florida 33136
Not listed Miami Florida 33165
Not listed Atlanta Georgia 30308
Not listed Chicago Illinois 60611
Not listed Indianapolis Indiana 46202
Not listed New Orleans Louisiana 70112
Not listed Boston Massachusetts 02115
Not listed Rochester Minnesota 55905
Not listed Kansas City Missouri 64131
Not listed New York New York 10016
Not listed Durham North Carolina 27710
Not listed Statesville North Carolina 28677
Not listed Philadelphia Pennsylvania 19707
Not listed Pittsburgh Pennsylvania 15213
Not listed Germantown Tennessee 38138
Not listed Memphis Tennessee 38104
Not listed Nashville Tennessee 37211
Not listed Arlington Texas 76012
Not listed Live Oak Texas 78233
Not listed San Antonio Texas 78215
Not listed Murray Utah 84107
Not listed Falls Church Virginia 22042
Not listed Richmond Virginia 23226
Not listed Richmond Virginia 23249
Not listed Richmond Virginia 23298
Not listed Richland Washington 99352
Not listed Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02856555, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 23, 2020 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02856555 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →