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Completed Phase 2 Interventional Results available

Emricasan, an Oral Caspase Inhibitor, in Subjects With NASH Cirrhosis and Severe Portal Hypertension

ClinicalTrials.gov ID: NCT02960204

Public ClinicalTrials.gov record NCT02960204. 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 Oct 26, 2026, 2:49 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial of Emricasan, an Oral Caspase Inhibitor, in Subjects With Non-Alcoholic Steatohepatitis (NASH) Cirrhosis and Severe Portal Hypertension

Brief summary

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

This is a multicenter, randomized, double-blind, placebo-controlled trial involving subjects with NASH cirrhosis and severe portal hypertension (defined as HVPG ≥12 mmHg as determined by the central reader assigned to this study). Upon successful screening, subjects will be randomized to receive either emricasan 50 mg BID, 25 mg BID, or 5 mg BID or matching placebo BID.

Study identification

NCT ID
NCT02960204
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Histogen
Industry
Enrollment
263 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Oct 17, 2016 (Actual)
Primary completion
Oct 2, 2018 (Actual)
Completion
Apr 8, 2019 (Actual)
Last update posted
Feb 11, 2022

2016 – 2019

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Pasadena Pasadena California 91105 —
Rialto Rialto California 92377 —
Palmetto Bay Palmetto Bay Florida 33157 —
Atlanta Atlanta Georgia 30309 —
Clive Clive Iowa 50325 —
Baltimore Baltimore Maryland 21202 —
Detroit Detroit Michigan 48202 —
Rochester Rochester Minnesota 55905 —
Saint Paul Saint Paul Minnesota 55114 —
Kansas City Kansas City Missouri 64131 —
Durham Durham North Carolina 27710 —
Philadelphia Philadelphia Pennsylvania 19104 —
Philadelphia Philadelphia Pennsylvania 19141 —
Germantown Germantown Tennessee 38138 —
Arlington Arlington Texas 76012 —
Houston Houston Texas 77030 —
San Antonio San Antonio Texas 78215 —
San Antonio San Antonio Texas 78233 —
Norfolk Norfolk Virginia 23502 —
Richmond Richmond Virginia 23226 —
Richmond Richmond Virginia 23249 —
Seattle, Washington 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02960204, 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 Feb 11, 2022 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02960204 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →