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Completed Phase 2 Interventional Results available

Study of Safety, Tolerability, and Efficacy of a Combination Treatment of LJN452 and CVC in Adult Patients With NASH and Liver Fibrosis

ClinicalTrials.gov ID: NCT03517540

Public ClinicalTrials.gov record NCT03517540. 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 2, 2026, 3:26 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 Randomized, Double-blind, Multicenter Study to Assess the Safety, Tolerability, and Efficacy of a Combination Treatment of Tropifexor (LJN452) and Cenicriviroc (CVC) in Adult Patients With Nonalcoholic Steatohepatitis (NASH) and Liver Fibrosis

Brief summary

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

The purpose of this study was to assess the safety, tolerability, and efficacy of a combination treatment of tropifexor (LJN452) and cenicriviroc (CVC) in adult patients with nonalcoholic steatohepatitis (NASH) and liver fibrosis.

Study identification

NCT ID
NCT03517540
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
193 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
Sep 10, 2018
Primary completion
Sep 14, 2020
Completion
Oct 14, 2020
Last update posted
Apr 28, 2022

2018 – 2020

United States locations

U.S. sites
27
U.S. states
14
U.S. cities
24
Facility City State ZIP Site status
Novartis Investigative Site Chandler Arizona 85224
Novartis Investigative Site North Little Rock Arkansas 72117
Novartis Investigative Site Coronado California 92118
Novartis Investigative Site Los Angeles California 90048
Novartis Investigative Site Los Angeles California 90057
Novartis Investigative Site Pasadena California 91105
Novartis Investigative Site Rialto California 92377
Novartis Investigative Site Atlanta Georgia 30309
Novartis Investigative Site Atlanta Georgia 30312
Novartis Investigative Site Marietta Georgia 30060
Novartis Investigative Site Chicago Illinois 60637-1470
Novartis Investigative Site Indianapolis Indiana 46237
Novartis Investigative Site Metairie Louisiana 70006
Novartis Investigative Site Shreveport Louisiana 71103
Novartis Investigative Site Concord North Carolina 28027
Novartis Investigative Site Durham North Carolina 27710
Novartis Investigative Site Morehead City North Carolina 28557
Novartis Investigative Site Providence Rhode Island 02905
Novartis Investigative Site Chattanooga Tennessee 37404
Novartis Investigative Site Germantown Tennessee 38138
Novartis Investigative Site Hermitage Tennessee 37076
Novartis Investigative Site Dallas Texas 75208-2312
Novartis Investigative Site San Antonio Texas 78215
Novartis Investigative Site Murray Utah 84107
Novartis Investigative Site Richmond Virginia 23249
Novartis Investigative Site Richmond Virginia 23298
Novartis Investigative Site 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 38 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03517540, 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 Apr 28, 2022 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03517540 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →