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Completed Phase 2 Interventional Results available

Safety, Tolerability, Pharmacokinetics and Efficacy of EYP001a in Patients With Nonalcoholic Steatohepatitis (NASH)

ClinicalTrials.gov ID: NCT03812029

Public ClinicalTrials.gov record NCT03812029. 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 Jul 23, 2026, 2:12 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 2a, Randomized, Double-Blind, Multicenter, Placebo-Controlled Study to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of EYP001a in Patients With Nonalcoholic Steatohepatitis

Study identification

NCT ID
NCT03812029
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Enyo Pharma
Industry
Enrollment
120 participants

Conditions and interventions

Interventions

  • Vonafexor Drug
  • Placebo Other

Drug · Other

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
Jan 29, 2019
Primary completion
Jun 15, 2021
Completion
Jul 5, 2021
Last update posted
May 5, 2023

2019 – 2021

United States locations

U.S. sites
24
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
ENYO PHARMA Investigative site 0424 North Little Rock Arkansas 72117
ENYO PHARMA Investigative site 0418 Lakewood Rch Florida 34211
ENYO PHARMA Investigative site 0402 Ocoee Florida 34761
ENYO PHARMA Investigative site 0420 Orlando Florida 32806
ENYO PHARMA Investigative site 0419 Port Orange Florida 32127
ENYO PHARMA Investigative site 0403 Athens Georgia 30607
ENYO PHARMA Investigative site 0423 Savannah Georgia 31406
ENYO PHARMA Investigative site 0407 Snellville Georgia 30078
ENYO PHARMA Investigative site 0409 Indianapolis Indiana 46260
ENYO PHARMA Investigative site 0413 Baton Rouge Louisiana 70809
ENYO PHARMA Investigative site 0404 Marrero Louisiana 70072
ENYO PHARMA Investigative site 0422 Baltimore Maryland 21202
ENYO PHARMA Investigative site 0412 Jackson Mississippi 39216
ENYO PHARMA Investigative site 0414 Kansas City Missouri 64131
ENYO PHARMA Investigative site 0406 Durham North Carolina 27710
ENYO PHARMA Investigative site 0411 Columbus Ohio 43213
ENYO PHARMA Investigative site 0401 Charleston South Carolina 29401
ENYO PHARMA Investigative site 0408 Charleston South Carolina 29407
ENYO PHARMA Investigative site 0421 Rapid City South Dakota 57701
ENYO PHARMA Investigative site 0405 Arlington Texas 76012
ENYO PHARMA Investigative site 0416 Austin Texas 78746
ENYO PHARMA Investigative site 0417 Edinburg Texas 78539
ENYO PHARMA Investigative site 0410 San Antonio Texas 78215
ENYO PHARMA Investigative site 0415 San Antonio Texas 78229

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 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03812029, 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 May 5, 2023 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03812029 live on ClinicalTrials.gov.

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