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Completed Phase 2 Interventional Results available

Study of PXL065 in Patients With Nonalcoholic Steatohepatitis (NASH)

ClinicalTrials.gov ID: NCT04321343

Public ClinicalTrials.gov record NCT04321343. 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 26, 2026, 12:20 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 36-week, Randomized, Double-blind, Placebo-controlled, Parallel Group Trial to Assess the Efficacy and Safety of PXL065 Versus Placebo in Noncirrhotic Biopsy-proven NonAlcoholic SteatoHepatitis (NASH) Patients

Brief summary

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

This study will assess the effect of 3 doses of PXL065 versus placebo on liver fat content in NASH patients after 36 weeks of treatment

Study identification

NCT ID
NCT04321343
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Poxel SA
Industry
Enrollment
117 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 31, 2020
Primary completion
Jun 7, 2022
Completion
Jun 19, 2022
Last update posted
Aug 28, 2023

2020 – 2022

United States locations

U.S. sites
29
U.S. states
11
U.S. cities
27
Facility City State ZIP Site status
Study site 11 Chandler Arizona 85224 —
Study site 12 Glendale Arizona 85306 —
Study site 13 Tucson Arizona 85712 —
Study site 21 Tucson Arizona 85712 —
Study site 17 Chula Vista California 91910 —
Study site 16 Fresno California 93720 —
Study site 04 Huntington Park California 90255 —
Study site 05 Los Angeles California 90057 —
Study site 22 Orange California 92866 —
Study site 06 Panorama City California 90402 —
Study site 07 Santa Ana California 92704 —
Study site 15 Boca Raton Florida 33434 —
Study site 31 Fort Myers Florida 33912 —
Study site 08 Port Orange Florida 32127 —
Study site 01 Sarasota Florida 34240 —
Study site 28 West Des Moines Iowa 50265 —
Study site 18 Kansas City Kansas 61431 —
Study site 24 Flowood Mississippi 39232 —
Study site 10 Jackson Mississippi 39216 —
Study site 27 East Syracuse New York 13057 —
Study site 14 Fayetteville North Carolina 28304 —
Study site 29 Summerville South Carolina 29485 —
Study site 25 Chattanooga Tennessee 37411 —
Study site 30 Clarksville Tennessee 37040 —
Study Site 02 Germantown Tennessee 38138 —
Study site 19 Austin Texas 78746 —
Study site 09 Edinburg Texas 78539 —
Study site 23 Edinburg Texas 78539 —
Pinnacle Clinical Research (Study site 20) 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04321343, 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 Aug 28, 2023 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04321343 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →