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Completed Phase 2 Interventional Results available

A Study of the Efficacy and Safety of PXL770 Versus Placebo After 12 Weeks of Treatment in Patients With NAFLD

ClinicalTrials.gov ID: NCT03763877

Public ClinicalTrials.gov record NCT03763877. 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 Nov 8, 2026, 4:31 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled, Parallel Group Trial to Assess the Efficacy and Safety of PXL770 Versus Placebo After 12 Weeks of Treatment in Patients With NAFLD

Brief summary

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

This study will assess the efficacy and safety of 3 doses of PXL770 versus placebo after 12 weeks of treatment.

Study identification

NCT ID
NCT03763877
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Poxel SA
Industry
Enrollment
121 participants

Conditions and interventions

Interventions

Drug

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
Mar 29, 2019 (Actual)
Primary completion
Aug 3, 2020 (Actual)
Completion
Aug 10, 2020 (Actual)
Last update posted
Oct 28, 2021

2019 – 2020

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Study Site 02 Los Angeles California 90057 —
Study Site 01 Gainesville Florida 32610 —
Study Site 11 Ocoee Florida 34761 —
Study Site 15 Orlando Florida 32804 —
Study Site 10 Athens Georgia 30607 —
Study Site 03 Indianapolis Indiana 46260 —
Study Site 07 Marrero Louisiana 70072 —
Study Site 05 West Monroe Louisiana 71291 —
Study Site 08 Berlin New Jersey 08009 —
Study Site 09 Durham North Carolina 27710 —
Study Site 13 Rapid City South Dakota 57701 —
Study Site 06 Arlington Texas 76012 —
Study Site 04 San Antonio Texas 78207 —
Study Site 12 San Antonio Texas 78215 —
Study Site 14 Richmond Virginia 23294 —

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 NCT03763877, 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 Oct 28, 2021 · Synced Nov 8, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03763877 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →