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Study on GS300 on NAFLD — REVERT  

Weight Loss Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Assessing the Effect of GS300 on Nonalcoholic Fatty Liver Disease

Clinical Trial Summary

To determine the efficacy of GS300 when administered for 24 weeks in patients with Nonalcoholic Fatty Liver Disease (NAFLD).

Clinical Trial Description

This is a multicenter, randomized, placebo-controlled, double-blinded, parallel-group study. Patients will be randomized 1:1 to receive either GS300 or placebo. The study includes an up to 6 weeks screening period, a 24-week treatment period, and a 1-week follow-up period. Approximately 250 patients (125 patients per arm) will be enrolled (at least 40% from each gender and at least 40% from US and 40% from Europe). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04887766
Study type Interventional
Source Gelesis, Inc.
Contact Valerie Colletta
Phone 1-857-201-5330
Email vcolletta@gelesis.com
Status Not yet recruiting
Phase N/A
Start date July 1, 2022
Completion date December 31, 2023
View Details
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