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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


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

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