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A 16-Week Study to Evaluate the Efficacy, Safety, and Tolerability of GLY-200 in Participants With Obesity

Obesity Clinical Trial

Official title:
A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of GLY-200 in Participants With Obesity

Clinical Trial Summary

This study will evaluate the efficacy, safety, and tolerability of GLY-200 in participants with obesity.

Clinical Trial Description

This study is a Phase 2, randomized, double-blind, placebo-controlled, multi-center study in adult participants with obesity. Approximately 70 participants will be randomized in a 1:1 ratio to GLY-200 (2.0 g, twice daily) or placebo (twice daily). There will be a ≤ 28-day screening period. Dosing will occur for 16 weeks. Clinic visits will occur at Screening, Week 0 (Day 1), and Weeks 1, 2, 4, 6, 8, 12, 16, and 17 [End of Study (EOS)] or Early Termination (ET). Phone visits will occur at Week 3, 10, and 14. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06259981
Study type Interventional
Source Glyscend, Inc.
Contact Rachael Farley
Phone 513-579-9911
Email R.farley@medpace.com
Status Recruiting
Phase Phase 2
Start date May 20, 2024
Completion date December 2024
View Details
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