Trial intelligence / Profile preview

DA-302168S in Overweight/Obese Subjects

NCT06541730Phase 1Completed

Sponsor
Chengdu Diao Pharmaceutical Group
Start
Aug 2024
Primary completion
Jan 2025
Modality
Small Molecules
Countries
1
01

Overview

Phase 1, randomised, double-blind trial in obesity and Overweight comparing DA-302168S with Placebo (2 arms). Primary endpoint: Incidence of Treatment-Emergent Adverse Events at 49 days. Started Aug 2024; status: completed.

02

Drugs

DA-302168S
03

Conditions

obesityOverweight

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