A Study of RGT001-075 in Participants With Obesity or Overweight With Weight-Related Comorbidities
Completed · Phase 2 · Has a placebo group
Conditions studied: Obesity
In brief
The main purpose of this study was to evaluate the safety and tolerability of RGT001-075 in healthy participants with obesity
Key facts
- Study ID
- NCT06277934
- Run by
- Regor Pharmaceuticals Inc.
- People needed
- 73
- Starts
- 2024-03-08
- Expected to finish
- 2024-08-13
- Last updated by the study team
- 2025-08-07
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 and ≤ 75 years
- Have a BMI ≥27 kg/m² and ≤ 45 kg/m²
- Have had a stable body weight for the 3 months prior to randomization
You may not qualify if…
- Have obesity induced by other endocrinologic disorders or diagnosed monogenetic or syndromic forms of obesity
- Have a prior or planned surgical treatment for obesity
- Have or plan to have endoscopic and/or device-based therapy for obesity
- Have any prior diagnosis of diabetes
- Have an electrocardiogram (ECG) with abnormalities
- Have a history of Major Depressive Disorder (MDD) or other severe psychiatric disorders within the last 2 years
- Have a history of suicide attempt.
Where it is running
- Velocity Clinical Research — Los Angeles, California, United States
- Velocity Clinical Research — Valparaiso, Indiana, United States
- Velocity Clinical Research — Omaha, Nebraska, United States
- Velocity Clinical Research — Vestal, New York, United States
- Velocity Clinical Research — Durham, North Carolina, United States
- Velocity Clinical Research — Cleveland, Ohio, United States
- Velocity Clinical Research — Medford, Oregon, United States
- Velocity Clinical Research — East Greenwich, Rhode Island, United States
- Velocity Clinical Research — Dallas, Texas, United States
- Velocity Clinical Research — West Jordan, Utah, United States
Full record on ClinicalTrials.gov
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