Condition: Obesity · Overweight · Type 2 Diabetes · Sponsor: Eli Lilly and Company
The purpose of this Master Protocol is to support two studies to see how well and how safely orforglipron works compared to placebo in participants who have obesity or overweight with or without type 2 diabetes. Participants will be screened for about 4 weeks, after which they will enroll into either J2A-MC-GZP1, NCT06972459 (do not have type 2 diabetes) or J2A-MC-GZP2, NCT06972472 (have type 2 diabetes).
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Clinical Research Institute of Arizona (CRI) - Sun City West | Sun City West, Arizona, United States | — |
| Novak Clinical Research - Tucson - North La Cholla Boulevard | Tucson, Arizona, United States | — |
| Norcal Endocrinology & Internal Medicine | San Ramon, California, United States | — |
| Southern California Clinical Research | Santa Ana, California, United States | — |
| Care Access - Thousand Oaks | Thousand Oaks, California, United States | — |
| Accel Research Sites - DeLand Clinical Research Unit | DeLand, Florida, United States | — |
| Innovation Medical Research Center - Fort Lauderdale | Fort Lauderdale, Florida, United States | — |
| Indago Research & Health Center, Inc | Hialeah, Florida, United States | — |
| Encore Medical Research | Hollywood, Florida, United States | — |
| West Orange Endocrinology P.A. | Ocoee, Florida, United States | — |
| Care Access - Tampa | Tampa, Florida, United States | — |
| Conquest Research | Winter Park, Florida, United States | — |
+ 68 more locations — full list on the registry record.
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