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A Phase III Study to Investigate the Efficacy and Safety of Elecoglipron Compared With Placebo in Adults With Type 2 Diabetes Mellitus on Background Insulin
A Randomized, Double-blind, Parallel-group Phase III Study to Evaluate the Efficacy, Safety, and Tolerability of Elecoglipron Compared With Placebo in Adults With Type 2 Diabetes Mellitus on Background Insulin (Eluminate-3)
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Diagnosed with T2DM for at least 90 days prior to screening * Stable treatment with background insulin and other background glucose-lowering medication(s) * HbA1c value of ≥ 7% to ≤ 10.5% * Body mass index (BMI) of ≥ 23 kg/m2 at screening * Stable body weight (self-reported or documented) for 90 days prior to screening Exclusion Criteria: * T1DM, secondary forms of diabetes (including congenital forms), or history of ketoacidosis or hyperosmolar coma * Currently receiving or anticipated to receive, therapeutic intervention for diabetic retinopathy and/or macular edema * Have had more than one episode of severe hypoglycemia within 180 days prior to screening or has a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms * Clinically significant condition affecting the upper GI tract or chronic use of any medication that affects gastric motility or gastric emptying * History of acute or chronic pancreatitis. * Severe congestive heart failure (NYHA IV) * History/family history of medullary thyroid cancer or multiple endocrine neoplasia type 2
About the study
The purpose of this study is to evaluate the efficacy, safety, and tolerability of elecoglipron compared with placebo in adults with Type 2 Diabetes Mellitus (T2DM), treated with a background insulin and other background glucose-lowering medication(s)
What is being tested
- Elecoglipron (drug)
- Placebo (drug)
Sponsor: AstraZeneca · Participants: 600 · Started: Jul 8, 2026
Contact the study team
- AstraZeneca Clinical Study Information Center · Phone: 1-877-240-9479
Official record on ClinicalTrials.gov — NCT07664553
Locations in the U.S.
| Arkansas | Research Site, Little Rock (Not yet recruiting) |
| California | Research Site, Sacramento (Not yet recruiting) |
| Colorado | Research Site, Aurora (Not yet recruiting) |
| Florida | Research Site, Doral (Not yet recruiting) Research Site, Ocoee |
| Georgia | Research Site, Decatur (Not yet recruiting) |
| Maryland | Research Site, Potomac (Not yet recruiting) |
| North Carolina | Research Site, Cary (Not yet recruiting) Research Site, Morehead City (Not yet recruiting) |
| South Carolina | Research Site, Myrtle Beach (Not yet recruiting) |
| Tennessee | Research Site, Memphis (Not yet recruiting) |
| Texas | Research Site, Houston (Not yet recruiting) Research Site, Round Rock (Not yet recruiting) Research Site, San Antonio (Not yet recruiting) |
| Washington | Research Site, Renton (Not yet recruiting) |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.