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Taking people in GermanyPhase 3

Tests elecoglipron against placebo in adults with type 2 diabetes using insulin

Tests elecoglipron, compared with a placebo, in adults with type 2 diabetes on insulin.

Plain-language title generated from the registry record
Registry title: 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

Key facts

Where
Amberg, Bad Oeynhausen, Berlin, Duisburg, Eisenach, Elsterwerda, Falkensee, Frankfurt am Main, Gladbeck, Hamburg, Magdeburg, Mannheim, Münster, Nittendorf, Obertshausen, Oldenburg in Holstein, and Pirna, GermanySee the 17 sites
Phase
Phase 3

Where in Germany

  • Versdias GmbHAmberg, GermanyTaking people
  • Herz Und Diabeteszentrum NRW Bad Oeynhausen Universitaetsklinik Der Ruhr-Universitaet BochumBad Oeynhausen, GermanyTaking people
  • Medizinisches Versorgungszentrum Am Bahnhof Spandau GbRBerlin, GermanyTaking people
  • Diabetes Zentrum Duisburg MitteDuisburg, GermanyTaking people
  • Praxis für Diabetologie EisenachEisenach, GermanyTaking people
  • Zentrum fuer klinische Studien Suedbrandenburg GmbHElsterwerda, GermanyTaking people
  • Diabetes FalkenseeFalkensee, GermanyTaking people
  • IKF Pneumologie GmbH & Co. KGFrankfurt am Main, GermanyTaking people
  • Hausarztzentrum ButendorfGladbeck, GermanyTaking people
  • Diabeteszentrum Hamburg West (DZHW)Hamburg, GermanyTaking people
  • SMO.MD GmbHMagdeburg, GermanyTaking people
  • CRS Clinical Research Services Mannheim GmbHMannheim, GermanyTaking people
  • Schwerpunktpraxis Dr. KeuthageMünster, GermanyTaking people
  • Gemeinschaftspraxis NittendorfNittendorf, GermanyTaking people
  • Rahman & Detho Studien GmbHObertshausen, GermanyTaking people
  • R.E.D. Institut fuer medizinische Studien und Fortbildung GmbHOldenburg in Holstein, GermanyTaking people
  • Hausärztlich-diabetologische Praxis PirnaPirna, GermanyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
AstraZeneca
Trial code
NCT07664553EU 2025-523935-20-00
Record updated
4 August 2026
Original description
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)Read full original descriptionShow less

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)

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)

Inclusion: 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: 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; T1DM, secondary forms of diabetes (including congenital forms), or history of ketoacidosis or hyperosmolar coma; 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.

ClinicalTrials.gov NCT07664553 · EU CTIS 2025-523935-20-00