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A Phase III Study to Investigate the Efficacy and Safety of the Combination of Elecoglipron and Dapagliflozin in Adults With Type 2 Diabetes Mellitus

NCT07662109

This study is recruiting at 17 US sites in 14 states, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of this study is to evaluate the efficacy, safety, and tolerability of elecoglipron and dapagliflozin in combination, compared with elecoglipron alone and dapagliflozin alone, in adults with type 2 diabetes mellitus (T2DM) inadequately managed with lifestyle management alone or treated with other background glucose-lowering medication.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Type 2 Diabetes Mellitus

Eligibility basics and study details

Study type
Interventional
Phase
Phase 3
Ages
18 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
AstraZeneca
Last updated on ClinicalTrials.gov
October 30, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Arkansas · 1

  • Research Site · Little Rock, AR

California · 1

  • Research Site · Los Angeles, CA

Florida · 2

  • Research Site · Lake City, FL
  • Research Site · Lakeland, FL

Illinois · 1

  • Research Site · Chicago, IL

Maryland · 1

  • Research Site · Oxon Hill, MD

Michigan · 1

  • Research Site · Troy, MI

Mississippi · 1

  • Research Site · Ridgeland, MS

New Mexico · 1

  • Research Site · Albuquerque, NM

New York · 1

  • Research Site · Brooklyn, NY

Ohio · 1

  • Research Site · Maumee, OH

Tennessee · 2

  • Research Site · Kingsport, TN
  • Research Site · Nashville, TN

Texas · 2

  • Research Site · Dallas, TX
  • Research Site · Paris, TX

Virginia · 1

  • Research Site · Newport News, VA

West Virginia · 1

  • Research Site · Kingwood, WV

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.