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Study identifier: NCT07667803 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Master Protocol to Investigate Efficacy and Safety of Elecoglipron in Participants With Obesity or Overweight With or Without T2DM

Condition: Weight Management  ·  Sponsor: AstraZeneca

PhasePhase 3
Planned participants4500
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This master study protocol, Study D7260C00015, covers 2 independent, pivotal studies, Study 1 and Study 2. Each study is a global, randomized, double-blind, parallel-group, multicenter, Phase III study to assess the efficacy and safety of elecoglipron compared with placebo adjunct to diet and exercise for weight management, in adults living with obesity or overweight with at least one weight-related comorbidity, and without T2DM (Study 1) or with T2DM (Study 2).

This description comes directly from the study's public registry record.

Talk to the study team

AstraZeneca Clinical Study Information Center  ·  1-877-240-9479  ·  information.center@astrazeneca.com

Always discuss trial participation with your own doctor first.

Locations (321)

Research SiteBirmingham, Alabama, United StatesNot Yet Recruiting
Research SiteDothan, Alabama, United StatesNot Yet Recruiting
Research SiteChandler, Arizona, United StatesNot Yet Recruiting
Research SitePeoria, Arizona, United StatesNot Yet Recruiting
Research SiteLittle Rock, Arkansas, United StatesNot Yet Recruiting
Research SiteLynwood, California, United StatesNot Yet Recruiting
Research SiteRolling Hills Estates, California, United StatesNot Yet Recruiting
Research SiteSacramento, California, United StatesNot Yet Recruiting
Research SiteArvada, Colorado, United StatesNot Yet Recruiting
Research SiteNew Haven, Connecticut, United StatesNot Yet Recruiting
Research SiteClearwater, Florida, United StatesNot Yet Recruiting
Research SitePlantation, Florida, United StatesNot Yet Recruiting

+ 309 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07667803