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Not yet recruiting Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT07667803

Public ClinicalTrials.gov record NCT07667803. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 25, 2026, 8:08 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Randomized, Double-blind, Placebo-controlled Multicenter Master Protocol to Evaluate the Efficacy and Safety of Elecoglipron in Participants With Obesity or Overweight With or Without Type 2 Diabetes Mellitus (Embold)

Study identification

NCT ID
NCT07667803
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
4,500 participants

Conditions and interventions

Interventions

  • Elecoglipron Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 5, 2026
Primary completion
Jul 30, 2028
Completion
Jul 29, 2029
Last update posted
Jun 24, 2026

2026 – 2029

United States locations

U.S. sites
26
U.S. states
19
U.S. cities
26
Facility City State ZIP Site status
Research Site Birmingham Alabama 35205
Research Site Chandler Arizona 85225
Research Site Lincoln California 95648
Research Site Clearwater Florida 33765
Research Site Woodstock Georgia 30189
Research Site Indianapolis Indiana 46254
Research Site Louisville Kentucky 40213
Research Site Baltimore Maryland 21229
Research Site Potomac Maryland 20854
Research Site Ypsilanti Michigan 48197
Research Site Kansas City Missouri 64114
Research Site Albany New York 12205
Research Site Laurelton New York 11413
Research Site Greensboro North Carolina 27408
Research Site Raleigh North Carolina 27609
Research Site Rocky Mount North Carolina 27804
Research Site Statesville North Carolina 28625
Research Site Dayton Ohio 45424
Research Site Tulsa Oklahoma 74133
Research Site DuBois Pennsylvania 15801
Research Site Newport Pennsylvania 17074
Research Site Gaffney South Carolina 29340
Research Site Franklin Tennessee 37067
Research Site Knoxville Tennessee 37912
Research Site Dallas Texas 75254
Research Site Morgantown West Virginia 26501

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 106 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07667803, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 24, 2026 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07667803 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →