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

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorAstraZeneca

About this trial

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).

Eligibility criteria

Qualifiers

Legal age of consent and at least 18 years old

Study 1 -

BMI ≥ 30 kg/m2 or

Hypertension

Disqualifiers

Study 1 - Established diagnosis of T1DM or T2DM.

T1DM

HbA1c ≥ 10% (86 mmol/mol) at the screening visit

Currently receiving, or anticipated to receive, therapeutic intervention for diabetic retinopathy and/or macular edema.

Trial design

Treatments tested in this trial

  • Elecoglipron
  • Placebo

Treatment groups

4,500 Participants
are divided into 3 treatment groups

Sponsors and collaborators