Purpose

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).

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Legal age of consent and at least 18 years old - Study 1 - - BMI ≥ 30 kg/m2 or - 25 kg/m2 ≤ BMI < 30 kg/m2 with at least one of the following weight-related comorbidities: - Hypertension - Prediabetes - Dyslipidemia - Cardiovascular disease - Obstructive sleep apnea. - Study 2 - BMI ≥ 25 kg/m2 and T2DM defined as below: - Established diagnosis of T2DM - Without established diagnosis of T2DM and HbA1c ≥ 6.5% (48 mmol/mol) at the screening visit - Stable body weight (self-reported or documented) for 90 days prior to the screening visit (± 5% body weight change) - History of at least one self-reported unsuccessful dietary effort to lose body weight.

Exclusion Criteria

  • Study 1 - Established diagnosis of T1DM or T2DM. - Study 2 - Any of the following medical history, laboratory values, or complications related to diabetes: - 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. - Have had more than one episode of severe hypoglycemia within 180 days prior to the screening visit, or has a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms - History of acute (unless due to previously resolved gallstone pancreatitis and post-cholecystectomy) or chronic pancreatitis - History/family history (first degree biologic relatives) of medullary thyroid cancer or multiple endocrine neoplasia type 2

Study Design

Phase
Phase 3
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Arm 1 - Dose 1
Active IMP
  • Drug: Elecoglipron
    Elecoglipron film-coated tablet once daily
    Other names:
    • Active IMP
Experimental
Arm 2 - Dose 2
Active IMP
  • Drug: Elecoglipron
    Elecoglipron film-coated tablet once daily
    Other names:
    • Active IMP
Placebo Comparator
Arm 3 - Placebo
Placebo matching elecoglipron
  • Drug: Placebo
    Placebo matching elecoglipron film-coated tablet once daily

More Details

Status
Recruiting
Sponsor
AstraZeneca

Study Contact

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

Detailed Description

This is a Phase III, global, randomized, parallel-group, double-blind, placebo-controlled, multicenter study to assess the efficacy and safety of 2 doses of elecoglipron compared with placebo, given once daily as oral tablets. This protocol covers two independent pivotal studies in adults aged 18 years and above, who are living with obesity (BMI ≥ 30 kg/m2), or overweight (BMI ≥ 25 kg/m2) and have at least 1 weight-related comorbidity (Hypertension, Prediabetes, Dyslipidemia, CV disease and/or Obstructive sleep apnea) without T2DM (Study 1) and as well as those who are living with obesity or overweight with T2DM (Study 2). Approximately 3000 participants will be randomized in the study 1 and 1500 participants in the study 2. The primary endpoint is percent change in body weight from baseline at 72 weeks.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.