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A Study to Evaluate the Effects of Enicepatide in Participants With Obesity or Overweight, With or Without Type 2 Diabetes
A Study to Evaluate the Effects of Enicepatide in Participants With Obesity or Overweight, With or Without Type 2 Diabetes

NCT07670416

RecruitingPhase 3

Sponsor: Hoffmann-La Roche

Conditions: Obesity, Overweight, Type 2 Diabetes Mellitus (T2DM)

Interventions: Enicepatide, Placebo

Countries: China

The purpose of this study is to assess the efficacy and safety of enicepatide, a dual glucagon-like peptide-1 (GLP-1)/glucose-dependent insulinotropic polypeptide (GIP) receptor agonist (RA) being developed for chronic weight management, as an adjunct to a reduced-calorie diet and increased physical activity in participants without Type 2 diabetes mellitus (T2DM) who have obesity or overweight with at least one weight-related comorbidity, and in participants with T2DM who have obesity or overweight.

Eligibility overview

Sex: ALL

Age: 18 Years to

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Body mass index (BMI) ≥24.0 kilograms per meter squared (kg/m\^2) for participants with type 2 diabetes mellitus (T2DM)
* BMI ≥28.0 kg/m\^2 or BMI ≥24.0 and \<28.0 kg/m\^2 and diagnosed with at least one weight-related comorbidity (prediabetes, hypertension, dyslipidemia, fatty liver, obstructive sleep apnea, or weight-related cardiovascular disease) for participants without T2DM
* Agreement to adhere to the contraception requirements

Exclusion Criteria:

* History of Type 1 diabetes mellitus (T1DM)
* Obesity induced by other endocrinologic disorders
* Any planned major medical procedure or surgery during the study
* History of significant active or unstable major depressive disorder (MDD) or other severe psychiatric disorder
* Any lifetime history of suicide attempt
* History of any hematologic conditions that may interfere with HbA1c measurement
* History of acute or chronic pancreatitis or clinically significant gallbladder disease
* Treatment with any approved or investigational GLP-1-RA-based therapy within 6 months prior to randomization
* Treatment with other investigational therapy within 3 months prior to randomization or less than 5 elimination half-lives prior to randomization, whichever is longer
* Known allergy to any component of the study drug formulation or any other condition that is a contraindication to GLP-1 RAs or GLP-1/GIP RAs
Locations (12)
  • Xianyang, Shaanxi, China
  • Ningbo, Zhejiang, China
  • Beijing, China
  • Jinan, China
  • Langfang, China
  • Luoyang, China
  • Shanghai, China
  • Shanghai, China
  • Shanghai, China
  • Shanghai, China
  • Shijiazhuang, China
  • Zibo, China