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Active Not RecruitingNCT06066528

A Study to Test Whether Survodutide (BI 456906) Helps People Living With Overweight or Obesity Who Also Have Diabetes to Lose Weight

A Phase 3, Randomised, Double-blind, Parallel-group, 76-week, Efficacy and Safety Study of BI 456906 Administered Subcutaneously Compared With Placebo in Participants With Overweight or Obesity and Type 2 Diabetes Mellitus

Status
Active Not Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
755 (actual)
Sponsor
Boehringer Ingelheim · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is open to adults who are at least 18 years old and have a body mass index of 27 kg/m² or more. People can take part if they have type 2 diabetes and if they are currently being treated only with diet and exercise or with specific diabetes medications. Only people who have previously not managed to lose weight by changing their diet can participate. The purpose of this study is to find out whether a medicine called survodutide (BI 456906) helps people living with overweight or obesity who also have diabetes to lose weight. Participants are divided into 3 groups by chance, like drawing names from a hat. 2 groups get different doses of survodutide and 1 group gets placebo. Placebo looks like survodutide but does not contain any medicine. Every participant has a 2 in 3 chance of getting survodutide. Participants inject survodutide or placebo under their skin once a week for about one and a half years. In addition to the study medicine, all participants receive counselling to make changes to their diet and to exercise regularly. Participants are in the study for about 1 year and 7 months. During this time, it is planned that participants visit the study site up to 14 times and receive 6 phone calls by the site staff. The doctors check participants' health and take note of any unwanted effects. The study staff also regularly measure participants' body weight. The results are compared between the groups to see whether the treatment works.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTSurvodutideonce weekly subcutaneous injection, pre-filled syringe
COMBINATION_PRODUCTPlaceboonce weekly subcutaneous injection, pre-filled syringe

Timeline

Start date
2023-11-27
Primary completion
2025-12-12
Completion
2026-04-03
First posted
2023-10-04
Last updated
2026-04-02

Locations

143 sites across 19 countries: United States, Australia, Belgium, Canada, China, Czechia, Denmark, Finland, Germany, Greece, Hungary, Japan, Netherlands, New Zealand, Poland, South Korea, Spain, Sweden, United Kingdom

Regulatory

Source: ClinicalTrials.gov record NCT06066528. Inclusion in this directory is not an endorsement.