CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 726 enrolled
Drug / intervention
survodutide +1 morecombination
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06066515
NCT06066515Phase 3Completed

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 Without Type 2 Diabetes

Boehringer Ingelheim·interventional·Posted Oct 4, 2023·Updated Mar 12, 2026

In Brief

A Phase 3 clinical trial evaluating survodutide and Placebo for Obesity. Completed, enrolled 726 participants across 118 sites in 14 countries.

Detailed Summary

This study is open to adults who are at least 18 years old and have * a body mass index (BMI) of 30 kg/m² or more, or * a BMI of 27 kg/m² or more and at least one health problem related to their weight. People with type 2 diabetes cannot take part in this study. 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 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 participants' body weight is regularly measured. The results are compared between the groups to see whether the treatment works.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsObesity
CountriesAustralia, Belgium, Canada, China, Finland, Germany, Japan, Netherlands, New Zealand, Poland, South Korea, Sweden, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
202420252026
First PostedOct 4, 2023
Enrollment StartNov 25, 2023
Primary CompletionDec 2, 2025
Study CompletionFeb 20, 2026
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 2.7 years ago

Interventions

survodutidecombination

once weekly subcutaneous injection

Placebocombination

once weekly subcutaneous injection