GLPwatch

A Study to Test Whether BI 456906 (Survodutide) Influences the Amount of Bupropion, Caffeine and Midazolam in the Blood in People With Overweight or Obesity

NCT06564441 · Completed

Last updated 2026-05-28

This clinical trial is testing whether the drug BI 456906 (survodutide) affects the levels of bupropion, caffeine, and midazolam in the blood of adults who are overweight or have obesity.

Status Completed The study has finished.
Phase Phase 1 Checks safety and dosing in a small group.
Type Interventional (clinical trial)
Design open-label (no blinding) treatment study
Participants 34 people
Who can join Ages 18–60 · all sexes Healthy volunteers accepted.
Timeline Started 2024-10 · est. completion 2026-01
Where 1 site · Belgium

What this study is testing ClinicalTrials.gov NCT06564441 ↗

Description as written by the study sponsor.

This study is open to adults with overweight or obesity who are otherwise healthy. People can join the study if they have a body mass index of 27 to 39.9 kg/m2 and a body weight over 70 kg. The purpose of this study is to find out whether taking multiple doses of BI 456906 influences the amount of bupropion, caffeine, and midazolam in the blood. The study has 2 treatment periods. In Period 1, participants take 1 dose each of midazolam, caffeine, and bupropion as tablets or oral solution on separate days. In Period 2, participants get BI 456906 as an injection under the skin once a week. At 2 selected timepoints in Period 2, participants also take midazolam, caffeine and bupropion as tablets or oral solution on separate days. Participants are in the study for about 13 months. They visit the study site up to 45 times. At 3 of those visits, participants stay for 5 or 6 days at the study site. During the visits, doctors collect information about participants' health and take blood samples from the participants. They compare the amounts of midazolam, caffeine, and bupropion in the blood in Period 2 with the amounts in Period 1. Doctors also regularly check participants' health and take note of any unwanted effects.

Treatments tested

Main thing measuredArea under the concentration-time curve of bupropion in plasma over the time interval from 0 extrapolated to infinity (AUC 0-∞)
SponsorBoehringer Ingelheim
Conditions studiedOverweight, Obesity
GLP-1 drugs survodutide

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT06564441 ↗