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Clinical Trials · NCT06200467

A Study to Test Whether Multiple Doses of BI 456906 Have an Effect on Cardiac Safety in People With Overweight or Obesity

CompletedPhase 1Survodutide (Approved)
Phase
Phase 1
Recruitment status
Completed
Sponsor
Boehringer Ingelheim
Enrollment
110
Start date
Mar 2024
Locations
1 site, Germany
Primary endpoint
Time-matched QTcI change from baseline (ΔQTcI) collected at the same time points as the BI 456906 plasma concentrations up to a maximum of 30 weeks after first drug administration of BI 456906 / BI 456906-placebo
View Survodutide compound reference