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Clinical Trials · NCT05421338

A Study in Healthy Men to Test How BI 456906 is Processed in the Body

CompletedPhase 1Survodutide (Approved)
Phase
Phase 1
Recruitment status
Completed
Sponsor
Boehringer Ingelheim
Enrollment
6
Start date
Jul 2022
Locations
1 site, Netherlands
Primary endpoint
Fraction of [14C]-radioactivity excreted in urine expressed as percentage of the administered dose over the time interval from 0 to the last quantifiable time point (fe_urine, 0-tz)
View Survodutide compound reference