Humanpharmakologisches Zentrum Biberach
Biberach, 88397, Germany
NCT Number: NCT06655220
The main objective of this trial is to investigate the effect on the exposure of metformin in plasma when administered as an oral multiple dose together with multiple oral doses of BI 1815368 (Test, T) as compared to when metformin is administered as an oral multiple dose alone (Reference, R).
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Notify Me18 year–50 year
Male
Interventional
Phase 1
Biberach, 88397, Germany
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Metformin hydrochloride
BI 1815368
Time frame: Up to 2 days after last dose administration
Time frame: Up to 2 days after last dose administration
Time frame: Up to 2 days after last dose administration
Boehringer Ingelheim
Industry
Investigation of the Effect of BI 1815368 on the Pharmacokinetics of Metformin Following Multiple Oral Administration in Healthy Subjects (an Open-label, Randomised, Two-way Crossover Trial)
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