drugset / Trial / NCT02173665

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Oral Doses of BI 1356 BS Administered to Healthy Male Subjects

NCT02173665 ↗

Phase 1 Completed 64 enrolled Boehringer Ingelheim
RandomizedSingle-groupDouble-blindTreatment

Summary

The objective of the current study was to investigate safety, tolerability, pharmacokinetics and pharmacodynamics of BI 1356 BS.

Timeline

Start
2004-10
Primary completion
2004-12
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Linagliptin Unknown 2.5 mg Oral
Subject Linagliptin Unknown 5 mg Oral
Subject Linagliptin Unknown 25 mg Oral
Subject Linagliptin Unknown 600 mg Oral

Indications

No indication recorded.