drugset / Trial / NCT01843972

Safety of Single Rising Doses and Relative Bioavailability of BI 691751

NCT01843972 ↗

Phase 1 Completed 81 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

To investigate safety, tolerability, pharmacokinetics (PK), and pharmacodynamics of single rising doses of BI 691751 in healthy male subjects (part I). To investigate the relative bioavailability of BI 691751 given as tablet versus oral solution (part II)

Timeline

Start
2013-04
Primary completion
2013-11
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 691751 Unknown — Oral

Indications

No indication recorded.