drugset / Trial / NCT04065295

A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225

NCT04065295 ↗

Phase 1 Completed 65 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

The main objectives of the SRD part of this trial are to investigate safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of BI 1356225 in healthy male subjects following oral administration of single rising doses. The main objective of the BA part of this trial will be to explore the influence of food on the bioavailability of tablet fasted versus tablet fed

Timeline

Start
2019-09-09
Primary completion
2019-12-23
Completion
2019-12-23

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1356225 Unknown — Oral

Indications

No indication recorded.