drugset / Trial / NCT03588390

This Study in Healthy Men Tests How Different Doses of BI 1323495 Are Taken up in the Body and How Well They Are Tolerated.

NCT03588390

Phase 1 Completed 63 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

The primary objective of this trial is to investigate the safety and tolerability of BI 1323495 in healthy male subjects following oral administration of single rising doses. Secondary objectives are the exploration of the pharmacokinetics (PK) including dose proportionality and pharmacodynamics (PD) of BI 1323495 after single dosing and the assessment of the PK/PD relationship.

Timeline

Start
2018-07-31
Primary completion
2018-11-14
Completion
2018-11-14

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1323495 Unknown Oral

Indications

No indication recorded.