drugset / Trial / NCT02093819

To Assess Safety, Tolerability and Pharmacokinetics of BI 416970 in Healthy Male Volunteers

NCT02093819 ↗

Phase 1 Completed 60 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

To investigate the safety and tolerability of BI 416970 and to assess the pharmacokinetics (PK) of single rising doses of BI 416970. A further objective is to assess the influence of CYP2C9 phenotype on the PK of BI 416970.

Timeline

Start
2014-04
Primary completion
2014-06
Completion
2014-06

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 416970 Unknown — —

Indications

No indication recorded.