drugset / Trial / NCT02733627

To Investigate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BI 1467335 Following Multiple Dose Administration Over 28 Days

NCT02733627

Phase 1 Completed 36 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this trial is to investigate the safety and tolerability of BI 1467335 in healthy male and female subjects following oral administration of multiple rising doses over 28 days. Secondary objectives are the exploration of the pharmacokinetics (PK) and target engagement biomarkers of BI 1467335 after multiple dosing.

Timeline

Start
2016-07-07
Primary completion
2017-07-12
Completion
2017-07-12

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1467335 Unknown 10 mg Oral
Subject BI 1467335 Unknown 15 mg Oral
Subject BI 1467335 Unknown 20 mg Oral

Indications

No indication recorded.