drugset / Trial / NCT02259972

Safety, Tolerability and Pharmacokinetics of Single Rising Oral Doses of BI 113823 Powder in Bottle (PiB) and Tablet in Healthy Male Volunteers

NCT02259972

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

Summary

To investigate the safety, tolerability, and pharmacokinetics incl. dose proportionality of BI 113823, as well as the relative bioavailability of PiB vs. tablet and tablet fasted vs. fed (food effect for the tablet).

Timeline

Start
2010-01
Primary completion
2010-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 113823 Unknown 5 mg Oral
Subject BI 113823 Unknown 800 mg Oral

Indications

No indication recorded.