drugset / Trial / NCT01146886

Trial to Investigate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Oral Doses of BI135585 XX Administered as Tablet and as Solution in Healthy Volunteers

NCT01146886 ↗

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

Summary

The purpose of the study is to investigate the safety, tolerability, pharmacokinetics incl. dose proportionality, and pharmacodynamics of BI 135585 XX (Part 1), as well as the relative bioavailability of two different immediate release tablet formulations versus oral solution (Part 2)

Timeline

Start
2010-06
Primary completion
2010-09
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 135585 Unknown 200 mg Oral