drugset / Trial / NCT02265640

Relative Bioavailability, Pharmacokinetics, Safety and Tolerability of BIIL 284 BS in Healthy Volunteers

NCT02265640

Phase 1 Completed 16 enrolled Boehringer Ingelheim
RandomizedCrossoverOpen-labelTreatment

Summary

The objective of the present study is to investigate the relative bioavailability of BIIL 284 BS boli in comparison to the tablet C at a dose of 75 mg in fasted condition and after a standard breakfast in healthy male volunteers

Timeline

Start
2000-10
Primary completion
2000-12
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject AMELUBANT Small molecule 75 mg

Indications

No indication recorded.