drugset / Trial / NCT01211964

LEO 22811 - Single Dose Bioavailability Study of Tablet Versus Oral Solution in Healthy Subjects

NCT01211964 ↗

Phase 1 Completed 15 enrolled LEO Pharma
RandomizedCrossoverOpen-labelOther

Summary

The purpose of this phase 1 study is to determine the relative bioavailability and pharmacokinetics following single oral dose administration of LEO 22811 solution compared to LEO 22811 tablet in healthy male subjects as well as to determine the effect of food on the single oral dose pharmacokinetics of LEO 22811 tablet in healthy male subjects.

Timeline

Start
2010-09
Primary completion
2010-12
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject LEO 22811 Unknown 1.5 mg Oral

Indications

No indication recorded.