drugset / Trial / NCT01398475

A Relative Bioavailability and Food Effect Study of New Formulations

NCT01398475

Phase 1 Completed 15 enrolled Eli Lilly and Company Incyte Corporation · collab
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this trial is to assess the effect of 3 formulations on the relative bioavailability of LY3009104. Participants will receive single dose of LY3009104 on 4 separate occasions with and without food. Safety evaluation and serial pharmacokinetic (PK) samples will be collected during each treatment period. Approximately 5 to 7 days of washout period between each treatment and a follow-up visit will occur approximately 5 to 7 days after the last dose of study drug.

Timeline

Start
2011-07
Primary completion
2011-09
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Baricitinib Small molecule 8 mg Oral

Indications