drugset / Trial / NCT01662661

A Study to Compare the Bioavailability of JNJ-47910382 Formulated as a Tablet and as Suspension in Healthy Participants

NCT01662661 ↗

Phase 1 Completed 14 enrolled Janssen R&D Ireland
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to assess the relative bioavailability (the degree to which the study medication becomes available in the blood circulation) of JNJ-47910382, given as an uncoated tablet and as a suspension, after a single oral dose of 200 mg in healthy adult participants under fed conditions.

Timeline

Start
2012-07
Primary completion
2012-08
Completion
2012-09

Drugs

EvaluationDrugModalityDoseRoute
Subject JNJ-47910382 Unknown 200 mg Oral

Indications

No indication recorded.