A Study to Evaluate the Bioavailability, Safety and Tolerability of a Solid Dosage Formulation Relative to a Suspension of JNJ-54175446 in Healthy Male and Female Participants

2016-10-13 01:38:27 | BioPortfolio


The primary purpose of the study is to investigate the plasma pharmacokinetics and bioavailability (BA) of a single dose of a solid dose formulation with 2 different strengths of JNJ-54175446 (50 milligram [mg] and 100 mg capsules) relative to the suspension of JNJ-54175446 under fasting conditions.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label




JNJ-54175446 (capsule), JNJ-54175446 (suspension)


Overland Park
United States


Not yet recruiting


Janssen Research & Development, LLC

Results (where available)

View Results


Published on BioPortfolio: 2016-10-13T01:38:27-0400

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