Safety, Tolerability and Pharmacodynamic Activity of JNJ-26528398 in Healthy Male Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

November 30, 2011

Primary Completion Date

April 30, 2012

Study Completion Date

April 30, 2012

Conditions
Healthy Participants
Interventions
DRUG

JNJ-26528398

In Study Part 1, the participant will receive an oral solution of JNJ-26528398 3 mg once daily for 7 days. The same dosing regimen is planned for Part 2, but may be adjusted (lower dose and/or fewer dosing days) based on the data from Part 1.

DRUG

Placebo

In both Study Part 1 and Part 2, the participant will receive an oral solution of matching placebo once daily for up to 7 days.

Trial Locations (1)

Unknown

Antwerp

All Listed Sponsors
lead

Janssen Research & Development, LLC

INDUSTRY

NCT01520142 - Safety, Tolerability and Pharmacodynamic Activity of JNJ-26528398 in Healthy Male Participants | Biotech Hunter | Biotech Hunter