A Study to Investigate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of JNJ-42847922 in Healthy Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

May 31, 2014

Primary Completion Date

November 30, 2014

Study Completion Date

November 30, 2014

Conditions
Healthy
Interventions
DRUG

JNJ-42847922 5 mg

Participants will receive 5 mg of JNJ-42847922, from Day 1 up to Day 10.

DRUG

JNJ-42847922 10 mg

Participants will receive 10 mg of JNJ-42847922, from Day 1 up to Day 10.

DRUG

JNJ-42847922 20 mg

Participants will receive 20 mg of JNJ-42847922, from Day 1 up to Day 10.

DRUG

JNJ-42847922 40 mg

Participants will receive 40 mg of JNJ-42847922, from Day 1 up to Day 10 .

DRUG

Placebo

Participants will receive matching placebo from Day 1 up to Day 10.

Trial Locations (1)

Unknown

Berlin

Sponsors
All Listed Sponsors
lead

Janssen-Cilag International NV

INDUSTRY