A Study to Assess the Relative Oral Bioavailability of a Single Dose of JNJ-63623872/Oseltamivir Fixed-dose Combination Tablet and Single Agent Concept Formulations of JNJ-63623872 Compared to Their Respective Reference Formulation in Healthy Adult Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

45

Participants

Timeline

Start Date

February 14, 2017

Primary Completion Date

April 14, 2017

Study Completion Date

April 14, 2017

Conditions
Healthy
Interventions
DRUG

JNJ-63623872

Participants will receive JNJ-63623872 600 mg (2\*300 mg) oral tablets in Panel 1 and 2 under Fasted conditions.

DRUG

Oseltamivir

Participants will receive Oseltamivir 75 mg (1\*75 mg) oral capsule (reference) in Treatment D of Panel 2 and Oseltamivir 75 mg administered as JNJ-63623872/37.5 mg Oseltamivir oral FDC tablet concept formulation (test 3) in Treatment E of Panel 2.

Trial Locations (1)

2060

SGS Life Science Services, Antwerp

Sponsors
All Listed Sponsors
lead

Janssen-Cilag International NV

INDUSTRY