A Relative Bioavailability Study of Fluticasone Furoate and Levocabastine

PHASE1CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

October 11, 2013

Primary Completion Date

February 27, 2014

Study Completion Date

February 27, 2014

Conditions
Rhinitis, Allergic, Perennial and Seasonal
Interventions
DRUG

FF/LEV FDC

Intranasal aqueous microsuspension containing 25.0 microgram (µg) of FF and 50 µg of LEV as a fixed dose combination. It will be administered as two 50 µL sprays per nostril in the morning in a fasted state

DRUG

FF

Intranasal aqueous microsuspension containing 27.5µg of FF. It will be administered as two 50 µL sprays per nostril in the morning in a fasted state

DRUG

LEV

Intranasal aqueous microsuspension containing 50 µg of LEV. It will be administered as two 50 µL sprays per nostril in the morning in a fasted state

Trial Locations (1)

2031

GSK Investigational Site, Randwick

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY