An Investigation of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GSK2245035 in Healthy Volunteers and Allergic Rhinitics.

PHASE1CompletedINTERVENTIONAL
Enrollment

61

Participants

Timeline

Start Date

May 30, 2011

Primary Completion Date

September 30, 2011

Study Completion Date

September 30, 2011

Conditions
Rhinitis, Allergic, Seasonal
Interventions
DRUG

2 ng GSK2445053

2ng GSK2445053 administered intranasally

DRUG

20ng GSK2445053

20ng GSK2445053 administered intranasally

DRUG

100ng GSK2445053

100ng GSK2445053 administered intranasally

DRUG

200ng GSK2445053

200ng GSK2445053 administered intranasally

DRUG

400ng GSK2445053

400ng GSK2445053 administered intranasally

DRUG

1000ng GSK2445053

1000ng GSK2445053 administered intranasally

DRUG

2000ng GSK2445053

2000ng GSK2445053 administered intranasally

DRUG

4000ng GSK2445053

4000ng GSK2445053 administered intranasally

DRUG

Placebo

Placebo administered intranasally

Trial Locations (1)

9471 GP

GSK Investigational Site, Zuidlaren

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT01480271 - An Investigation of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GSK2245035 in Healthy Volunteers and Allergic Rhinitics. | Biotech Hunter | Biotech Hunter