A Study to Investigate the Safety Tolerability Pharmacokinetics, and Pharmacodynamics of Inhaled and Intravenous GSK2862277 in Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

54

Participants

Timeline

Start Date

February 22, 2013

Primary Completion Date

October 25, 2013

Study Completion Date

October 25, 2013

Conditions
Respiratory Disorders
Interventions
DRUG

Single IV dose of GSK2862277

GSK2862277 solution available in a 40 mg vial for IV administration.

DRUG

Matching placebo single dose IV infusion

Matching placebo solution available for IV administration.

DRUG

Single IH dose of GSK2862277

GSK2862277 nebulised solution available in a 40 mg vial for IH administration.

DRUG

Matching placebo single dose IH

Matching placebo nebulised solution available for IH administration.

DRUG

Repeat IV dose of GSK2862277

GSK2862277 solution available in a 40 mg vial for IV administration.

DRUG

Matching placebo repeat dose IV infusion

Matching placebo solution available for IV administration.

DRUG

Repeat IH dose selected of GSK2862277 from Part 2

GSK2862277 nebulised solution available in a 40 mg vial for IH administration.

DRUG

Matching placebo repeat dose IH

Matching placebo nebulised solution available for IH administration.

Trial Locations (1)

HA13UJ

GSK Investigational Site, Harrow

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT01818024 - A Study to Investigate the Safety Tolerability Pharmacokinetics, and Pharmacodynamics of Inhaled and Intravenous GSK2862277 in Healthy Volunteers | Biotech Hunter | Biotech Hunter