A Phase 1 (Ph1), Single Dose (SD), GSK961081 Absorption, Distribution, Metabolism, and Excretion (ADME) Study in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

February 8, 2016

Primary Completion Date

March 17, 2016

Study Completion Date

March 17, 2016

Conditions
Pulmonary Disease, Chronic Obstructive
Interventions
DRUG

[14C]-GSK961081 solution for IV infusion

Subjects will receive 10 mL of solution equivalent to 4 mcg of \[14C\]-GSK961081 (approximately 6.2 kilobecquerel \[kBq\]) intravenously as a single dose over 1 hour.

DRUG

[14C]-GSK961081 oral solution

Subjects will receive 10 mL of solution equivalent to 200 mcg of \[14C\]-GSK961081 (approximately 311 kBq) orally as a single dose with up to 250 mL of water.

DRUG

GSK961081 dry powder for inhalation

Subjects will receive single dose of 4 actuations of 300 mcg GSK961081 per actuation (1200 mcg GSK961081 total) as inhalation immediately after the start of infusion.

Trial Locations (1)

NW10 7EW

GSK Investigational Site, London

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Hammersmith Medicines Research

OTHER

collaborator

GlaxoSmithKline

INDUSTRY

lead

Theravance Biopharma

INDUSTRY