A Study to Evaluate Single and Repeat Doses of IV GSK2251052 in Healthy Male Japanese and Caucasian Subjects and Repeat Doses of Supratherapeutic Doses of IV GSK2251052 in Healthy Volunteers

PHASE1TerminatedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

December 19, 2011

Primary Completion Date

February 17, 2012

Study Completion Date

February 17, 2012

Conditions
Community-acquired Infection
Interventions
DRUG

GSK2251052 750 mg

Treatment A: 750 mg IV GSK2251052 single dose

DRUG

GSK2251052 1500 mg

Treatment B: 1500 mg IV GSK2251052 single dose

DRUG

GSK2251052 1500 mg BID

Treatment C: 1500 mg IV GSK2251052 BID or placebo for 12 days

DRUG

GSK2251052 2250 mg

Treatment D: On Day 1 a single dose of GSK2251052 2250 mg IV administered over 60 minutes; Days 4 - 12 BID doses of GSK2251052 2250 mg IV (for 9 days), fasted

DRUG

GSK2251052 3000 mg

Treatment E: On Day 1 a single dose of GSK2251052 3000 mg IV administered over 60 minutes; Days 4 - 12 BID doses of GSK2251052 3000mg IV (for 9 days), fasted

DRUG

GSK2251052 0.9% saline

Treatment P: On Day 1 a single dose of 0.9% saline IV administered over 60 minutes; On Days 4 - 12 BID doses of 0.9% saline (for 9 days), fasted

Trial Locations (1)

91206

GSK Investigational Site, Glendale

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT01495065 - A Study to Evaluate Single and Repeat Doses of IV GSK2251052 in Healthy Male Japanese and Caucasian Subjects and Repeat Doses of Supratherapeutic Doses of IV GSK2251052 in Healthy Volunteers | Biotech Hunter | Biotech Hunter