A Study to Evaluate Safety, Tolerability and Pharmacokinetics of Ascending Intravenous Single Dose and Repeat Dose of GSK3342830

PHASE1TerminatedINTERVENTIONAL
Enrollment

62

Participants

Timeline

Start Date

June 13, 2016

Primary Completion Date

February 2, 2017

Study Completion Date

February 2, 2017

Conditions
Infections, Bacterial
Interventions
DRUG

GSK3342830

A pyrogen free lyophilized formulation, white to yellowish brown powder containing 1000 mg of GSK3342830A (as free base) per vial. The reconstituted solution looks like a clear, colorless to yellow or brownish yellow liquid, free from visible particulate matter will be administered as IV infusion over 1 hour.

DRUG

Placebo

A clear and colorless solution containing 0.9% sodium chloride. It will administered as IV infusion over 1 hour.

Trial Locations (1)

5000

GSK Investigational Site, Adelaide

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY