18
Participants
Start Date
November 30, 2016
Primary Completion Date
December 31, 2016
Study Completion Date
December 31, 2016
Placebo
0.9% weight by volume (w/v) saline solution for intravenous infusion over 1 hour (in Cohort 1) or over 15 hours (in Cohort 2).
GSK2315698
200 mg/mL stock solution for intravenous infusion over 1 hour (in Cohort 1) or over 15 hours (in Cohort 2). The stock solution will be diluted to obtain dosage levels of 10 mg/hr, 20 mg/hr, or 40 mg/hr.
GSK Investigational Site, Tokyo
Lead Sponsor
GlaxoSmithKline
INDUSTRY