Overview

GSK2251052 Mass Balance in Healthy Adult Subjects

Status:
Completed
Trial end date:
2011-05-19
Target enrollment:
Participant gender:
Summary
Approximately 6 healthy male subjects will be administered a single 1500 mg intravenous dose of 14C-GSK2251052 under fasted conditions. Blood, urine and fecal samples will be collected for a minimum of 14 days following study drug administration. Safety and tolerability will be monitored throughout the study. A follow-up visit will occur 7-14 days after study drug administration.
Phase:
Phase 1
Details
Lead Sponsor:
GlaxoSmithKline