drugset / Trial / NCT02202187

A Single Oral Escalating Dose Study of GSK2140944 in Healthy Volunteers

NCT02202187

Phase 1 Completed 48 enrolled GlaxoSmithKline
RandomizedParallel-groupSingle-blindOther

Summary

GSK2140944 belongs to the Bacterial Type II Topoisomerase Inhibitor (BTI) class of antibiotics. GSK2140944 has demonstrated in vitro and in vivo activity against Gram positive including methicillin resistant Staphylococcus aureus (MRSA) and Gram-negative pathogens associated with respiratory tract, skin and soft tissue infections including isolates resistant to existing classes of antimicrobials. This is a First Time in Human (FTIH) study to assess the safety, tolerability, and pharmacokinetics of single oral doses of GSK2140944 in healthy volunteers. This study will be a single-blind, randomized, placebo-controlled, dose-rising study in healthy subjects. The proposed single doses will range from 100 mg to 3000 mg.

Timeline

Start
2011-09-26
Primary completion
2012-02-15
Completion
2012-02-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Gepotidacin Small molecule 100 mg Oral
Subject Gepotidacin Small molecule 3000 mg Oral