drugset / Trial / NCT02244827

Pharmacokinetics of WCK 2349 In Patients With Hepatic Impairment

NCT02244827

Phase 1 Completed 48 enrolled Wockhardt
NaSingle-groupOpen-labelBasic science

Summary

This study is aimed to compare the pharmacokinetics of levonadifloxacin and its sulfate metabolite after a single dose of oral WCK 2349 1000 mg in patients with hepatic impairment and healthy volunteers.

Timeline

Start
2014-09
Primary completion
2014-12
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Levonadifloxacin Small molecule 1000 mg Oral