drugset / Trial / NCT02205112

A Phase III Study to Evaluate the Efficacy and Safety of Intravenous Infusion of Nemonoxacin in Treating CAP

NCT02205112

Phase 3 Completed 598 enrolled TaiGen Biotechnology Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy, safety and pharmacokinetics of intravenous nemonoxacin compared with intravenous moxifloxacin in adult patients with community-acquired pneumonia (CAP).

Timeline

Start
2014-06
Primary completion
2017-05-04
Completion
2017-05-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Levofloxacin Small molecule 500 mg Intravenous
Subject Nemonoxacin Small molecule 500 mg Intravenous

Indications