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A Study Evaluating Efficacy and Safety of CRO-SBT in the Treatment of Gonorrhea — CRO-SBT  

Gonorrhea Clinical Trial

Official title:
A Study Evaluating Efficacy and Safety of Ceftriaxone Sodium and Sulbactam Sodium for Injection in the Treatment of Uncomplicated Urogenital Gonorrhea

Clinical Trial Summary

This is a phaseIV, multicenter, open-label，single arm study which will be performed to evaluate efficacy and safety of Ceftriaxone sodium and Sulbactam Sodium for injection for the treatment of uncomplicated urogenital infection caused by Neisseria gonorrhoeae in adolescent and adult subjects.

Clinical Trial Description

In this study, adults will be administered as one 3g IV dose at the study site,Children under 12 will be administered as one 75mg/kg IV dose . Approximately 100 subjects will be recruited to receive study treatment. The duration of the study will be approximately 14 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04202068
Study type Interventional
Source Xiangbei Welman Pharmaceutical Co., Ltd
Contact
Status Completed
Phase Phase 4
Start date July 3, 2015
Completion date May 30, 2016
View Details
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