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Study to Evaluate the Safety and Efficacy of X842 in Patients With Reflux Esophagitis

Reflux Esophagitis Clinical Trial

Official title:
A Multicenter, Randomized, Double-blind, Double-simulation, Active Comparator-controlled, Parallel-group Phase II Clinical Study to Evaluate the Efficacy and Safety of X842 Capsules at Different Dosages in Patients With Reflux Esophagitis

Clinical Trial Summary

The purpose of the study is to investigate the efficacy and dose-effect relationship of X842 capsules at different dosages in the treatment of reflux esophagitis for 4 weeks in comparison with lansoprazole enteric-coated capsules.

Clinical Trial Description

It is designed as a multicenter, randomized, double-blind, double-simulation, high and low dose group, active comparator-controlled, parallel-group study to investigate the efficacy and dose-effect relationship of X842 capsules at different dosages in the treatment of reflux esophagitis for 4 weeks in comparison with lansoprazole enteric-coated capsules. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04531475
Study type Interventional
Source Jiangsu Sinorda Biomedicine Co., Ltd
Contact Ming Lu
Phone +8618684676235
Email lum@sinorda.com
Status Recruiting
Phase Phase 2
Start date January 22, 2019
Completion date December 31, 2020
View Details
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