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Clinical Trial Summary

A randomized, double-blind, double-dummy, active comparator, multi-centers, non-inferiority design clinical trial to assess the efficacy and safety of YYD601 in ERD patients (phase 3).


Clinical Trial Description

This phase 3 clinical trial is designed as randomized, active-comparator, double-dummy, multi-center for ERD patients, who take YYD601 40mg or Nexium 40mg for 8 weeks. Each part is assessed by 'LA grade' measured through the endoscopy, target goal is to confirm the non-inferiority of YYD601 40mg to Nexium 40mg. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03943992
Study type Interventional
Source Yooyoung Pharmaceutical Co., Ltd.
Contact
Status Completed
Phase Phase 3
Start date January 29, 2019
Completion date July 1, 2020

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