Skip to main content
OpenTrials
Completed

NCT Number: NCT03967886

Clinical Trial to Assess the Efficacy and Safety of YYD601 in NERD Patients

Clinical Trial to Assess the Efficacy and Safety of YYD601 in NERD Patients

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Korea University Ansan Hospital

Seoul, South Korea

About this study

This Phase 3 Clinical Trial is Designed as Randomized, Double-blind, Placebo-controlled, Multi-centers Clinical Trial to Assess the Efficacy and Safety of YYD601 in NERD Patients (Phase3).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • A man or woman over 20 years old less than 70 years old.
  • A man or woman who has below all characters and diagnosis as NERD.
  • A man or woman who has experienced symptom(hearburn or/and acid regurgitation) over 3month at least.
  • A man or woman who has experienced symptom(heartburn or/and acid regurgitation) within 7days before Visit1, meet below 1) or 2) criteria.

** Symptom (heartburn and acid regurgitation) is confirmed by RDQ

  • Experienced above 2 days in a week, heartburn of acid regurgitation above the weakness.
  • Experienced above 1 day in a week, heartburn of acid regurgitation above the middle.
  • A man or woman who has been made diagnosis as LA grade0(Zero) measured through the dendoscopy which is corried out within 14 days, there is no observed muscosal break.
  • A man or woman who has a full understanding of this clinical trial through the detailed explanation, agree in writing to participate in this trial.

Exclusion criteria

  • Who has hyper sensitivity reaction about other drugs, ingredients, components of investigator product or compound of benzimidazole.
  • Who has ERD.
  • Who get a diagnosis as a IBS within the last 3 months.
  • Who have taken drugs about reflux esophagitis (H₂-receptor inhibitor (H2RA) Prostaglandin(PG), Antacid, Prokinetic acid etc.) above 2 times as an usual dose. (* refer to the Concomitant medication in text.)
  • Who havbe taken gastric acid secretion inhibitors including PPIs within 2 weeks before the endoscopy.
  • Who has been experienced the disease affecting the esophagus(Eosinophilic esophagitis, esophageal varices, cirrhosis, Virus or Fungal infection, Esophageal stricture, primary esophageal motility disorder and gastrointestinal bleeding). Or who has a history of radio therapeutics, freeze treatment about the esophagus.
  • Who has the gastric or duodenal ulcer, Zollinger-Ellison and other acid hypersecretory condition been experienced.
  • Who has hyper-sensitivity, reaction about PPIs (ex. Lansoprazole, omeprazole, rabeprazole, pantoprazole or esomeprazole).
  • Who has gotten a diagnosis as a cancer within 5 years before participated in this clinical trail (expect the basal cell on the skin), peptic ulcer or benign tumor.

Treatment and study plan

YYD601 20mg

Drug

Patients should take drugs an hour before breakfast.

Nexium 20mg

Drug

Patients should take drugs an hour before breakfast.

Placebos

Drug

The placebo YYD601 is made from microcrystalline cellulose covered with hard shell. The placebo Nexium is made from microcrystalline cellulose, Crospovidone, Magnesiumstearat and other ingredients.

Primary outcomes

  1. Recovered percentage(%) of the symptom

    Time frame: within 4 weeks

    Recovered percentage(%) of the symptom(heartburn or/and acid regurgitation) measured by RDQ after administration(baseline).

  2. Change of the score about the symptom

    Time frame: within 4 weeks

    Change of the score about the symptom(heartburn or/and acid regurgitation) measured by RDQ after administration(baseline).

  3. Percentage(%) of the patients who have symptom during the daytime

    Time frame: within 4 weeks

    Percentage(%) of the patients who have symptom(heartburn or/and acid regurgitation) during the daytime measured by Patients diary after administration(baseline).

  4. Percentage(%) of the patients who have symptom during the nighttime

    Time frame: within 4 weeks

    Percentage(%) of the patients who have symptom(heartburn or/and acid regurgitation) during the nighttime measured by Patients diary after administration(baseline).

  5. Percentage(%) of the days no symtom

    Time frame: within 4 weeks

    Percentage(%) of the days no symptom(heartburn or/and acid regurgitation) among the patients who have symptom(heartburn or/and acid regurgitation) during the nighttime measured by Patients diary after administration(baseline).

Sponsors and collaborators

Lead sponsor

Yooyoung Pharmaceutical Co., Ltd.

Industry

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled, Multi-centers Clinical Trial to Assess the Efficacy and Safety of YYD601 in NERD Patients (Phase3).

Important dates

Study start
2019
Primary completion
2019
Study completion
2020
First posted
May 30, 2019
Registry last updated
May 11, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.