Clinical Trial to Evaluate the Safety and Efficacy of JP-1366 in Patients With Erosive Gastroesophageal Reflux Disease

  • STATUS
    Recruiting
  • participants needed
    200
  • sponsor
    Jeil Pharmaceutical Co., Ltd.
Updated on 19 February 2024
endoscopy
esophagogastroduodenoscopy
esomeprazole
reflux
heartburn
acidity
esomeprazole 40 mg
acid reflux / gastroesophageal reflux

Summary

Clinical trial to evaluate the safety and efficacy of JP-1366 in patients with erosive gastroesophageal reflux disease

Details
Condition Gastroesophageal Reflux
Age 19-75 years
Treatment JP-1366, JP-1366 placebo, Esomeprazole 40mg, Esomeprazole placebo
Clinical Study IdentifierNCT04282954
SponsorJeil Pharmaceutical Co., Ltd.
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Adults between 19 and 75 years old based on the date of written agreement
Those who have been diagnosed with erosive gastroesophageal reflux disease(EGRD) of LA Grade A-D on the upper gastrointestinal endoscopy
Those who experienced symptoms of heartburn or acid reflux within the last 7 days

Exclusion Criteria

Those who have undergone gastric acid suppression or gastric, esophageal surgery
Those who with clinically significant liver, kidney, nervous system, respiratory, endocrine, hematologic, cardiovascular, urinary system disease
Clinically significant abnormal laboratory values during screening
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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