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Observationa Study is a Prospective and Multi-institutional Observational Study.

Jeil Pharmaceutical logo

Jeil Pharmaceutical

Status

Completed

Conditions

Heartburn
Erosive Reflux Disease
Acid Regurgitation

Study type

Observational

Funder types

Industry

Identifiers

NCT06952855
JL-JAQ-401

Details and patient eligibility

About

This observational study is a prospective, multi-institutional non intervention study to examine the prescription patterns, corresponding treatment effects and safety in routine clinical practice for patients prescribed for the treatment of gastroesophageal reflux disease.

Full description

The present observational study is designed to check effect and safety for patients who have been prescribed JAQBO for the treatment of erosive gastroesophageal reflux disease.

Enrollment

5,536 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. An adult over 19 years of age
  2. A person who voluntarily provides written informed consent

Exclusion criteria

  1. A pregnant woman or a nursing woman
  2. A person who is deemed unsuitable for the subject of the study

Trial design

5,536 participants in 1 patient group

1 cohort
Description:
No interventions

Trial contacts and locations

1

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Central trial contact

DOH YEON Manager; JAE WON Manager

Data sourced from clinicaltrials.gov

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