Rabeprazole Extended-Release 50 mg Versus Esomeprazole 40 mg for Healing and Symptomatic Relief of Mild to Moderate Erosive Gastroesophageal Reflux Disease (GERD)
Status: | Completed |
---|---|
Conditions: | Gastroesophageal Reflux Disease |
Therapuetic Areas: | Gastroenterology |
Healthy: | No |
Age Range: | 18 - 75 |
Updated: | 4/21/2016 |
Start Date: | February 2008 |
End Date: | September 2009 |
A Randomized Double-Blind Parallel Study of Rabeprazole Extended-Release 50 mg Versus Esomeprazole 40 mg for Healing and Symptomatic Relief of Mild to Moderate Erosive Gastroesophageal Reflux Disease (GERD)
The purpose of this study is to investigate the efficacy and safety of Rabeprazole (RAB)
Extended-Release (ER) 50 mg versus Esomeprazole (ESO) 40 mg in subjects with erosive
gastroesophageal reflux disease (eGERD).
Extended-Release (ER) 50 mg versus Esomeprazole (ESO) 40 mg in subjects with erosive
gastroesophageal reflux disease (eGERD).
This is a multicenter, randomized, double-blind, double-dummy, parallel-group study.
Subjects who meet all the inclusion/exclusion criteria will be randomly assigned to 1 of 2
treatment groups, Rabeprazole Extended-Release (RAB ER) 50 mg or Esomeprazole (ESO) 40 mg
for the treatment of mild to moderate erosive Gastroesophageal Reflux Disease (GERD).
Subjects who meet all the inclusion/exclusion criteria will be randomly assigned to 1 of 2
treatment groups, Rabeprazole Extended-Release (RAB ER) 50 mg or Esomeprazole (ESO) 40 mg
for the treatment of mild to moderate erosive Gastroesophageal Reflux Disease (GERD).
KEY INCLUSION CRITERIA:
1. Male or female, ages 18 to 75 years.
2. History of gastroesophageal reflux disease (GERD) symptoms for at least 3 months
immediately before screening.
3. Heartburn for at least 2 days a week for at least 1 month before screening.
4. Esophageal erosions of Los Angeles (LA) Grades A or B based on EGD taken within 14
days prior to enrollment.
5. Subjects who are H. pylori negative based on a screening test.
6. Females should be either of non-childbearing potential or of childbearing potential.
Females of childbearing potential must have negative pregnancy tests prior to
randomization. Female subjects of childbearing potential must agree to use medically
acceptable methods of contraception.
7. Subjects must be able to read, write, and understand the language of the symptom
diary.
KEY EXCLUSION CRITERIA:
1. Current or a history of esophageal motility disorders.
2. Current or a history of Barrett's esophagus. Current esophageal strictures or
esophagitis (known or suspected to be due to etiology other than GERD such as
infection or medications).
3. Current or a history of Zollinger-Ellison syndrome and other acid hypersecretory
conditions, or current gastric or duodenal ulcer.
4. Current or a history of cancer, with the exception of fully excised skin basal cell
carcinoma.
5. Inflammatory bowel disease.
6. Unstable diabetes mellitus.
7. History of esophageal, gastric and duodenal surgery except simple suturing of an
ulcer.
8. Subjects who require daily use of nonsteroidal anti-inflammatory drugs (NSAIDs), oral
steroids (>=20 mg/day prednisone or equivalent), or aspirin (> 325 mg/day).
We found this trial at
76
sites
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