A Study to Evaluate the Effect of Lansoprazole on Infants With Gastroesophageal Reflux Disease.
Gastroesophageal Reflux Disease
About this trial
This is an interventional treatment trial for Gastroesophageal Reflux Disease focused on measuring Pediatric GERD, Pediatric Gastroesophageal Reflux Disease, lansoprazole
Eligibility Criteria
Inclusion Criteria: Hospitalized or outpatient male or female, term or post-term infants beyond the neonatal period (>28 days) but less than 12 months of age, OR a preterm infant with a corrected age of at least 44 weeks but less than 12 months on Dosing Day 1. Clinically-evident Gastroesophageal Reflux Disease (feeding intolerance, regurgitation, wheezing or stridor with feedings) At least 7 days post-surgery without anticipated need for surgery during study No significant laboratory abnormalities Exclusion Criteria: Unstable, clinically significant disease or abnormality Congenital anomaly of the upper gastrointestinal tract Clinical evidence of acute sepsis Cystic fibrosis Medical condition requiring subject to not be fed by mouth/gastric tube
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Lansoprazole 1.0 mg/kg QD
Lansoprazole 2.0 mg/kg QD