The purpose of this study is to evaluate the effect of ADX10059 in patients with gastroesophageal reflux disease who are partial responders to proton pump inhibitors
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
298
Number of GERD symptom free days in week 4 of study medication treatment
Time frame: 4 weeks
GERD symptoms
Time frame: 4 weeks
Sleep disturbance
Time frame: 4 weeks
Use of antacid medications
Time frame: 4 weeks
Global assessment of GERD
Time frame: 4 weeks
Safety and tolerability assessments
Time frame: 4 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
oral administration
Unnamed facility
Little Rock, Arizona, United States
Unnamed facility
Tucson, Arizona, United States
Unnamed facility
Anaheim, California, United States
Unnamed facility
San Diego, California, United States
Unnamed facility
Colorado Springs, Colorado, United States
Unnamed facility
Jacksonville, Florida, United States
Unnamed facility
Port Orange, Florida, United States
Unnamed facility
Moline, Illinois, United States
54
Kansas City, Kansas, United States
62
Kansas City, Kansas, United States
...and 30 more locations