|Clinical Trial Title||RECLAIM|
|Trial Status||Open to Enrollment|
The objective of this study is to evaluate the safety and efficacy of IW-3718 administered to patients with GERD who continue to have persistent symptoms, such as heartburn and regurgitation, while receiving once-daily (QD), standard-dose proton pump inhibitors (PPIs).
Experimental: Three 500 mg study drug tablets administered twice daily (BID), immediately after the morning and evening meals.
Placebo Comparator: Three placebo tablets administered BID immediately after the morning and evening meals.
Ages Eligible for Study: 18 years and older
Each patient must meet all of the following criteria to be eligible for enrollment in this study:
Patients who meet any of the following criteria will not be eligible to participate in the study:
NOTE: Other inclusion and exclusion criteria apply, per the study protocol.
|Principal Investigator||Harald Schoeppner, MD|
|Contact Name||Paul Fitzpatrick|