The objectives of this study are to evaluate the safety, efficacy, and dose-response relationship of IW-3718 administered orally to participants who have GERD and continue to experience GERD symptoms while receiving once-daily (QD), standard-dose proton pump inhibitors (PPIs).
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Percent Change From Baseline to Week 8 in Weekly Heartburn Severity Score (WHSS)
Timeframe: Baseline (derived from the eDiary daily data collected from 7 days before randomization up to the time of randomization), Week 8