A Trial of IW-3718 for 8 Weeks in Patients With Symptomatic

Clinical Trial Summary

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).

See also
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NCT number	NCT02637557
Study type	Interventional
Source	Ironwood Pharmaceuticals, Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	March 1, 2016
Completion date	April 26, 2017

A Trial of IW-3718 for 8 Weeks in Patients With Symptomatic Gastroesophageal Reflux Disease (GERD)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms