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Assessment of the Effects of Zegerid Powder for Oral Suspension 40 mg on 24-Hour and Nocturnal Esophageal Acid Exposure in Patients With Gastroesophageal Reflux Disease and Barrett's Esophagus.

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Trial Profile

Assessment of the Effects of Zegerid Powder for Oral Suspension 40 mg on 24-Hour and Nocturnal Esophageal Acid Exposure in Patients With Gastroesophageal Reflux Disease and Barrett's Esophagus.

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 08 Jun 2017

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At a glance

Most Recent Events

  • 02 Jun 2017 Status changed from recruiting to discontinued.
  • 01 Jun 2010 New trial record

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