Viewing Study NCT01161602



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Last Modification Date: 2024-10-26 @ 10:22 AM
Study NCT ID: NCT01161602
Status: COMPLETED
Last Update Posted: 2011-09-21
First Post: 2010-07-12

Brief Title: A Study to Evaluate the Safety Tolerability and Pharmacodynamics of Pumosetrag in Patients With Gastroesophageal Reflux Disease GERD
Sponsor: Edusa Pharmaceuticals Inc
Organization: Edusa Pharmaceuticals Inc

Study Overview

Official Title: A Phase IIa Randomized Double-Blind Placebo-Controlled Study to Evaluate the Safety Tolerability and Pharmacodynamics of Multiple Dose Levels of Pumosetrag in Patients With Symptoms Associated With Gastroesophageal Reflux Disease GERD Receiving a Standard Refluxogenic Meal
Status: COMPLETED
Status Verified Date: 2011-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine if pumosetrag is effective in treating Gastroesophageal Reflux Disease GERD symptoms in patients who have a history of GERD symptoms and are currently taking an acid suppression therapy such as a Proton Pump Inhibitor PPI
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None