Viewing Study NCT00730665



Ignite Creation Date: 2024-05-05 @ 7:45 PM
Last Modification Date: 2024-10-26 @ 9:53 AM
Study NCT ID: NCT00730665
Status: TERMINATED
Last Update Posted: 2011-07-14
First Post: 2008-08-06

Brief Title: Efficacy And Safety Of PF-00885706 For The Relief Of Symptoms In Subjects With Gastro-esophageal Reflux Disease GERD
Sponsor: Pfizer
Organization: Pfizer

Study Overview

Official Title: A Parallel-Group Randomized Double-Blind Multi-Center Dose Response Study To Evaluate The Efficacy And Safety Of PF-00885706 A 5-HT4 Receptor Partial Agonist As Add-On Therapy To Esomeprazole For The Relief Of Symptoms In Subjects With Gastro-esophageal Reflux Disease GERD Who Have A Poor Response To Proton Pump Inhibitor PPI Treatment
Status: TERMINATED
Status Verified Date: 2011-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: This study has been placed on clinical hold by the sponsor due to operational reasons
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To understand the dose-response characteristics of PF-00885706 for efficacy in terms of symptomatic relief when used as add-on treatment to esomeprazole 20mg standard proton pump inhibitor PPI treatment in subjects with gastro-esophageal reflux GERD who have inadequate relief with PPIs
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