Symptom improvements in Gastroesophageal reflux disease (GERD) patients

Study identifier:D9120C00011

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A randomized, double-blind, placebo controlled, phase IIA study to assess the effect on Gastroesophageal reflux disease (GERD) symptoms, Pharmacokinetics, safety and tolerability of 4 weeks treatment with AZD3355 65 mg bid as add-on treatment to a Proton pump inhibitor (PPI) in patients with an incomplete response to PPI.

Medical condition

Gastroesophageal reflux disease (GERD)

Phase

Phase 2

Healthy volunteers

No

Study drug

AZD3355

Sex

All

Actual Enrollment

244

Study type

Interventional

Age

17 Years - 70 Years

Date

Study Start Date: 01 Nov 2006
Primary Completion Date: 01 Jun 2007
Study Completion Date: 01 Jun 2007

Study design

Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment

Verification:

Verified 01 Feb 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria