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Completed Phase 2 Interventional Results available

Safety and Efficacy Study to Determine Anti-Asthmatic Effect of Esomeprazole Magnesium; Nexium Reflux Asthma

ClinicalTrials.gov ID: NCT00317044

Public ClinicalTrials.gov record NCT00317044. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 10:49 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 6-month Randomized, Double-blind, Parallel-group, Multicentre, Placebo-controlled Phase II Study to Compare Anti-asthmatic Effect and Safety of Esomeprazole (Nexium®) 40 mg Twice Daily or 40 mg Once Daily With Placebo in Adults With Asthma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether treatment with esomeprazole for 6 months will improve asthma in adult patients with moderate to severe asthma and symptoms of gastroesophageal reflux disease.

Study identification

NCT ID
NCT00317044
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
961 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2006 (Type not available)
Primary completion
Jul 2008 (Actual)
Completion
Jul 2008 (Actual)
Last update posted
Jun 9, 2014

2006 – 2008

United States locations

U.S. sites
27
U.S. states
20
U.S. cities
27
Facility City State ZIP Site status
Research Site Birmingham Alabama — —
Research Site Scottsdale Arizona — —
Research Site Little Rock Arkansas — —
Research Site Fountain Valley California — —
Research Site Miami Florida — —
Research Site Atlanta Georgia — —
Research Site Stockbridge Georgia — —
Research Site Normal Illinois — —
Research Site Overland Park Kansas — —
Research Site Wichita Kansas — —
Research Site Mandeville Louisiana — —
Research Site Wheaton Maryland — —
Research Site St Louis Missouri — —
Research Site Papillion Nebraska — —
Research Site Asheville North Carolina — —
Research Site Cincinnati Ohio — —
Research Site Sylvania Ohio — —
Research Site Medford Oregon — —
Research Site Pittsburgh Pennsylvania — —
Research Site Upland Pennsylvania — —
Research Site Charleston South Carolina — —
Research Site Austin Texas — —
Research Site Houston Texas — —
Research Site San Antonio Texas — —
Research Site Kirkland Washington — —
Research Site Seattle Washington — —
Research Site Greenfield Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 103 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00317044, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 9, 2014 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00317044 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →