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Completed Phase 3 Interventional Results available

Efficacy and Safety of Dexlansoprazole MR and Lansoprazole on Healing of Erosive Esophagitis

ClinicalTrials.gov ID: NCT00251693

Public ClinicalTrials.gov record NCT00251693. 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, 6:35 AM 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 Phase 3 Study to Evaluate the Efficacy and Safety of TAK-390MR (60 mg Once- Daily [QD] and 90 mg QD) and an Active Comparator, Lansoprazole (30 mg QD) on Healing of Erosive Esophagitis

Brief summary

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

The purpose of this study is to assess the efficacy and safety of 8 weeks of once-daily (QD) treatment with dexlansoprazole modified release (MR) 60 mg or 90 mg or lansoprazole 30 mg in healing subjects with endoscopically proven erosive esophagitis.

Study identification

NCT ID
NCT00251693
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
2,038 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Dec 2005 (Type not available)
Primary completion
Jan 2007 (Actual)
Completion
Jan 2007 (Actual)
Last update posted
Feb 3, 2012

2005 – 2007

United States locations

U.S. sites
96
U.S. states
31
U.S. cities
96
Facility City State ZIP Site status
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Not listed Charlotte North Carolina — —
Not listed Elkin North Carolina — —
Not listed Greensboro North Carolina — —
Not listed Hickory North Carolina — —
Not listed Salisbury North Carolina — —
Not listed Statesville North Carolina — —
Not listed Winston-Salem North Carolina — —
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Not listed Portland Oregon — —
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Not listed Hermitage Tennessee — —
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Not listed Beaumont Texas — —
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Not listed Bountiful Utah — —
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Not listed Salt Lake City Utah — —
Not listed West Jordan Utah — —
Not listed Chesapeake Virginia — —
Not listed Danville Virginia — —
Not listed Spokane Washington — —
Not listed Milwaukee Wisconsin — —
Not listed Monroe 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 44 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00251693, 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 Feb 3, 2012 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00251693 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →