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Last Updated: November 16, 2024

CLINICAL TRIALS PROFILE FOR DEXILANT


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All Clinical Trials for dexilant

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00251693 ↗ Efficacy and Safety of Dexlansoprazole MR and Lansoprazole on Healing of Erosive Esophagitis Completed Takeda Phase 3 2005-12-01 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.
NCT00251719 ↗ Efficacy and Safety of Dexlansoprazole MR and Lansoprazole on Healing of Erosive Esophagitis Completed Takeda Phase 3 2005-12-01 This is a study to assess the efficacy and safety of 8 weeks of treatment with Dexlansoprazole modified release (MR)(60 mg daily and 90 mg daily) compared to Lansoprazole (30 mg daily) in healing subjects with endoscopically proven erosive esophagitis.
NCT00251745 ↗ Efficacy and Safety of Dexlansoprazole Modified Release Formulation to Treat Heartburn Completed Takeda Phase 3 2005-12-01 The purpose of this study is to assess the efficacy and safety of daily treatment with Dexlansoprazole modified release (MR) (60 mg or 90 mg once daily [QD]) compared to placebo QD in relief of daytime and nighttime heartburn over 4 weeks in subjects with gastroesophageal reflux disease (GERD).
NCT00251758 ↗ Safety and Efficacy of Dexlansoprazole Modified Release Formulation to Treat Heartburn Completed Takeda Phase 3 2005-12-01 The purpose of this study is to assess the efficacy and safety of daily treatment with Dexlansoprazole modified release (MR) (60 mg or 90 mg once daily [QD]) compared to placebo QD in relief of daytime and nighttime heartburn over 4 weeks in subjects with gastroesophageal reflux disease (GERD).
NCT00255151 ↗ Comparison of Dexlansoprazole MR to Placebo on the Ability to Maintain Healing in Subjects With Healed Erosive Esophagitis Completed Takeda Phase 3 2006-01-01 The purpose of this study is to assess the ability of once-daily (QD) treatment with Dexlansoprazole modified-release (MR) 60 mg and 90 mg and placebo in maintaining healing of erosive esophagitis (EE).
NCT00255164 ↗ Efficacy and Safety of Dexlansoprazole MR on Maintaining Healing in Subjects With Healed Erosive Esophagitis Completed Takeda Phase 3 2006-01-01 The purpose of this study is to assess the ability of once-daily (QD) treatment with Dexlansoprazole modified-release (MR) 60 mg and 90 mg and placebo in maintaining healing of erosive esophagitis (EE).
NCT00255190 ↗ Safety and Quality of Life Study of Dexlansoprazole Modified Release Formulation to Treat Heartburn Completed Takeda Phase 3 2006-01-01 The purpose of this study is to determine the long-term safety profile of daily treatment with dexlansoprazole MR in subjects with gastroesophageal reflux disease.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for dexilant

Condition Name

Condition Name for dexilant
Intervention Trials
Gastroesophageal Reflux Disease 7
Esophagitis, Peptic 5
Esophagitis, Reflux 5
Gastroesophageal Reflux 5
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Condition MeSH

Condition MeSH for dexilant
Intervention Trials
Gastroesophageal Reflux 17
Esophagitis, Peptic 15
Esophagitis 10
Laryngopharyngeal Reflux 2
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Clinical Trial Locations for dexilant

Trials by Country

Trials by Country for dexilant
Location Trials
United States 450
Mexico 14
Canada 12
India 9
Germany 8
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Trials by US State

Trials by US State for dexilant
Location Trials
California 18
Illinois 17
Arizona 16
Texas 16
Ohio 16
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Clinical Trial Progress for dexilant

Clinical Trial Phase

Clinical Trial Phase for dexilant
Clinical Trial Phase Trials
Phase 4 4
Phase 3 11
Phase 2 5
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Clinical Trial Status

Clinical Trial Status for dexilant
Clinical Trial Phase Trials
Completed 21
Terminated 2
Unknown status 2
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Clinical Trial Sponsors for dexilant

Sponsor Name

Sponsor Name for dexilant
Sponsor Trials
Takeda 22
Vanderbilt University 2
Mayo Clinic 2
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Sponsor Type

Sponsor Type for dexilant
Sponsor Trials
Industry 23
Other 15
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