Clinical trial
Efficacy and Safety of Dexlansoprazole Modified Release Formulation to Treat…
NCT00251745 · Takeda, Industry · Completed
Key facts
| NCT number | NCT00251745 |
|---|---|
| Title | Efficacy and Safety of Dexlansoprazole Modified Release Formulation to Treat Heartburn |
| Official title | A Phase 3 Study to Evaluate the Efficacy and Safety of Dexlansoprazole MR (60 mg Once-Daily (QD) and 90 mg QD) Compared to Placebo on Symptom Relief in Subjects With Symptomatic Non-Erosive Gastroesophageal Reflux Disease (GERD) |
| Lead sponsor | Takeda, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Gastroesophageal Reflux Disease |
| Intervention type | Drug |
| Interventions | Dexlansoprazole MR, Placebo |
| Enrollment | 908 |
| Start date | Dec 1, 2005 |
| Primary completion | May 1, 2006 |
| Completion | May 1, 2006 |
| First posted | Nov 10, 2005 |
| Last update posted | Apr 28, 2011 |
| Countries | United States |
At a glance
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: