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Clinical Trial Summary

The purpose of this study is to evaluate the effect of dexlansoprazole modified release (MR), once daily (QD), on bone homeostasis.


Clinical Trial Description

Research on drugs that affect bone homeostasis have shown changes in levels of bone formation and resorption biomarkers. This study will evaluate the effect of dexlansoprazole on bone homeostasis by assessing changes in biochemical markers of bone formation and bone resorption. This study will also assess changes in bone mineral density by dual-energy x-ray absorptiometry scan and other markers of bone homeostasis. The study will consist of a 12-week screening period, a 26-week treatment period with a total of 5 visits during the treatment period and a follow-up visit at Week 52 for bone mineral density assessment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01216293
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 1
Start date November 1, 2010
Completion date February 1, 2015

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