This study will evaluate the therapeutic effects and safety of odanacatib on bone mineral density in osteoporotic postmenopausal women who were previously treated with alendronate.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Odanacatib 50 mg compressed tablet will be administered orally, once-a-week, for 24 months
Alendronate 70 mg compressed tablets will be administered orally, once-a-week, for 24 months; and a reduced dose of 35 mg will be administered in the same fashion to a subset of women, Japanese participants only, for the same 24-month duration.
One compressed tablet administered orally, once-a-week, for 24 months.
Percent Change from Baseline in Bone Mineral Density (BMD) of the Femoral Neck
Time frame: Baseline and Month 24
Percent Change from Baseline in BMD of the Lumbar Spine, Total Hip, and Trochanter
Time frame: Baseline and Month 24
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Two (2) 2800 IU compressed tablets administered orally, once-a-week, for 24 months.
Dietary and supplemental sources, taken as needed, to ensure a total daily calcium intake of approximately 1200 mg.
One compressed tablet administered orally, once-a-week, for 24 months.