A Phase IIa, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of Odanacatib (MK-0822) on Bone Mineral Density (BMD) and Overall Safety in the Treatment of Osteoporosis in Postmenopausal Women Previously Treated with Alendronate

Estudio en fase IIa aleatorizado, doble ciego, controlado con placebo para evaluar los efectos de odanacatib (MK-0822) sobre la densidad mineral ósea (DMO) y la seguridad general en el tratamiento de la osteoporosis en mujeres posmenopáusicas previamente tratadas con alendronato A Phase IIa, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effects of Odanacatib (MK-0822) on Bone Mineral Density (BMD) and Overall Safety in the Treatment of Osteoporosis in Postmenopausal Women Previously Treated with Alendronate

Registry ID
EUCTR2008-008257-30
Source registry
EUCTR
Status
Completed
Phase
PHASE2
Sponsor
Merck & Co. Inc
Start date
2009-04-10
Completion date
2011-09-15
Last update
2026-08-16

Conditions

Summary

To evaluate the effect of treatment on BMD percent change from baseline at the femoral neck site assessed by DXA compared to placebo at the end of 24 months.

Locations

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