A Randomized Study to Evaluate Safety and Efficacy of Transitioning Therapy From Alendronate to Denosumab (AMG 162) in Postmenopausal Women with Low Bone Mineral Density

Mise à jour : Il y a 4 ans
Référence : EUCTR2006-000849-19

Femme Homme

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Extrait

The primary objective is to evaluate the effect of denosumab 60 mg q 6 months on total hip bone mineral density (BMD) at 12 months in postmenopausal women with low BMD previously treated with alendronate 70 mg QW or equivalent compared to that in subjects continuing on alendronate therapy.


Critère d'inclusion

  • Postmenopausal osteoporosis /osteopenia