Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2791498 | Best Practice & Research Clinical Endocrinology & Metabolism | 2014 | 15 Pages |
Abstract
Despite the availability of efficacious treatments for fracture reduction in patients with osteoporosis, there are still unmet needs requiring a broader range of therapeutics. In particular, agents that are capable of replacing already lost bone and that also drastically reduce the risk of non-vertebral fractures are needed. Studies of rare bone diseases in humans and animal genetics have identified targets in bone cells for the development of therapies for osteoporosis with novel mechanisms of action. Here, we review these new developments, with emphasis on inhibitors of cathepsin K in osteoclasts and sclerostin in osteocytes, which are currently studied in phase 3 clinical trials.
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Authors
Natasha M. Appelman-Dijkstra, Socrates E. Papapoulos,