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Anabolic bone therapies in 2014

New bone-forming treatments for osteoporosis

In 2014, two phase II clinical studies reported rapid, impressive increases in BMD in women with low bone mass who were treated with sclerostin inhibitors for 1 year. The antifracture efficacy and tolerability of these new, bone-building therapies are currently being investigated in phase III clinical trials.

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Figure 1: Bone turnover in response to anabolic bone therapies.

References

  1. Tsai, J. N. et al. Teriparatide and denosumab, alone or combined in women with postmenopausal osteoporosis: the DATA study randomized trial. Lancet 382, 50–56 (2013).

    Article  CAS  Google Scholar 

  2. Leder, B. Z. et al. Two years of denosumab and teriparatide administration in postmenopausal women with osteoporosis (the DATA extension study): a randomized controlled trial. J. Clin. Endocrinol. Metab. 99, 1694–1700 (2014).

    Article  CAS  Google Scholar 

  3. Ke, H. Z., Richards, W. G., Li, X. & Ominsky, M. S. Sclerostin and Dickkopf-1 as therapeutic targets in bone diseases. Endocr. Rev. 33, 747–783 (2012).

    Article  CAS  Google Scholar 

  4. Moester, M. J., Papapoulos, S. E., Lowik, C. W. & van Bezooijen, R. L. Slerostin: current knowledge and future perspectives. Calcif. Tissue Int. 87, 99–107 (2010).

    Article  CAS  Google Scholar 

  5. Li, X. et al. Sclerostin antibody treatment increases bone formation, bone mass and bone strength in a rat model of postmenopausal osteoporosis. J. Bone Miner. Res. 24, 578–588 (2009).

    Article  CAS  Google Scholar 

  6. Ominsky, M. S. et al. Two doses of sclerostin antibody in cynomologous monkeys increase bone formation, bone mineral density and bone stength. J. Bone Miner. Res. 25, 948–959 (2010).

    Article  CAS  Google Scholar 

  7. Padhi, D., Jang, G., Struch, B., Fang, L. & Posrar, E. Single-dose, placebo-controlled, randomized study of AMG 785, a sclerostin monoclonal antibody. J. Bone Miner. Res. 26, 19–26 (2011).

    Article  CAS  Google Scholar 

  8. Recker, R. et al. A randomized, double-blind phase 2 clinical trial of blosozumab, a sclerostin antibody, in postmenopausal women with low bone mineral density. J. Bone Miner. Res. http://dx.doi.org/10.1002/jbmr.2351.

  9. McClung, M. R. et al. Romosozumab in postmenopausal women with low bone mineral density. N. Engl. J. Med. 370, 412–420 (2014).

    Article  CAS  Google Scholar 

  10. Ominsky, M. S., Niu, Q.-T., Li, C., Li, X. & Ke, H. Z. Tissue-level mechanisms responsible for the increase in bone formation and bone volume by sclerostin antibody. J. Bone Miner. Res. 29, 1424–1430 (2014).

    Article  CAS  Google Scholar 

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Acknowledgements

The author's studies on sclerostin are supported by and carried out within the FP7 programme TALOS, which is funded by the European Commission (Grant Number: TALOS:Health-F2-2008-201,099).

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Correspondence to Socrates E. Papapoulos.

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The author has received consulting fees and speaker honoraria from Amgen and UCB.

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Papapoulos, S. New bone-forming treatments for osteoporosis. Nat Rev Endocrinol 11, 69–70 (2015). https://doi.org/10.1038/nrendo.2014.214

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