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Taylor and Francis Group, Expert Opinion on Drug Metabolism and Toxicology, 7(9), p. 883-892, 2013

DOI: 10.1517/17425255.2013.794221

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Pharmacokinetic evaluation of bazedoxifene for the treatment of osteoporosis

Journal article published in 2013 by Davide Gatti, Maurizio Rossini ORCID, Ignazio Sblendorio, Stefano Lello
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

INTRODUCTION: Bazedoxifene is a third-generation Selective Estrogen Receptor Modulator, developed on raloxifene's model, and investigated as treatment for postmenopausal osteoporosis and menopause management. Clinical trial have shown that bazedoxifene is effective as raloxifene in preventing bone loss in women at risk of osteoporosis and that in patients with osteoporosis it is effective in reducing the incidence of new vertebral fracture with a protection maintained for up 7 years. AREAS COVERED: This drug evaluation presents the antifracture efficacy of bazedoxifine and evidence that it, unlike raloxifene, can reduce the rate of non-vertebral fractures in high-risk patients. The authors also review the effects of bazedoxifine has on reproduction tissues as well as the on lipid pattern. Additionally, the authors present the safety profile of bazedoxifine and discuss its prospects, specifically in relation to conjugated estrogen. EXPERT OPINION: Despite its peculiar profile, bazedoxifene could be considered as a second-line therapy for women