Skip to main content
Top
Published in: Drugs & Aging 5/2007

01-05-2007 | Leading Article

Selective Estrogen Receptor Modulators for Postmenopausal Osteoporosis

Current State of Development

Authors: Dr Luigi Gennari, Daniela Merlotti, Fabrizio Valleggi, Giuseppe Martini, Ranuccio Nuti

Published in: Drugs & Aging | Issue 5/2007

Login to get access

Abstract

Selective estrogen receptor modulators (SERMs) are structurally different compounds that interact with intracellular estrogen receptors in target organs as estrogen receptor agonists and antagonists. These drugs have been intensively studied over the past decade and have proven to be a highly versatile group for the treatment of different conditions associated with aging, including hormone-responsive cancer and osteoporosis. Tamoxifen and toremifene are currently used to treat advanced breast cancer and also have beneficial effects on bone mineral density and serum lipids in postmenopausal women. Raloxifene is the only SERM approved worldwide for the prevention and treatment of postmenopausal osteoporosis and vertebral fractures. However, although these SERMs have many benefits, they may also be responsible for some potentially very serious adverse effects, such as thromboembolic disorders and, in the case of tamoxifen, uterine cancer. These adverse effects represent a major concern given that long-term therapy is required to prevent osteoporosis. Moreover, both preclinical and clinical reports suggest that tamoxifen, toremifene and raloxifene are considerably less potent than estrogen.
The search for the ‘ideal’ SERM, which would have estrogenic effects on bone and serum lipids, neutral effects on the uterus, and antiestrogenic effects on breast tissue, but none of the adverse effects associated with current therapies, is currently under way. Ospemifene, lasofoxifene, bazedoxifene and arzoxifene, which are new SERM molecules with potential greater efficacy and potency than previous SERMs, are currently under investigation for use in the treatment and prevention of osteoporosis. These drugs have been shown to be comparably effective to conventional hormone replacement therapy in animal models of osteoporosis, with potential indications for an improved safety profile. Clinical efficacy data from ongoing phase III trials are awaited so that a true understanding of the therapeutic potential of these compounds can be obtained.
Footnotes
1
The use of trade names is for product identification purposes only and does not imply endorsement.
 
Literature
1.
go back to reference Osteoporosis prevention, diagnosis, and therapy consensus statement 2000. JAMA 2001; 285: 785–95 Osteoporosis prevention, diagnosis, and therapy consensus statement 2000. JAMA 2001; 285: 785–95
2.
go back to reference Melton III LJ, Chrischilles EA, Cooper C, et al. Perspective: how many women have osteoporosis? J Bone Miner Res 1992; 7: 1005–10PubMedCrossRef Melton III LJ, Chrischilles EA, Cooper C, et al. Perspective: how many women have osteoporosis? J Bone Miner Res 1992; 7: 1005–10PubMedCrossRef
3.
go back to reference Barrett-Connor E. The economic and human costs of osteoporotic fracture. Am J Med 1995; 98: 3S–8SPubMedCrossRef Barrett-Connor E. The economic and human costs of osteoporotic fracture. Am J Med 1995; 98: 3S–8SPubMedCrossRef
4.
go back to reference Melton LJ, Atkinson EJ, Cooper C, et al. Vertebral fractures predict subsequent fracture. Osteoporos Int 1999; 10: 214–21PubMedCrossRef Melton LJ, Atkinson EJ, Cooper C, et al. Vertebral fractures predict subsequent fracture. Osteoporos Int 1999; 10: 214–21PubMedCrossRef
5.
go back to reference Minne H. IOF International Survey 1999. Nyon: International Osteoporosis Foundation (IOF), 1999 Nov Minne H. IOF International Survey 1999. Nyon: International Osteoporosis Foundation (IOF), 1999 Nov
6.
go back to reference Cummings SR, Black DM, Nevitt MC, et al. Bone density at various sites for prediction of hip fractures. Lancet 1993; 341: 72–5PubMedCrossRef Cummings SR, Black DM, Nevitt MC, et al. Bone density at various sites for prediction of hip fractures. Lancet 1993; 341: 72–5PubMedCrossRef
7.
go back to reference Hui SL, Slemenda CW, Carey MA, et al. Choosing between predictors of fractures. J Bone Miner Res 1995; 10: 1816–22PubMedCrossRef Hui SL, Slemenda CW, Carey MA, et al. Choosing between predictors of fractures. J Bone Miner Res 1995; 10: 1816–22PubMedCrossRef
8.
go back to reference Cummings SR, Black DM, Nevitt MC, et al. Appendicular bone density and age predict hip fracture in women: the study of Osteoporotic Fractures Research Group. JAMA 1990; 263: 665–8PubMedCrossRef Cummings SR, Black DM, Nevitt MC, et al. Appendicular bone density and age predict hip fracture in women: the study of Osteoporotic Fractures Research Group. JAMA 1990; 263: 665–8PubMedCrossRef
9.
go back to reference Black DM, Cummings SR, Genant HK, et al. Axial and appendicular bone density predict fractures in older women. J Bone Miner Res 1992; 7: 633–8PubMedCrossRef Black DM, Cummings SR, Genant HK, et al. Axial and appendicular bone density predict fractures in older women. J Bone Miner Res 1992; 7: 633–8PubMedCrossRef
10.
go back to reference Riggs BL, Khosla S, Melton III LJ. A unitary model of involu-tional osteoporosis: estrogen deficiency causes both type I and type II osteoporosis in postmenopausal women and contributes to bone loss in aging men. J Bone Miner Res 1998; 13: 763–73PubMedCrossRef Riggs BL, Khosla S, Melton III LJ. A unitary model of involu-tional osteoporosis: estrogen deficiency causes both type I and type II osteoporosis in postmenopausal women and contributes to bone loss in aging men. J Bone Miner Res 1998; 13: 763–73PubMedCrossRef
11.
go back to reference Khosla S, Melton III LJ, Riggs BL. Clinical review 144: estrogen and the male skeleton. J Clin Endocrinol Metab 2002; 87: 1443–50PubMedCrossRef Khosla S, Melton III LJ, Riggs BL. Clinical review 144: estrogen and the male skeleton. J Clin Endocrinol Metab 2002; 87: 1443–50PubMedCrossRef
12.
go back to reference Gennari L, Nuti R, Bilezikian JP. Aromatase activity and bone homeostasis in men. J Clin Endocrinol Metab 2004; 89: 5898–907PubMedCrossRef Gennari L, Nuti R, Bilezikian JP. Aromatase activity and bone homeostasis in men. J Clin Endocrinol Metab 2004; 89: 5898–907PubMedCrossRef
13.
go back to reference Riggs BL, Khosla S, Melton III LJ. Sex steroids and the construction and conservation of the adult skeleton. Endo Rev 2002; 23: 279–302CrossRef Riggs BL, Khosla S, Melton III LJ. Sex steroids and the construction and conservation of the adult skeleton. Endo Rev 2002; 23: 279–302CrossRef
14.
go back to reference Green S, Walter P, Kumar V, et al. Human estrogen receptor cDNA: sequence, expression and homology to v-erb-A. Nature 1986; 320: 134–9PubMedCrossRef Green S, Walter P, Kumar V, et al. Human estrogen receptor cDNA: sequence, expression and homology to v-erb-A. Nature 1986; 320: 134–9PubMedCrossRef
15.
go back to reference Greene GL, Gilna P, Waterfield M, et al. Sequence and expression of human estrogen receptor complementary DNA. Science 1986; 231: 1150–4PubMedCrossRef Greene GL, Gilna P, Waterfield M, et al. Sequence and expression of human estrogen receptor complementary DNA. Science 1986; 231: 1150–4PubMedCrossRef
16.
go back to reference Kuiper GGJM, Enmark E, Pelto-Huikko M, et al. Cloning of a novel estrogen receptor expressed in rat prostate and ovary. Proc Natl Acad Sci U S A 1996; 93: 5925–30PubMedCrossRef Kuiper GGJM, Enmark E, Pelto-Huikko M, et al. Cloning of a novel estrogen receptor expressed in rat prostate and ovary. Proc Natl Acad Sci U S A 1996; 93: 5925–30PubMedCrossRef
17.
go back to reference Mosselman S, Polman J, Dijkema R. ER beta: identification and characterization of a novel human estrogen receptor. FEBS Lett 1996; 392: 49–53PubMedCrossRef Mosselman S, Polman J, Dijkema R. ER beta: identification and characterization of a novel human estrogen receptor. FEBS Lett 1996; 392: 49–53PubMedCrossRef
18.
go back to reference Gustafsson JA. Estrogen receptor beta: a new dimension in estrogen mechanism of action. J Endocrinol 1999 Dec; 163(3): 379–83PubMedCrossRef Gustafsson JA. Estrogen receptor beta: a new dimension in estrogen mechanism of action. J Endocrinol 1999 Dec; 163(3): 379–83PubMedCrossRef
19.
go back to reference Bord S, Horner A, Beavan S, et al. Estrogen receptors alpha and beta are differentially expressed in developing human bone. J Clin Endocrinol Metab 2001 May; 86(5): 2309–14PubMedCrossRef Bord S, Horner A, Beavan S, et al. Estrogen receptors alpha and beta are differentially expressed in developing human bone. J Clin Endocrinol Metab 2001 May; 86(5): 2309–14PubMedCrossRef
20.
go back to reference Writing Group for the Women’s Health Initiative Investigators. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women’s Health Initiative randomized controlled trial. JAMA 2002; 288: 321–33CrossRef Writing Group for the Women’s Health Initiative Investigators. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women’s Health Initiative randomized controlled trial. JAMA 2002; 288: 321–33CrossRef
21.
go back to reference Chlebowski RT, Wactawski-Wende J, Ritenbaugh C, et al. Women’s Health Initiative Investigators. Estrogen plus progestin and colorectal cancer in postmenopausal women. N Engl J Med 2004; 350: 991–1004PubMedCrossRef Chlebowski RT, Wactawski-Wende J, Ritenbaugh C, et al. Women’s Health Initiative Investigators. Estrogen plus progestin and colorectal cancer in postmenopausal women. N Engl J Med 2004; 350: 991–1004PubMedCrossRef
22.
go back to reference Manson JE, Hsia J, Johnson KC, et al. Women’s Health Initiative Investigators. Estrogen plus progestin and the risk of coronary heart disease. N Engl J Med 2003; 349: 523–34PubMedCrossRef Manson JE, Hsia J, Johnson KC, et al. Women’s Health Initiative Investigators. Estrogen plus progestin and the risk of coronary heart disease. N Engl J Med 2003; 349: 523–34PubMedCrossRef
23.
go back to reference The Writing Group for the PEPI Trial. Effects of estrogen or estrogen/progestin regimens on heart disease risk factors in postmenopausal women: the Postmenopausal Estrogen/Progestin Interventions (PEPI) Trial [published erratum appears in JAMA 1995; 274: 1676]. JAMA 1995; 273: 199–208CrossRef The Writing Group for the PEPI Trial. Effects of estrogen or estrogen/progestin regimens on heart disease risk factors in postmenopausal women: the Postmenopausal Estrogen/Progestin Interventions (PEPI) Trial [published erratum appears in JAMA 1995; 274: 1676]. JAMA 1995; 273: 199–208CrossRef
24.
go back to reference Vassilopoulou-Sellin R. Breast cancer and hormonal replacement therapy. Ann N Y Acad Sci 2003; 997: 341–50PubMedCrossRef Vassilopoulou-Sellin R. Breast cancer and hormonal replacement therapy. Ann N Y Acad Sci 2003; 997: 341–50PubMedCrossRef
25.
go back to reference HRT: what are women (and their doctors) to do? [editorial]. Lancet 2004; 364: 2069–70 HRT: what are women (and their doctors) to do? [editorial]. Lancet 2004; 364: 2069–70
26.
27.
go back to reference Cho CH, Nuttall ME. Therapeutic potential of oestrogen receptor ligands in development for osteoporosis. Expert Opin Emerg Drugs 2001; 6: 137–54PubMedCrossRef Cho CH, Nuttall ME. Therapeutic potential of oestrogen receptor ligands in development for osteoporosis. Expert Opin Emerg Drugs 2001; 6: 137–54PubMedCrossRef
28.
go back to reference Riggs L, Hartmann LC. Selective estrogen-receptor modulators-mechanisms of action and application to clinical practice. N Engl J Med 2003; 348: 618–29PubMedCrossRef Riggs L, Hartmann LC. Selective estrogen-receptor modulators-mechanisms of action and application to clinical practice. N Engl J Med 2003; 348: 618–29PubMedCrossRef
29.
go back to reference Shiau AK, Barstad D, Loria PM, et al. The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen. Cell 1998; 95: 927–37PubMedCrossRef Shiau AK, Barstad D, Loria PM, et al. The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen. Cell 1998; 95: 927–37PubMedCrossRef
30.
go back to reference Brzozowski AM, Pike AC, Dauter Z, et al. Molecular basis of agonism and antagonism in the oestrogen receptor. Nature 1997; 389: 753–8PubMedCrossRef Brzozowski AM, Pike AC, Dauter Z, et al. Molecular basis of agonism and antagonism in the oestrogen receptor. Nature 1997; 389: 753–8PubMedCrossRef
31.
go back to reference Paige LA, Christensen DJ, Grøn H, et al. Estrogen receptor (ER)modulators each induce distinct conformational changes in ERa and ERb. Proc Natl Acad Sci U S A 1999; 96: 3999–4004PubMedCrossRef Paige LA, Christensen DJ, Grøn H, et al. Estrogen receptor (ER)modulators each induce distinct conformational changes in ERa and ERb. Proc Natl Acad Sci U S A 1999; 96: 3999–4004PubMedCrossRef
32.
go back to reference Morello KC, Wurz GT, DeGregorio MW. SERMs: current status and future trends. Crit Rev Oncol Hematol 2002; 43: 63–76PubMedCrossRef Morello KC, Wurz GT, DeGregorio MW. SERMs: current status and future trends. Crit Rev Oncol Hematol 2002; 43: 63–76PubMedCrossRef
33.
go back to reference Delmas PD, Bjarnason NH, Mitlak BH, et al. Effects of ralox-ifene on bone mineral density, serum cholesterol concentrations, and uterine endometrium in postmenopausal women. N Engl J Med 1997; 337: 1641–7PubMedCrossRef Delmas PD, Bjarnason NH, Mitlak BH, et al. Effects of ralox-ifene on bone mineral density, serum cholesterol concentrations, and uterine endometrium in postmenopausal women. N Engl J Med 1997; 337: 1641–7PubMedCrossRef
34.
go back to reference Lufkin EG, Whitaker MD, Nickelsen T, et al. Treatment of established postmenopausal osteoporosis with raloxifene: a randomized trial. J Bone Miner Res 1998; 13: 1747–54PubMedCrossRef Lufkin EG, Whitaker MD, Nickelsen T, et al. Treatment of established postmenopausal osteoporosis with raloxifene: a randomized trial. J Bone Miner Res 1998; 13: 1747–54PubMedCrossRef
35.
go back to reference Ettinger B, Black DM, Mitlak BH, et al. Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: results from a 3-year randomized clinical trial. Multiple Outcomes of Raloxifene Evaluation (MORE) Investigators [published erratum appears in JAMA 1999 Dec 8; 282(22): 2124]. JAMA 1999 Aug 18; 282(7): 637–45PubMedCrossRef Ettinger B, Black DM, Mitlak BH, et al. Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: results from a 3-year randomized clinical trial. Multiple Outcomes of Raloxifene Evaluation (MORE) Investigators [published erratum appears in JAMA 1999 Dec 8; 282(22): 2124]. JAMA 1999 Aug 18; 282(7): 637–45PubMedCrossRef
36.
go back to reference Siris ES, Harris ST, Eastell R, et al. Continuing Outcomes Relevant to Evista (CORE) Investigators. Skeletal effects of raloxifene after 8 years: results from the continuing outcomes relevant to Evista (CORE) study. J Bone Miner Res 2005 Sep; 20(9): 1514–24PubMedCrossRef Siris ES, Harris ST, Eastell R, et al. Continuing Outcomes Relevant to Evista (CORE) Investigators. Skeletal effects of raloxifene after 8 years: results from the continuing outcomes relevant to Evista (CORE) study. J Bone Miner Res 2005 Sep; 20(9): 1514–24PubMedCrossRef
37.
go back to reference Vogel VG, Costantino JP, Wickerham DL, et al. National Surgical Adjuvant Breast and Bowel Project (NSABP). Effects of tamoxifen vs raloxifene on the risk of developing invasive breast cancer and other disease outcomes: the NSABP Study of Tamoxifen and Raloxifene (STAR) P-2 trial. JAMA 2006 Jun 21; 295(23): 2727–41PubMedCrossRef Vogel VG, Costantino JP, Wickerham DL, et al. National Surgical Adjuvant Breast and Bowel Project (NSABP). Effects of tamoxifen vs raloxifene on the risk of developing invasive breast cancer and other disease outcomes: the NSABP Study of Tamoxifen and Raloxifene (STAR) P-2 trial. JAMA 2006 Jun 21; 295(23): 2727–41PubMedCrossRef
38.
go back to reference Stefanick ML. Risk-benefit profiles of raloxifene for women. N Engl J Med 2006 Jul 13; 355(2): 190–2PubMedCrossRef Stefanick ML. Risk-benefit profiles of raloxifene for women. N Engl J Med 2006 Jul 13; 355(2): 190–2PubMedCrossRef
39.
go back to reference Barrett-Connor E, Mosca L, Collins P, et al. Raloxifene Use for The Heart (RUTH) Trial Investigators. Effects of raloxifene on cardiovascular events and breast cancer in postmenopausal women. N Engl J Med 2006 Jul 13; 355(2): 125–37PubMedCrossRef Barrett-Connor E, Mosca L, Collins P, et al. Raloxifene Use for The Heart (RUTH) Trial Investigators. Effects of raloxifene on cardiovascular events and breast cancer in postmenopausal women. N Engl J Med 2006 Jul 13; 355(2): 125–37PubMedCrossRef
40.
go back to reference Jordan VC, Phelps E, Lindgren JU. Effects of anti-estrogens on bone in castrated and intact female rats. Breast Cancer Res Treat 1987; 10: 31–5PubMedCrossRef Jordan VC, Phelps E, Lindgren JU. Effects of anti-estrogens on bone in castrated and intact female rats. Breast Cancer Res Treat 1987; 10: 31–5PubMedCrossRef
41.
go back to reference Turner RT, Wakley GK, Hannon KS, et al. Tamoxifen inhibits osteoclast-mediated resorption of trabecular bone in ovarian hormone-deficient rats. Endocrinology 1988; 122: 1146–50PubMedCrossRef Turner RT, Wakley GK, Hannon KS, et al. Tamoxifen inhibits osteoclast-mediated resorption of trabecular bone in ovarian hormone-deficient rats. Endocrinology 1988; 122: 1146–50PubMedCrossRef
42.
go back to reference Turken S, Siris E, Seldin D, et al. Effects of tamoxifen on spinal bone density in women with breast cancer. J Natl Cancer Inst 1989; 81: 1086–8PubMedCrossRef Turken S, Siris E, Seldin D, et al. Effects of tamoxifen on spinal bone density in women with breast cancer. J Natl Cancer Inst 1989; 81: 1086–8PubMedCrossRef
43.
go back to reference Love RR, Mazess RB, Barden HS, et al. Effects of tamoxifen on bone mineral density in postmenopausal women with breast cancer. N Engl J Med 1992; 326: 852–6PubMedCrossRef Love RR, Mazess RB, Barden HS, et al. Effects of tamoxifen on bone mineral density in postmenopausal women with breast cancer. N Engl J Med 1992; 326: 852–6PubMedCrossRef
44.
go back to reference Love RR, Barden HS, Mazess RB, et al. Effect of tamoxifen on lumbar spine bone mineral density in postmenopausal women after 5 years. Arch Intern Med 1994; 154: 2585–8PubMedCrossRef Love RR, Barden HS, Mazess RB, et al. Effect of tamoxifen on lumbar spine bone mineral density in postmenopausal women after 5 years. Arch Intern Med 1994; 154: 2585–8PubMedCrossRef
45.
go back to reference Fisher B, Costantino JP, Wickerham DL, et al. Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study. J Natl Cancer Inst 1998 Sep 16; 90(18): 1371–88PubMedCrossRef Fisher B, Costantino JP, Wickerham DL, et al. Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study. J Natl Cancer Inst 1998 Sep 16; 90(18): 1371–88PubMedCrossRef
46.
go back to reference Fisher B, Costantino JP, Wickerham DL, et al. Tamoxifen for the prevention of breast cancer: current status of the National Surgical Adjuvant Breast and Bowel Project P-l study. J Natl Cancer Inst 2005 Nov 6; 97(22): 1652–62PubMedCrossRef Fisher B, Costantino JP, Wickerham DL, et al. Tamoxifen for the prevention of breast cancer: current status of the National Surgical Adjuvant Breast and Bowel Project P-l study. J Natl Cancer Inst 2005 Nov 6; 97(22): 1652–62PubMedCrossRef
47.
go back to reference Kristensen B, Ejlertsen B, Mouridsen HT, et al. Femoral fractures in postmenopausal breast cancer patients treated with adjuvant tamoxifen. Breast Cancer Res Treat 1996; 39(3): 321–6PubMedCrossRef Kristensen B, Ejlertsen B, Mouridsen HT, et al. Femoral fractures in postmenopausal breast cancer patients treated with adjuvant tamoxifen. Breast Cancer Res Treat 1996; 39(3): 321–6PubMedCrossRef
48.
go back to reference Marttunen MB, Hietanen P, Tiitinen A, et al. Comparison of effects of tamoxifen and toremifene on bone biochemistry and bone mineral density in postmenopausal breast cancer patients. J Clin Endocrinol Metab 1998; 83: 1158–62PubMedCrossRef Marttunen MB, Hietanen P, Tiitinen A, et al. Comparison of effects of tamoxifen and toremifene on bone biochemistry and bone mineral density in postmenopausal breast cancer patients. J Clin Endocrinol Metab 1998; 83: 1158–62PubMedCrossRef
49.
go back to reference Weinstein RS, Parfitt AM, Marcus R, et al. Effects of raloxifene, hormone replacement therapy, and placebo on bone turnover in postmenopausal women. Osteoporos Int 2003; 14: 814–22PubMedCrossRef Weinstein RS, Parfitt AM, Marcus R, et al. Effects of raloxifene, hormone replacement therapy, and placebo on bone turnover in postmenopausal women. Osteoporos Int 2003; 14: 814–22PubMedCrossRef
50.
go back to reference Prestwood KM, Gunness M, Muchmore DB, et al. A comparison of the effects of raloxifene and estrogen on bone in postmenopausal women. J Clin Endocrinol Metab 2000 Jun; 85(6): 2197–202PubMedCrossRef Prestwood KM, Gunness M, Muchmore DB, et al. A comparison of the effects of raloxifene and estrogen on bone in postmenopausal women. J Clin Endocrinol Metab 2000 Jun; 85(6): 2197–202PubMedCrossRef
51.
go back to reference Ravn P, Nielsen TF, Christiansen C. What can be learned from the levormeloxifene experience? Acta Obstet Gynecol Scand 2006; 85(2): 135–42PubMedCrossRef Ravn P, Nielsen TF, Christiansen C. What can be learned from the levormeloxifene experience? Acta Obstet Gynecol Scand 2006; 85(2): 135–42PubMedCrossRef
52.
go back to reference Sadowski KK, Shott S, Brubaker L. A comparison of women with primary and recurrent pelvic prolapse. Am J Obstet Gynecol 1999; 180: 1415–8PubMedCrossRef Sadowski KK, Shott S, Brubaker L. A comparison of women with primary and recurrent pelvic prolapse. Am J Obstet Gynecol 1999; 180: 1415–8PubMedCrossRef
53.
go back to reference Goldstein SR, Nanavati N. Adverse events that are associated with the selective estrogen receptor modulator levormeloxifene in an aborted phase III osteoporosis treatment study. Am J Obstet Gynecol 2002; 187: 521–7PubMedCrossRef Goldstein SR, Nanavati N. Adverse events that are associated with the selective estrogen receptor modulator levormeloxifene in an aborted phase III osteoporosis treatment study. Am J Obstet Gynecol 2002; 187: 521–7PubMedCrossRef
54.
go back to reference Goss PE, Qi S, Cheung AM, et al. The selective estrogen receptor modulator SCH 57068 prevents bone loss, reduces serum cholesterol and blocks estrogen-induced uterine hypertrophy in ovariectomized rats. J Steroid Biochem Mol Biol 2004 Sep; 92 (1–2): 79–87CrossRef Goss PE, Qi S, Cheung AM, et al. The selective estrogen receptor modulator SCH 57068 prevents bone loss, reduces serum cholesterol and blocks estrogen-induced uterine hypertrophy in ovariectomized rats. J Steroid Biochem Mol Biol 2004 Sep; 92 (1–2): 79–87CrossRef
55.
go back to reference Narayana Murthy PS, Sengupta S, Sharma S, et al. Effect of ormeloxifene on ovariectomy-induced bone resorption, osteo-clast differentiation and apoptosis and TGF beta-3 expression. J Steroid Biochem Mol Biol 2006; 100(4–5): 117–28PubMedCrossRef Narayana Murthy PS, Sengupta S, Sharma S, et al. Effect of ormeloxifene on ovariectomy-induced bone resorption, osteo-clast differentiation and apoptosis and TGF beta-3 expression. J Steroid Biochem Mol Biol 2006; 100(4–5): 117–28PubMedCrossRef
56.
go back to reference Gennari L. Ospemifene (Hormos). Curr Opin Investig Drugs 2004 Apr; 5(4): 448–55PubMed Gennari L. Ospemifene (Hormos). Curr Opin Investig Drugs 2004 Apr; 5(4): 448–55PubMed
57.
go back to reference Willson TM, Norris JD, Wagner BL, et al. Dissection of the molecular mechanism of action of GW5638, a novel estrogen receptor ligand, provides insights into the role of estrogen receptor in bone. Endocrinology 1997; 138(9): 3901–11PubMedCrossRef Willson TM, Norris JD, Wagner BL, et al. Dissection of the molecular mechanism of action of GW5638, a novel estrogen receptor ligand, provides insights into the role of estrogen receptor in bone. Endocrinology 1997; 138(9): 3901–11PubMedCrossRef
58.
go back to reference Qu Q, Harkonen PL, Vaananen HK. Comparative effects of estrogen and antiestrogens on differentiation of osteoblasts in mouse bone marrow culture. J Cell Biochem 1999; 73(4): 500–7PubMedCrossRef Qu Q, Harkonen PL, Vaananen HK. Comparative effects of estrogen and antiestrogens on differentiation of osteoblasts in mouse bone marrow culture. J Cell Biochem 1999; 73(4): 500–7PubMedCrossRef
59.
go back to reference Parikka V, Lehenkari P, Harkonen PL, et al. The effect of two selective estrogens raloxifene and FC1271a on osteoclast survival and resorption in vitro [abstract]. Bone 1998; 23Suppl. 5: S552 Parikka V, Lehenkari P, Harkonen PL, et al. The effect of two selective estrogens raloxifene and FC1271a on osteoclast survival and resorption in vitro [abstract]. Bone 1998; 23Suppl. 5: S552
60.
go back to reference Qiang Q, Zhengt H, Dahlund J, et al. Selective estrogenic effects of a novel triphenylethylene compound, FC1271a, on bone, cholesterol levels and reproductive tissues in intact and ovariectomized rats. Endocrinology 2000; 141(2): 809–20CrossRef Qiang Q, Zhengt H, Dahlund J, et al. Selective estrogenic effects of a novel triphenylethylene compound, FC1271a, on bone, cholesterol levels and reproductive tissues in intact and ovariectomized rats. Endocrinology 2000; 141(2): 809–20CrossRef
61.
go back to reference Taras TL, Wurz GT, DeGregorio MW. In vitro and in vivo biologic effects of ospemifene (FC-1271a) in breast cancer. J Steroid Biochem Mol Biol 2001; 77(4–5): 271–9PubMedCrossRef Taras TL, Wurz GT, DeGregorio MW. In vitro and in vivo biologic effects of ospemifene (FC-1271a) in breast cancer. J Steroid Biochem Mol Biol 2001; 77(4–5): 271–9PubMedCrossRef
62.
go back to reference Hellmann-Blumberg U, Taras TL, Wurz GT, et al. Genotoxic effects of the novel mixed antiestrogen FC-1271a in comparison to tamoxifen and toremifene. Breast Cancer Res Treat 2000; 60(1): 63–70PubMedCrossRef Hellmann-Blumberg U, Taras TL, Wurz GT, et al. Genotoxic effects of the novel mixed antiestrogen FC-1271a in comparison to tamoxifen and toremifene. Breast Cancer Res Treat 2000; 60(1): 63–70PubMedCrossRef
63.
go back to reference DeGregorio MW, Wurz GT, Taras TL, et al. Pharmacokinetics of (deaminohydroxy) toremifene in humans: a new, selective estrogen-receptor modulator. Eur J Clin Pharmacol 2000; 56(6–7): 469–75PubMedCrossRef DeGregorio MW, Wurz GT, Taras TL, et al. Pharmacokinetics of (deaminohydroxy) toremifene in humans: a new, selective estrogen-receptor modulator. Eur J Clin Pharmacol 2000; 56(6–7): 469–75PubMedCrossRef
64.
go back to reference Olavi Y, Bruno C, Kaija H, et al. Effects of ospemifene, a novel SERM, on vascular markers and function in healthy, postmenopausal women. Menopause 2003; 10(5): 440–7CrossRef Olavi Y, Bruno C, Kaija H, et al. Effects of ospemifene, a novel SERM, on vascular markers and function in healthy, postmenopausal women. Menopause 2003; 10(5): 440–7CrossRef
65.
go back to reference Eeva Marja R, Jorma H, Kaija H, et al. Effects of ospemifene, a novel SERM, on hormones, genital tract, climacteric symptoms, and quality of life in postmenopausal women: a double-blind, randomized trial. Menopause 2003; 10(5): 433–9CrossRef Eeva Marja R, Jorma H, Kaija H, et al. Effects of ospemifene, a novel SERM, on hormones, genital tract, climacteric symptoms, and quality of life in postmenopausal women: a double-blind, randomized trial. Menopause 2003; 10(5): 433–9CrossRef
66.
go back to reference Voipio SK, Komi J, Halonen K, et al. Effects of ospemifene (FC-1271a) on uterine endometrium, vaginal maturation index, and hormonal status in healthy postmenopausal women. Maturitas 2002; 43(3): 207–14PubMedCrossRef Voipio SK, Komi J, Halonen K, et al. Effects of ospemifene (FC-1271a) on uterine endometrium, vaginal maturation index, and hormonal status in healthy postmenopausal women. Maturitas 2002; 43(3): 207–14PubMedCrossRef
67.
go back to reference Komi J, Lankinen KS, DeGregorio M, et al. Effects of ospemifene and raloxifene on biochemical markers of bone turnover in postmenopausal women. J Bone Miner Metab 2006; 24(4): 314–8PubMedCrossRef Komi J, Lankinen KS, DeGregorio M, et al. Effects of ospemifene and raloxifene on biochemical markers of bone turnover in postmenopausal women. J Bone Miner Metab 2006; 24(4): 314–8PubMedCrossRef
68.
go back to reference Komi J, Heikkinen J, Rutanen EM, et al. Effects of ospemifene, a novel SERM, on biochemical markers of bone turnover in healthy postmenopausal women. Gynecol Endocrinol 2004 Mar; 18(3): 152–8PubMedCrossRef Komi J, Heikkinen J, Rutanen EM, et al. Effects of ospemifene, a novel SERM, on biochemical markers of bone turnover in healthy postmenopausal women. Gynecol Endocrinol 2004 Mar; 18(3): 152–8PubMedCrossRef
69.
go back to reference Komi J, Lankinen KS, Harkonen P, et al. Effects of ospemifene and raloxifene on hormonal status, lipids, genital tract, and tolerability in postmenopausal women. Menopause 2005 Mar; 12(2): 202–9PubMedCrossRef Komi J, Lankinen KS, Harkonen P, et al. Effects of ospemifene and raloxifene on hormonal status, lipids, genital tract, and tolerability in postmenopausal women. Menopause 2005 Mar; 12(2): 202–9PubMedCrossRef
72.
go back to reference Namba R, Young LJ, Maglione JE, et al. Selective estrogen receptor modulators inhibit growth and progression of premalignant lesions in a mouse model of ductal carcinoma in situ. Breast Cancer Res 2005; 7(6): R881–9PubMedCrossRef Namba R, Young LJ, Maglione JE, et al. Selective estrogen receptor modulators inhibit growth and progression of premalignant lesions in a mouse model of ductal carcinoma in situ. Breast Cancer Res 2005; 7(6): R881–9PubMedCrossRef
73.
go back to reference Wurz GT, Read KC, Marchisano-Karpman C, et al. Ospemifene inhibits the growth of dimethylbenzanthracene-induced mammary tumors in Sencar mice. J Steroid Biochem Mol Biol 2005 Nov; 97(3): 230–40PubMedCrossRef Wurz GT, Read KC, Marchisano-Karpman C, et al. Ospemifene inhibits the growth of dimethylbenzanthracene-induced mammary tumors in Sencar mice. J Steroid Biochem Mol Biol 2005 Nov; 97(3): 230–40PubMedCrossRef
74.
go back to reference Gennari L. Lasofoxifene (Pfizer). Curr Opin Investig Drugs 2005 Oct; 6(10): 1067–78PubMed Gennari L. Lasofoxifene (Pfizer). Curr Opin Investig Drugs 2005 Oct; 6(10): 1067–78PubMed
75.
go back to reference Gennari L. Lasofoxifene: a new type of selective estrogen receptor modulator for the treatment of osteoporosis. Drugs Today (Barc) 2006 Jun; 42(6): 355–67CrossRef Gennari L. Lasofoxifene: a new type of selective estrogen receptor modulator for the treatment of osteoporosis. Drugs Today (Barc) 2006 Jun; 42(6): 355–67CrossRef
76.
go back to reference Gennari L, Merlotti D, Martini G, et al. Lasofoxifene: a third-generation selective estrogen receptor modulator for the prevention and treatment of osteoporosis. Expert Opin Investig Drugs 2006 Sep; 15(9): 1091–103PubMedCrossRef Gennari L, Merlotti D, Martini G, et al. Lasofoxifene: a third-generation selective estrogen receptor modulator for the prevention and treatment of osteoporosis. Expert Opin Investig Drugs 2006 Sep; 15(9): 1091–103PubMedCrossRef
77.
go back to reference Rosati RL, Da Silva Jardine P, Cameron KO, et al. Discovery and preclinical pharmacology of a novel, potent, nonsteroidal estrogen receptor agonist/antagonist, CP-336156, a diarylte-trahydronaphthalene. J Med Chem 1998; 41: 2928–31PubMedCrossRef Rosati RL, Da Silva Jardine P, Cameron KO, et al. Discovery and preclinical pharmacology of a novel, potent, nonsteroidal estrogen receptor agonist/antagonist, CP-336156, a diarylte-trahydronaphthalene. J Med Chem 1998; 41: 2928–31PubMedCrossRef
78.
go back to reference Cameron K. Discovery of CP-336156, a potent estrogen agonist [abstract]. 219th ACS Meeting; 2000 Mar 26–30; San Francisco, MEDI 326 Cameron K. Discovery of CP-336156, a potent estrogen agonist [abstract]. 219th ACS Meeting; 2000 Mar 26–30; San Francisco, MEDI 326
79.
go back to reference Yang X, Reinhold AR, Rosati RL, et al. Enzyme-catalyzed asymmetric deacylation for the preparation of lasofoxifene (CP-336156), a selective estrogen receptor modulator. Org Lett 2000; 2: 4025–7PubMedCrossRef Yang X, Reinhold AR, Rosati RL, et al. Enzyme-catalyzed asymmetric deacylation for the preparation of lasofoxifene (CP-336156), a selective estrogen receptor modulator. Org Lett 2000; 2: 4025–7PubMedCrossRef
80.
go back to reference Harris H, Bapat AR, Gonder DS, et al. The ligand binding profiles of estrogen receptors α and β are species dependent. Steroids 2002; 67: 379–84PubMedCrossRef Harris H, Bapat AR, Gonder DS, et al. The ligand binding profiles of estrogen receptors α and β are species dependent. Steroids 2002; 67: 379–84PubMedCrossRef
81.
go back to reference Katzenellenbogen JA. D-1,2-Dyaril-3,4-dihydronaphthalenes: photofluorogenic ligands for the estrogen receptor. J Steroid Biochem 1985; 23: 929–37PubMedCrossRef Katzenellenbogen JA. D-1,2-Dyaril-3,4-dihydronaphthalenes: photofluorogenic ligands for the estrogen receptor. J Steroid Biochem 1985; 23: 929–37PubMedCrossRef
82.
go back to reference Ke HZ, Paralkar VM, Grasser WA. Effects of CP-336, 156, a new, nonsteroidal estrogen agonist/antagonist, on bone, serum cholesterol, uterus and body composition in rat models. Endocrinology 1998; 139: 2068–76PubMedCrossRef Ke HZ, Paralkar VM, Grasser WA. Effects of CP-336, 156, a new, nonsteroidal estrogen agonist/antagonist, on bone, serum cholesterol, uterus and body composition in rat models. Endocrinology 1998; 139: 2068–76PubMedCrossRef
83.
go back to reference Ke HZ, Qi H, Chidsey-Frink KL, et al. Effects of different dose regimens of lasofoxifene (CP-336, 156) in preventing bone loss in ovariectomized rats [abstract no. SA413]. J Bone Miner Res 2000; 15Suppl. S1: S310 Ke HZ, Qi H, Chidsey-Frink KL, et al. Effects of different dose regimens of lasofoxifene (CP-336, 156) in preventing bone loss in ovariectomized rats [abstract no. SA413]. J Bone Miner Res 2000; 15Suppl. S1: S310
84.
go back to reference Ke HZ, Foley GL, Simmons HA, et al. Long-term treatment of lasofoxifene preserves bone mass and bone strength and does not adversely affect the uterus in ovariectomized rats. Endocrinology 2004; 145: 1996–2005PubMedCrossRef Ke HZ, Foley GL, Simmons HA, et al. Long-term treatment of lasofoxifene preserves bone mass and bone strength and does not adversely affect the uterus in ovariectomized rats. Endocrinology 2004; 145: 1996–2005PubMedCrossRef
85.
go back to reference Ke HZ, Qi H, Crawford DT, et al. Lasofoxifene (CP-336-156), a selective estrogen receptor modulator, prevents bone loss induced by aging and orchidectomy in the adult rat. Endocrinology 2000; 141: 1338–44PubMedCrossRef Ke HZ, Qi H, Crawford DT, et al. Lasofoxifene (CP-336-156), a selective estrogen receptor modulator, prevents bone loss induced by aging and orchidectomy in the adult rat. Endocrinology 2000; 141: 1338–44PubMedCrossRef
86.
go back to reference Ke HZ, Qi H, Chidsey-Frink KL, et al. Lasofoxifene (CP-336,156) protects against the age-related changes in bone mass, bone strength, and total serum cholesterol in intact aged male rats. J Bone Miner Res 2001; 16: 765–73PubMedCrossRef Ke HZ, Qi H, Chidsey-Frink KL, et al. Lasofoxifene (CP-336,156) protects against the age-related changes in bone mass, bone strength, and total serum cholesterol in intact aged male rats. J Bone Miner Res 2001; 16: 765–73PubMedCrossRef
87.
go back to reference Kharode YP, Green PD, Marzolf JT, et al. Comparison of the effects of bazedoxifene, raloxifene, lasofoxifene and risedronate, co-treatment on h-PTH-induced reversal of established osteopenia in ovariectomized rats [abstract no. SU387]. J Bone Miner Res 2003; 18Suppl. S2: S273 Kharode YP, Green PD, Marzolf JT, et al. Comparison of the effects of bazedoxifene, raloxifene, lasofoxifene and risedronate, co-treatment on h-PTH-induced reversal of established osteopenia in ovariectomized rats [abstract no. SU387]. J Bone Miner Res 2003; 18Suppl. S2: S273
88.
go back to reference Chesworth R, Zawistoski MP, Lefker BA, et al. Tetrahydroiso-quinolines as subtype selective estrogen agonists/antagonists. Bioorg Med Chem Lett 2004; 14: 2729–33PubMedCrossRef Chesworth R, Zawistoski MP, Lefker BA, et al. Tetrahydroiso-quinolines as subtype selective estrogen agonists/antagonists. Bioorg Med Chem Lett 2004; 14: 2729–33PubMedCrossRef
89.
go back to reference Cohen LA, Pittman B, Wang CX, et al. LAS, a novel selective estrogen receptor modulator with chemopreventive and therapeutic activity in the N-nitroso-N-methylurea-induced rat mammary tumor model. Cancer Res 2001; 61: 8683–8PubMed Cohen LA, Pittman B, Wang CX, et al. LAS, a novel selective estrogen receptor modulator with chemopreventive and therapeutic activity in the N-nitroso-N-methylurea-induced rat mammary tumor model. Cancer Res 2001; 61: 8683–8PubMed
90.
go back to reference McClung M, Portman D, Emkey R, et al. Comparison of the extraskeletal effects of lasofoxifene and raloxifene [abstract]. J Bone Miner Res 2004; 19(S1): SA423 McClung M, Portman D, Emkey R, et al. Comparison of the extraskeletal effects of lasofoxifene and raloxifene [abstract]. J Bone Miner Res 2004; 19(S1): SA423
91.
go back to reference Portman DJ, Moffett AH, Bachman GA, et al. Lasofoxifene, a selective estrogen receptor modulator, improves objective measures of vaginal atrophy. Obstet Gynecol 2004; 103(4): 25S–6S Portman DJ, Moffett AH, Bachman GA, et al. Lasofoxifene, a selective estrogen receptor modulator, improves objective measures of vaginal atrophy. Obstet Gynecol 2004; 103(4): 25S–6S
92.
go back to reference Davidson M, Moffett A, Welty F, et al. Extraskeletal effects of lasofoxifene on postmenopausal women [abstract]. J Bone Miner Res 2005; 20(S1): SA428 Davidson M, Moffett A, Welty F, et al. Extraskeletal effects of lasofoxifene on postmenopausal women [abstract]. J Bone Miner Res 2005; 20(S1): SA428
93.
go back to reference McClung MR, Siris E, Cummings S, et al. Prevention of bone loss in postmenopausal women treated with lasofoxifene compared with raloxifene. Menopause 2006 May–Jun; 13(3): 377–86PubMedCrossRef McClung MR, Siris E, Cummings S, et al. Prevention of bone loss in postmenopausal women treated with lasofoxifene compared with raloxifene. Menopause 2006 May–Jun; 13(3): 377–86PubMedCrossRef
94.
go back to reference Day W, Martel J, Lee A. Lasofoxifene phase 2 dose response analysis in postmenopausal women [abstract]. J Bone Miner Res 2005; 20(S1): M385 Day W, Martel J, Lee A. Lasofoxifene phase 2 dose response analysis in postmenopausal women [abstract]. J Bone Miner Res 2005; 20(S1): M385
95.
go back to reference Moffett AH, Ettinger M, Bolognese M, et al. Lasofoxifene, a next generation SERM, is effective in preventing loss of BMD and reducing LDL-C in postmenopausal women [abstract]. J Bone Miner Res 2004; 19(S1): SA426 Moffett AH, Ettinger M, Bolognese M, et al. Lasofoxifene, a next generation SERM, is effective in preventing loss of BMD and reducing LDL-C in postmenopausal women [abstract]. J Bone Miner Res 2004; 19(S1): SA426
96.
go back to reference McClung M, Omizo M, Weiss S, et al. Comparison of lasofoxifene and raloxifene for the prevention of bone loss in postmenopausal women [abstract]. J Bone Miner Res 2004; 19(S1): SA424 McClung M, Omizo M, Weiss S, et al. Comparison of lasofoxifene and raloxifene for the prevention of bone loss in postmenopausal women [abstract]. J Bone Miner Res 2004; 19(S1): SA424
97.
go back to reference McClung M, Siris E, Cummings S, et al. Lasofoxifene increased BMD of the spine and hip and decreased bone turnover markers in postmenopausal women with low or normal BMD [abstract]. J Bone Miner Res 2005; 20(S1): F429 McClung M, Siris E, Cummings S, et al. Lasofoxifene increased BMD of the spine and hip and decreased bone turnover markers in postmenopausal women with low or normal BMD [abstract]. J Bone Miner Res 2005; 20(S1): F429
98.
go back to reference Lee A, Radecki D, Wolter K, et al. Lasofoxifene phase 2 and phase 3 clinical trial design and strategy [abstract]. J Bone Miner Res 2005; 20(S1): M384 Lee A, Radecki D, Wolter K, et al. Lasofoxifene phase 2 and phase 3 clinical trial design and strategy [abstract]. J Bone Miner Res 2005; 20(S1): M384
99.
go back to reference Ligand earns milestone from Pfizer as lasofoxifene enters phase II for osteoporosis: first of three late-stage SERM products advancing prospects of future royalties [press release]. Ligand Pharmaceuticals International Inc., 2000 Sep 26 Ligand earns milestone from Pfizer as lasofoxifene enters phase II for osteoporosis: first of three late-stage SERM products advancing prospects of future royalties [press release]. Ligand Pharmaceuticals International Inc., 2000 Sep 26
100.
go back to reference Guidelines for preclinical evaluation and clinical trials in osteoporosis. Geneva: World Health Organization, 1998: 1–74 Guidelines for preclinical evaluation and clinical trials in osteoporosis. Geneva: World Health Organization, 1998: 1–74
101.
go back to reference Helvering LM, Adrian MD, Geiser AG, et al. Differential effects of estrogen and raloxifene on messenger RNA and matrix metalloproteinase 2 activity in rat uterus. Biol Reprod 2005; 72: 830–41PubMedCrossRef Helvering LM, Adrian MD, Geiser AG, et al. Differential effects of estrogen and raloxifene on messenger RNA and matrix metalloproteinase 2 activity in rat uterus. Biol Reprod 2005; 72: 830–41PubMedCrossRef
102.
go back to reference Curry TE, Osteen KG. The matrix metalloproteinase system: changes, regulation, and impact throughout the ovarian and uterine reproductive cycle. Endocr Rev 2003; 24: 428–65PubMedCrossRef Curry TE, Osteen KG. The matrix metalloproteinase system: changes, regulation, and impact throughout the ovarian and uterine reproductive cycle. Endocr Rev 2003; 24: 428–65PubMedCrossRef
103.
go back to reference Gruber C, Gruber D. Bazedoxifene (Wyeth). Curr Opin Investig Drugs 2004 Oct; 5(10): 1086–93PubMed Gruber C, Gruber D. Bazedoxifene (Wyeth). Curr Opin Investig Drugs 2004 Oct; 5(10): 1086–93PubMed
104.
go back to reference Miller CP, Collini MD, Tran BD. Design, synthesis, and preclinical characterization of novel, highly selective indole estrogens. J Med Chem 2001 May 24; 44(11): 1654–7PubMedCrossRef Miller CP, Collini MD, Tran BD. Design, synthesis, and preclinical characterization of novel, highly selective indole estrogens. J Med Chem 2001 May 24; 44(11): 1654–7PubMedCrossRef
105.
go back to reference Komm BS, Kharode YP, Bodine PV. Bazedoxifene acetate: a selective estrogen receptor modulator with improved selectivity. Endocrinology 2005 Sep; 146(9): 3999–4008PubMedCrossRef Komm BS, Kharode YP, Bodine PV. Bazedoxifene acetate: a selective estrogen receptor modulator with improved selectivity. Endocrinology 2005 Sep; 146(9): 3999–4008PubMedCrossRef
106.
go back to reference von Angerer E, Prekajac J, Strohmeier J. 2-Phenylindoles: relationship between structure, estrogen receptor affinity and mammary tumor inhibiting activity in the rat. J Med Chem 1984; 27(11): 1439–47CrossRef von Angerer E, Prekajac J, Strohmeier J. 2-Phenylindoles: relationship between structure, estrogen receptor affinity and mammary tumor inhibiting activity in the rat. J Med Chem 1984; 27(11): 1439–47CrossRef
107.
go back to reference Black LJ, Sato M, Rowley ER, et al. Raloxifene (LY139481 HCI) prevents bone loss and reduces serum cholesterol without causing uterine hypertrophy in ovariectomized rats. J Clin Invest 1994; 93: 63–9PubMedCrossRef Black LJ, Sato M, Rowley ER, et al. Raloxifene (LY139481 HCI) prevents bone loss and reduces serum cholesterol without causing uterine hypertrophy in ovariectomized rats. J Clin Invest 1994; 93: 63–9PubMedCrossRef
108.
go back to reference Smith SY, Minck D, Jolette J, et al. Bazedoxifene prevents ovariectomy-induced bone loss in the Cynomolgus monkey [abstract no. SA431]. J Bone Miner Res 2005; 20Suppl. S1: S174 Smith SY, Minck D, Jolette J, et al. Bazedoxifene prevents ovariectomy-induced bone loss in the Cynomolgus monkey [abstract no. SA431]. J Bone Miner Res 2005; 20Suppl. S1: S174
109.
go back to reference Komm BS, Kharode Y, Bodine P, et al. Bazedoxifene + conjugated estrogens: a balanced combination to provide optimal estrogenic “safety” and efficacy [abstract no. SU385]. J Bone Miner Res 2003; 18Suppl. S2: S272 Komm BS, Kharode Y, Bodine P, et al. Bazedoxifene + conjugated estrogens: a balanced combination to provide optimal estrogenic “safety” and efficacy [abstract no. SU385]. J Bone Miner Res 2003; 18Suppl. S2: S272
110.
go back to reference Komm BS, Kharode Y, Bodine P, et al. Combining a SERM with conjugated estrogens (CE) to improve the SERM profile: not all SERMs may succeed [abstract no. SU386]. J Bone Miner Res 2003 Sep 25; 18Suppl. S2: S273 Komm BS, Kharode Y, Bodine P, et al. Combining a SERM with conjugated estrogens (CE) to improve the SERM profile: not all SERMs may succeed [abstract no. SU386]. J Bone Miner Res 2003 Sep 25; 18Suppl. S2: S273
111.
go back to reference Morii H. American Society for Bone and Mineral Research 22nd Annual Meeting (Part III), Osteoporosis Drugs; 2000 Sep 22–26; Toronto. IDdb Meeting Report 2000 Sep 22–26 Morii H. American Society for Bone and Mineral Research 22nd Annual Meeting (Part III), Osteoporosis Drugs; 2000 Sep 22–26; Toronto. IDdb Meeting Report 2000 Sep 22–26
112.
go back to reference Chandrasekaran A, Ermer J, McKeand W, et al. Bazedoxifene acetate metabolic disposition in healthy postmenopausal women. Clin Pharmacol Ther 2003; 73(2): 47CrossRef Chandrasekaran A, Ermer J, McKeand W, et al. Bazedoxifene acetate metabolic disposition in healthy postmenopausal women. Clin Pharmacol Ther 2003; 73(2): 47CrossRef
113.
go back to reference Ermer J, McKeand W, Sullivan P, et al. Bazedoxifene acetate dose proportionality in healthy postmenopausal women [abstract]. Clin Pharmacol Ther 2003; 73(2): 46CrossRef Ermer J, McKeand W, Sullivan P, et al. Bazedoxifene acetate dose proportionality in healthy postmenopausal women [abstract]. Clin Pharmacol Ther 2003; 73(2): 46CrossRef
114.
go back to reference Patat A, McKeand W, Baird Bellaire S, et al. Absolute/relative bioavailability of bazedoxifene acetate in healthy postmenopausal women [abstract]. Clin Pharmacol Ther 2003; 73(2): 43CrossRef Patat A, McKeand W, Baird Bellaire S, et al. Absolute/relative bioavailability of bazedoxifene acetate in healthy postmenopausal women [abstract]. Clin Pharmacol Ther 2003; 73(2): 43CrossRef
115.
go back to reference Ronkin S, Clarke L, Boudes P, et al. TSE-424, a novel tissue selective estrogen, reduces biochemical indices of bone metabolism in a dose related fashion [abstract no. SU437]. J Bone Miner Res 2001; 16Suppl. S1: S413 Ronkin S, Clarke L, Boudes P, et al. TSE-424, a novel tissue selective estrogen, reduces biochemical indices of bone metabolism in a dose related fashion [abstract no. SU437]. J Bone Miner Res 2001; 16Suppl. S1: S413
116.
go back to reference Ronkin S, Northington R, Baracat E, et al. Endometrial effects of bazedoxifene acetate, a novel selective estrogen receptor modulator, in postmenopausal women [published erratum appears in Obstet Gynecol 2005 Oct; 106 (4): 869]. Obstet Gynecol 2005 Jun; 105(6): 1397–404PubMedCrossRef Ronkin S, Northington R, Baracat E, et al. Endometrial effects of bazedoxifene acetate, a novel selective estrogen receptor modulator, in postmenopausal women [published erratum appears in Obstet Gynecol 2005 Oct; 106 (4): 869]. Obstet Gynecol 2005 Jun; 105(6): 1397–404PubMedCrossRef
118.
go back to reference Sato M, Turner CH, Wang T, et al. LY353381.HC1: a novel raloxifene analogue with improved SERM potency and efficacy in vivo. J Pharmacol Exp Ther 1998; 287: 1–7PubMed Sato M, Turner CH, Wang T, et al. LY353381.HC1: a novel raloxifene analogue with improved SERM potency and efficacy in vivo. J Pharmacol Exp Ther 1998; 287: 1–7PubMed
119.
go back to reference Munster PN. Arzoxifene: the development and clinical outcome of an ideal SERM. Expert Opin Investig Drugs 2006 Mar; 15(3): 317–26PubMedCrossRef Munster PN. Arzoxifene: the development and clinical outcome of an ideal SERM. Expert Opin Investig Drugs 2006 Mar; 15(3): 317–26PubMedCrossRef
120.
go back to reference Dodge JA, Lugar CW, Cho S, et al. Evaluation of the major metabolites of raloxifene as modulators of tissue selectivity. J Steroid Biochem Mol Biol 1997 Apr; 61(1–2): 97–106PubMedCrossRef Dodge JA, Lugar CW, Cho S, et al. Evaluation of the major metabolites of raloxifene as modulators of tissue selectivity. J Steroid Biochem Mol Biol 1997 Apr; 61(1–2): 97–106PubMedCrossRef
121.
go back to reference Grese TA, Sluka JP, Bryant HU, et al. Molecular determinants of tissue selectivity in estrogen receptor modulators. Proc Natl Acad Sci U S A 1997 Dec 9; 94(25): 14105–10PubMedCrossRef Grese TA, Sluka JP, Bryant HU, et al. Molecular determinants of tissue selectivity in estrogen receptor modulators. Proc Natl Acad Sci U S A 1997 Dec 9; 94(25): 14105–10PubMedCrossRef
122.
go back to reference Palkowitz AD, Glasebrook AL, Thrasher KJ, et al. Discovery and synthesis of [6-hydroxy-3-[4-[2-(l-piperidinyl)ethox-y]phenoxy]-2-(4-hydroxyphenyl)]benzo[b]thiophene: a novel, highly potent, selective estrogen receptor modulator. J Med Chem 1997 May 9; 40(10): 1407–16PubMedCrossRef Palkowitz AD, Glasebrook AL, Thrasher KJ, et al. Discovery and synthesis of [6-hydroxy-3-[4-[2-(l-piperidinyl)ethox-y]phenoxy]-2-(4-hydroxyphenyl)]benzo[b]thiophene: a novel, highly potent, selective estrogen receptor modulator. J Med Chem 1997 May 9; 40(10): 1407–16PubMedCrossRef
123.
go back to reference Bryant HU, Glasebrook AL, Yang NN, et al. An estrogen receptor basis for raloxifene action in bone. J Steroid Biochem Mol Biol 1999 Apr–Jun; 69(1–6): 37–44PubMedCrossRef Bryant HU, Glasebrook AL, Yang NN, et al. An estrogen receptor basis for raloxifene action in bone. J Steroid Biochem Mol Biol 1999 Apr–Jun; 69(1–6): 37–44PubMedCrossRef
124.
go back to reference Grese TA, Cho S, Finley DR, et al. Structure-activity relationships of selective estrogen receptor modulators: modifications to the 2-arylbenzothiophene core of raloxifene. J Med Chem 1997 Jan 17; 40(2): 146–67PubMedCrossRef Grese TA, Cho S, Finley DR, et al. Structure-activity relationships of selective estrogen receptor modulators: modifications to the 2-arylbenzothiophene core of raloxifene. J Med Chem 1997 Jan 17; 40(2): 146–67PubMedCrossRef
125.
go back to reference Grese TA, Pennington LD, Sluka JP, et al. Synthesis and pharmacology of conformationally restricted raloxifene analogues: highly potent selective estrogen receptor modulators. J Med Chem 1998 Apr 9; 41(8): 1272–83PubMedCrossRef Grese TA, Pennington LD, Sluka JP, et al. Synthesis and pharmacology of conformationally restricted raloxifene analogues: highly potent selective estrogen receptor modulators. J Med Chem 1998 Apr 9; 41(8): 1272–83PubMedCrossRef
126.
go back to reference Liu H, Liu J, van Breemen RB, et al. Bioactivation of the selective estrogen receptor modulator desmethylated arzoxifene to quinoids: 4′-fluoro substitution prevents quinoid formation. Chem Res Toxicol 2005; 18: 162–73PubMedCrossRef Liu H, Liu J, van Breemen RB, et al. Bioactivation of the selective estrogen receptor modulator desmethylated arzoxifene to quinoids: 4′-fluoro substitution prevents quinoid formation. Chem Res Toxicol 2005; 18: 162–73PubMedCrossRef
127.
go back to reference Freddie CT, Larsen SS, Bartholomaeussen M, et al. The effect of the new SERM arzoxifene on growth and gene expression in MCF-7 breast cancer cells. Mol Cell Endocrinol 2004 Apr 30; 219(1–2): 27–36PubMedCrossRef Freddie CT, Larsen SS, Bartholomaeussen M, et al. The effect of the new SERM arzoxifene on growth and gene expression in MCF-7 breast cancer cells. Mol Cell Endocrinol 2004 Apr 30; 219(1–2): 27–36PubMedCrossRef
128.
go back to reference Dardes RC, Bentrem D, O’Regan RM, et al. Effects of the new selective estrogen receptor modulator LY353381.HC1 (arzoxifene) on human endometrial cancer growth in athymic mice. Clin Cancer Res 2001 Dec; 7(12): 4149–55PubMed Dardes RC, Bentrem D, O’Regan RM, et al. Effects of the new selective estrogen receptor modulator LY353381.HC1 (arzoxifene) on human endometrial cancer growth in athymic mice. Clin Cancer Res 2001 Dec; 7(12): 4149–55PubMed
129.
go back to reference Detre S, Riddler S, Salter J, et al. Comparison of the selective estrogen receptor modulator arzoxifene (LY353381) with tamoxifen on tumor growth and biomarker expression in an MCF-7 human breast cancer xenograft model. Cancer Res 2003 Oct 1; 63(19): 6516–22PubMed Detre S, Riddler S, Salter J, et al. Comparison of the selective estrogen receptor modulator arzoxifene (LY353381) with tamoxifen on tumor growth and biomarker expression in an MCF-7 human breast cancer xenograft model. Cancer Res 2003 Oct 1; 63(19): 6516–22PubMed
130.
go back to reference Licun W, Tannock IF. Selective estrogen receptor modulators as inhibitors of repopulation of human breast cancer cell lines after chemotherapy. Clin Cancer Res 2003 Oct 1; 9(12): 4614–8PubMed Licun W, Tannock IF. Selective estrogen receptor modulators as inhibitors of repopulation of human breast cancer cell lines after chemotherapy. Clin Cancer Res 2003 Oct 1; 9(12): 4614–8PubMed
131.
go back to reference Suh N, Glasebrook AL, Palkowitz AD, et al. Arzoxifene, a new selective estrogen receptor modulator for chemoprevention of experimental breast cancer. Cancer Res 2001 Dec 1; 61(23): 8412–5PubMed Suh N, Glasebrook AL, Palkowitz AD, et al. Arzoxifene, a new selective estrogen receptor modulator for chemoprevention of experimental breast cancer. Cancer Res 2001 Dec 1; 61(23): 8412–5PubMed
132.
go back to reference Ma YL, Bryant HU, Zeng Q, et al. Long-term dosing of arzoxifene lowers cholesterol, reduces bone turnover, and preserves bone quality in ovariectomized rats. J Bone Miner Res 2002 Dec; 17(12): 2256–64PubMedCrossRef Ma YL, Bryant HU, Zeng Q, et al. Long-term dosing of arzoxifene lowers cholesterol, reduces bone turnover, and preserves bone quality in ovariectomized rats. J Bone Miner Res 2002 Dec; 17(12): 2256–64PubMedCrossRef
133.
go back to reference Sato M, Zeng GQ, Rowley E, et al. LY353381 x HCl: an improved benzothiophene analog with bone efficacy complementary to parathyroid hormone-(l-34). Endocrinology 1998 Nov; 139(11): 4642–51PubMedCrossRef Sato M, Zeng GQ, Rowley E, et al. LY353381 x HCl: an improved benzothiophene analog with bone efficacy complementary to parathyroid hormone-(l-34). Endocrinology 1998 Nov; 139(11): 4642–51PubMedCrossRef
134.
go back to reference Munster PN, Buzdar A, Dhingra K, et al. Phase I study of a third-generation selective estrogen receptor modulator, LY353381.HCL, in metastatic breast cancer. J Clin Oncol 2001 Apr 1; 19(7): 2002–9PubMed Munster PN, Buzdar A, Dhingra K, et al. Phase I study of a third-generation selective estrogen receptor modulator, LY353381.HCL, in metastatic breast cancer. J Clin Oncol 2001 Apr 1; 19(7): 2002–9PubMed
135.
go back to reference McMeekin D, Gordon A, Fowler J, et al. Phase II trial of arzoxifene, a selective estrogen response modulator, in patients with recurrent or advanced endometrial cancer. Gynecol Oncol 2003; 90(1): 64–9PubMedCrossRef McMeekin D, Gordon A, Fowler J, et al. Phase II trial of arzoxifene, a selective estrogen response modulator, in patients with recurrent or advanced endometrial cancer. Gynecol Oncol 2003; 90(1): 64–9PubMedCrossRef
136.
go back to reference Baselga J, Llombart-Cussac A, Bellet M, et al. Randomized, double-blind, multicenter trial comparing two doses of arzoxifene (LY353381) in hormone-sensitive advanced or metastatic breast cancer patients. Ann Oncol 2003 Sep; 14(9): 1383–90PubMedCrossRef Baselga J, Llombart-Cussac A, Bellet M, et al. Randomized, double-blind, multicenter trial comparing two doses of arzoxifene (LY353381) in hormone-sensitive advanced or metastatic breast cancer patients. Ann Oncol 2003 Sep; 14(9): 1383–90PubMedCrossRef
Metadata
Title
Selective Estrogen Receptor Modulators for Postmenopausal Osteoporosis
Current State of Development
Authors
Dr Luigi Gennari
Daniela Merlotti
Fabrizio Valleggi
Giuseppe Martini
Ranuccio Nuti
Publication date
01-05-2007
Publisher
Springer International Publishing
Published in
Drugs & Aging / Issue 5/2007
Print ISSN: 1170-229X
Electronic ISSN: 1179-1969
DOI
https://doi.org/10.2165/00002512-200724050-00002

Other articles of this Issue 5/2007

Drugs & Aging 5/2007 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.