메뉴 건너뛰기




Volumn 29, Issue 6, 2007, Pages 1116-1127

Clinical evaluation of novel bisphosphonate dosing regimens in osteoporosis: The role of comparative studies and implications for future studies

Author keywords

active comparator study; bisphosphonates; bridging study; monthly; study design; weekly

Indexed keywords

ALENDRONIC ACID; AMINO TERMINAL TELOPEPTIDE; BISPHOSPHONIC ACID DERIVATIVE; CARBOXY TERMINAL TELOPEPTIDE; COLLAGEN TYPE 1; IBANDRONIC ACID; RISEDRONIC ACID;

EID: 34547581275     PISSN: 01492918     EISSN: 1879114X     Source Type: Journal    
DOI: 10.1016/j.clinthera.2007.06.009     Document Type: Note
Times cited : (8)

References (62)
  • 1
    • 0004851872 scopus 로고    scopus 로고
    • Randomised trial of effect of alendronate on risk of fracture in women with existing vertebral fractures
    • for the Fracture Intervention Trial Research Group
    • for the Fracture Intervention Trial Research Group. Black D., Cummings S., Karpf D., et al. Randomised trial of effect of alendronate on risk of fracture in women with existing vertebral fractures. Lancet 348 (1996) 1535-1541
    • (1996) Lancet , vol.348 , pp. 1535-1541
    • Black, D.1    Cummings, S.2    Karpf, D.3
  • 2
    • 0036690206 scopus 로고    scopus 로고
    • The efficacy and tolerability of risedronate once a week for the treatment of postmenopausal osteoporosis
    • Brown J., Kendler D., McClung M., et al. The efficacy and tolerability of risedronate once a week for the treatment of postmenopausal osteoporosis. Calcif Tissue Int 71 (2002) 103-111
    • (2002) Calcif Tissue Int , vol.71 , pp. 103-111
    • Brown, J.1    Kendler, D.2    McClung, M.3
  • 3
    • 4544262219 scopus 로고    scopus 로고
    • Effects of oral ibandronate administered daily or intermittently on fracture risk in postmenopausal osteoporosis
    • for the Oral Ibandronate Osteoporosis Vertebral Fracture Trial in North America and Europe (BONE)
    • for the Oral Ibandronate Osteoporosis Vertebral Fracture Trial in North America and Europe (BONE). Chesnut III C., Skag A., Christiansen C., et al. Effects of oral ibandronate administered daily or intermittently on fracture risk in postmenopausal osteoporosis. J Bone Miner Res 19 (2004) 1241-1249
    • (2004) J Bone Miner Res , vol.19 , pp. 1241-1249
    • Chesnut III, C.1    Skag, A.2    Christiansen, C.3
  • 4
    • 0032583492 scopus 로고    scopus 로고
    • Effect of alendronate on risk of fracture in women with low bone density but without vertebral fractures: Results from the Fracture Intervention Trial
    • Cummings S., Black D., Thompson D., et al. Effect of alendronate on risk of fracture in women with low bone density but without vertebral fractures: Results from the Fracture Intervention Trial. JAMA 280 (1998) 2077-2082
    • (1998) JAMA , vol.280 , pp. 2077-2082
    • Cummings, S.1    Black, D.2    Thompson, D.3
  • 5
    • 4344580653 scopus 로고    scopus 로고
    • Daily and intermittent oral ibandronate normalize bone turnover and provide significant reduction in vertebral fracture risk: Results from the BONE study
    • Delmas P., Recker R., Chesnut III C., et al. Daily and intermittent oral ibandronate normalize bone turnover and provide significant reduction in vertebral fracture risk: Results from the BONE study. Osteoporos Int 15 (2004) 792-798
    • (2004) Osteoporos Int , vol.15 , pp. 792-798
    • Delmas, P.1    Recker, R.2    Chesnut III, C.3
  • 6
    • 0033552255 scopus 로고    scopus 로고
    • Effects of risedronate treatment on vertebral and nonvertebral fractures in women with postmenopausal osteoporosis: A randomized controlled trial
    • for the Vertebral Efficacy With Risedronate Therapy (VERT) Study Group
    • for the Vertebral Efficacy With Risedronate Therapy (VERT) Study Group. Harris S., Watts N., Genant H., et al. Effects of risedronate treatment on vertebral and nonvertebral fractures in women with postmenopausal osteoporosis: A randomized controlled trial. JAMA 282 (1999) 1344-1352
    • (1999) JAMA , vol.282 , pp. 1344-1352
    • Harris, S.1    Watts, N.2    Genant, H.3
  • 7
    • 0035253489 scopus 로고    scopus 로고
    • Effect of risedronate on the risk of hip fracture in elderly women
    • for the Hip Intervention Program Study Group
    • for the Hip Intervention Program Study Group. McClung M., Geusens P., Miller P., et al. Effect of risedronate on the risk of hip fracture in elderly women. N Engl J Med 344 (2001) 333-340
    • (2001) N Engl J Med , vol.344 , pp. 333-340
    • McClung, M.1    Geusens, P.2    Miller, P.3
  • 8
    • 22744433117 scopus 로고    scopus 로고
    • Monthly oral ibandronate therapy in postmenopausal osteoporosis: 1-Year results from the MOBILE study
    • Miller P., McClung M., Macovei L., et al. Monthly oral ibandronate therapy in postmenopausal osteoporosis: 1-Year results from the MOBILE study. J Bone Miner Res 20 (2005) 1315-1322
    • (2005) J Bone Miner Res , vol.20 , pp. 1315-1322
    • Miller, P.1    McClung, M.2    Macovei, L.3
  • 9
    • 0032896590 scopus 로고    scopus 로고
    • Multinational, placebo-controlled, randomized trial of the effects of alendronate on bone density and fracture risk in postmenopausal women with low bone mass: Results of the FOSIT study
    • for the Fosamax International Trial Study Group
    • for the Fosamax International Trial Study Group. Pols H., Felsenberg D., Hanley D., et al. Multinational, placebo-controlled, randomized trial of the effects of alendronate on bone density and fracture risk in postmenopausal women with low bone mass: Results of the FOSIT study. Osteoporos Int 9 (1999) 461-468
    • (1999) Osteoporos Int , vol.9 , pp. 461-468
    • Pols, H.1    Felsenberg, D.2    Hanley, D.3
  • 10
    • 12944291524 scopus 로고    scopus 로고
    • Randomized trial of the effects of risedronate on vertebral fractures in women with established postmenopausal osteoporosis
    • for the Vertebral Efficacy with Risedronate Therapy (VERT) Study Group
    • for the Vertebral Efficacy with Risedronate Therapy (VERT) Study Group. Reginster J., Minne H., Sorensen O., et al. Randomized trial of the effects of risedronate on vertebral fractures in women with established postmenopausal osteoporosis. Osteoporos Int 11 (2000) 83-91
    • (2000) Osteoporos Int , vol.11 , pp. 83-91
    • Reginster, J.1    Minne, H.2    Sorensen, O.3
  • 11
    • 0034097152 scopus 로고    scopus 로고
    • Therapeutic equivalence of alendronate 70 mg once-weekly and alendronate 10 mg daily in the treatment of osteoporosis
    • for the Alendronate Once-Weekly Study Group
    • for the Alendronate Once-Weekly Study Group. Schnitzer T., Bone H., Crepaldi G., et al. Therapeutic equivalence of alendronate 70 mg once-weekly and alendronate 10 mg daily in the treatment of osteoporosis. Aging (Milano) 12 (2000) 1-12
    • (2000) Aging (Milano) , vol.12 , pp. 1-12
    • Schnitzer, T.1    Bone, H.2    Crepaldi, G.3
  • 12
    • 12144289279 scopus 로고    scopus 로고
    • Ten years' experience with alendronate for osteoporosis in postmenopausal women
    • for the Alendronate Phase III Osteoporosis Treatment Study Group
    • for the Alendronate Phase III Osteoporosis Treatment Study Group. Bone H., Hosking D., Devogelaer J., et al. Ten years' experience with alendronate for osteoporosis in postmenopausal women. N Engl J Med 350 (2004) 1189-1199
    • (2004) N Engl J Med , vol.350 , pp. 1189-1199
    • Bone, H.1    Hosking, D.2    Devogelaer, J.3
  • 13
    • 3042689740 scopus 로고    scopus 로고
    • Alendronate in the prevention of osteoporosis: 7-Year follow-up
    • Sambrook P., Rodriguez J., Wasnich R., et al. Alendronate in the prevention of osteoporosis: 7-Year follow-up. Osteoporos Int 15 (2004) 483-488
    • (2004) Osteoporos Int , vol.15 , pp. 483-488
    • Sambrook, P.1    Rodriguez, J.2    Wasnich, R.3
  • 14
    • 12944312227 scopus 로고    scopus 로고
    • Five years of treatment with risedronate and its effects on bone safety in women with postmenopausal osteoporosis
    • Ste-Marie L., Sod E., Johnson T., and Chines A. Five years of treatment with risedronate and its effects on bone safety in women with postmenopausal osteoporosis. Calcif Tissue Int 75 (2004) 469-476
    • (2004) Calcif Tissue Int , vol.75 , pp. 469-476
    • Ste-Marie, L.1    Sod, E.2    Johnson, T.3    Chines, A.4
  • 15
    • 0036860290 scopus 로고    scopus 로고
    • Patient preference for once-weekly alendronate 70 mg versus once-daily alendronate 10 mg: A multicenter, randomized, open-label, crossover study
    • Simon J., Lewiecki E., Smith M., et al. Patient preference for once-weekly alendronate 70 mg versus once-daily alendronate 10 mg: A multicenter, randomized, open-label, crossover study. Clin Ther 24 (2002) 1871-1886
    • (2002) Clin Ther , vol.24 , pp. 1871-1886
    • Simon, J.1    Lewiecki, E.2    Smith, M.3
  • 16
    • 2942659309 scopus 로고    scopus 로고
    • Patients with osteoporosis prefer once weekly to once daily dosing with alendronate
    • Kendler D., Kung A., Fuleihan Gel H., et al. Patients with osteoporosis prefer once weekly to once daily dosing with alendronate. Maturitas 48 (2004) 243-251
    • (2004) Maturitas , vol.48 , pp. 243-251
    • Kendler, D.1    Kung, A.2    Fuleihan Gel, H.3
  • 17
    • 27744606747 scopus 로고    scopus 로고
    • Bisphosphonate dosing preferences in women with postmenopausal osteoporosis: A study
    • Simon J., Beusterien K., Hebborn A., et al. Bisphosphonate dosing preferences in women with postmenopausal osteoporosis: A study. Female Patient 30 (2005) 31-36
    • (2005) Female Patient , vol.30 , pp. 31-36
    • Simon, J.1    Beusterien, K.2    Hebborn, A.3
  • 18
    • 29144523956 scopus 로고    scopus 로고
    • Patient preference for once-monthly ibandronate versus once-weekly alendronate in a randomized, open-label, cross-over trial: The Boniva Alendronate Trial in Osteoporosis (BALTO)
    • Emkey R., Koltun W., Beusterien K., et al. Patient preference for once-monthly ibandronate versus once-weekly alendronate in a randomized, open-label, cross-over trial: The Boniva Alendronate Trial in Osteoporosis (BALTO). Curr Med Res Opin 21 (2005) 1895-1903
    • (2005) Curr Med Res Opin , vol.21 , pp. 1895-1903
    • Emkey, R.1    Koltun, W.2    Beusterien, K.3
  • 19
    • 25444477545 scopus 로고    scopus 로고
    • Compliance and persistence with bisphosphonate dosing regimens among women with postmenopausal osteoporosis
    • Cramer J., Amonkar M., Hebborn A., and Altman R. Compliance and persistence with bisphosphonate dosing regimens among women with postmenopausal osteoporosis. Curr Med Res Opin 21 (2005) 1453-1460
    • (2005) Curr Med Res Opin , vol.21 , pp. 1453-1460
    • Cramer, J.1    Amonkar, M.2    Hebborn, A.3    Altman, R.4
  • 20
    • 21344464904 scopus 로고    scopus 로고
    • Effect of dosing frequency on bisphosphonate medication adherence in a large longitudinal cohort of women
    • Recker R., Gallagher R., and MacCosbe P. Effect of dosing frequency on bisphosphonate medication adherence in a large longitudinal cohort of women. Mayo Clin Proc 80 (2005) 856-861
    • (2005) Mayo Clin Proc , vol.80 , pp. 856-861
    • Recker, R.1    Gallagher, R.2    MacCosbe, P.3
  • 21
    • 33744774092 scopus 로고    scopus 로고
    • Determinants of persistence with bisphosphonates: A study in women with postmenopausal osteoporosis
    • Penning-van Beest F., Goettsch W., Erkens J., and Herings R. Determinants of persistence with bisphosphonates: A study in women with postmenopausal osteoporosis. Clin Ther 28 (2006) 236-242
    • (2006) Clin Ther , vol.28 , pp. 236-242
    • Penning-van Beest, F.1    Goettsch, W.2    Erkens, J.3    Herings, R.4
  • 22
    • 34547597888 scopus 로고    scopus 로고
    • Adherence to bisphosphonates (BPs) is associated with reduced fracture risk in women with postmenopausal osteoporosis (PMO)
    • Abstract P-75.
    • Abstract P-75. Siris E., Harris S., Silverman S., et al. Adherence to bisphosphonates (BPs) is associated with reduced fracture risk in women with postmenopausal osteoporosis (PMO). Menopause 12 (2005) 807
    • (2005) Menopause , vol.12 , pp. 807
    • Siris, E.1    Harris, S.2    Silverman, S.3
  • 23
    • 34547586251 scopus 로고    scopus 로고
    • www.wma.net/e/policy/b3.htm
  • 24
    • 34547609839 scopus 로고    scopus 로고
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. Guidance for industry: E 10 Choice of control group and related issues in clinical trials. Available at Accessed July 5, 2006.
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. Guidance for industry: E 10 Choice of control group and related issues in clinical trials. Available at. www.fda.gov/cber/gdlns/clincontr0501.pdf Accessed July 5, 2006.
  • 25
    • 0034687104 scopus 로고    scopus 로고
    • Are placebo-controlled clinical trials ethical or needed when alternative treatment exists [published correction appears in Ann Intern Med. 2000;133:754]
    • Simon R. Are placebo-controlled clinical trials ethical or needed when alternative treatment exists [published correction appears in Ann Intern Med. 2000;133:754]. Ann Intern Med 133 (2000) 474-475
    • (2000) Ann Intern Med , vol.133 , pp. 474-475
    • Simon, R.1
  • 26
    • 0034687072 scopus 로고    scopus 로고
    • Placebo-controlled trials and active-control trials in the evaluation of new treatments. Part 1: Ethical and scientific issues
    • Temple R., and Ellenberg S. Placebo-controlled trials and active-control trials in the evaluation of new treatments. Part 1: Ethical and scientific issues. Ann Intern Med 133 (2000) 455-463
    • (2000) Ann Intern Med , vol.133 , pp. 455-463
    • Temple, R.1    Ellenberg, S.2
  • 27
    • 0034687076 scopus 로고    scopus 로고
    • Placebo-controlled trials and active-control trials in the evaluation of new treatments. Part 2: Practical issues and specific cases
    • Ellenberg S., and Temple R. Placebo-controlled trials and active-control trials in the evaluation of new treatments. Part 2: Practical issues and specific cases. Ann Intern Med 133 (2000) 464-470
    • (2000) Ann Intern Med , vol.133 , pp. 464-470
    • Ellenberg, S.1    Temple, R.2
  • 28
    • 18244385014 scopus 로고    scopus 로고
    • The use of placebo-controlled and non-inferiority trials for the evaluation of new drugs in the treatment of postmenopausal osteoporosis
    • for the Group for the Respect of Ethics and Excellence in Science (GREES)
    • for the Group for the Respect of Ethics and Excellence in Science (GREES). Delmas P., Calvo G., Boers M., et al. The use of placebo-controlled and non-inferiority trials for the evaluation of new drugs in the treatment of postmenopausal osteoporosis. Osteoporos Int 13 (2002) 1-5
    • (2002) Osteoporos Int , vol.13 , pp. 1-5
    • Delmas, P.1    Calvo, G.2    Boers, M.3
  • 29
    • 0142122896 scopus 로고    scopus 로고
    • Is the use of placebo controls ethically permissible in clinical trials of agents intended to reduce fractures in osteoporosis?
    • Brody B., Dickey N., Ellenberg S., et al. Is the use of placebo controls ethically permissible in clinical trials of agents intended to reduce fractures in osteoporosis?. J Bone Miner Res 18 (2003) 1105-1109
    • (2003) J Bone Miner Res , vol.18 , pp. 1105-1109
    • Brody, B.1    Dickey, N.2    Ellenberg, S.3
  • 30
    • 0142122891 scopus 로고    scopus 로고
    • Ethical issues in the design of osteoporosis clinical trials: The state of the question
    • Heaney R. Ethical issues in the design of osteoporosis clinical trials: The state of the question. J Bone Miner Res 18 (2003) 1117-1120
    • (2003) J Bone Miner Res , vol.18 , pp. 1117-1120
    • Heaney, R.1
  • 31
    • 0142122890 scopus 로고    scopus 로고
    • Scientific and ethical issues in the use of placebo and active controls in clinical trials
    • Ellenberg S. Scientific and ethical issues in the use of placebo and active controls in clinical trials. J Bone Miner Res 18 (2003) 1121-1124
    • (2003) J Bone Miner Res , vol.18 , pp. 1121-1124
    • Ellenberg, S.1
  • 32
    • 0142027576 scopus 로고    scopus 로고
    • Study designs in osteoporosis
    • Temple R. Study designs in osteoporosis. J Bone Miner Res 18 (2003) 1129-1132
    • (2003) J Bone Miner Res , vol.18 , pp. 1129-1132
    • Temple, R.1
  • 33
    • 0142122885 scopus 로고    scopus 로고
    • Is it ethical to conduct placebo-controlled clinical trials in the development of new agents for osteoporosis? An industry perspective
    • Rosenblatt M. Is it ethical to conduct placebo-controlled clinical trials in the development of new agents for osteoporosis? An industry perspective. J Bone Miner Res 18 (2003) 1142-1145
    • (2003) J Bone Miner Res , vol.18 , pp. 1142-1145
    • Rosenblatt, M.1
  • 35
    • 29144508420 scopus 로고    scopus 로고
    • Recommendations for an update of the current (2001) regulatory requirements for registration of drugs to be used in the treatment of osteoporosis in postmenopausal women and in men
    • Reginster J., Abadie E., Delmas P., et al. Recommendations for an update of the current (2001) regulatory requirements for registration of drugs to be used in the treatment of osteoporosis in postmenopausal women and in men. Osteoporos Int 17 (2006) 1-7
    • (2006) Osteoporos Int , vol.17 , pp. 1-7
    • Reginster, J.1    Abadie, E.2    Delmas, P.3
  • 36
    • 0033566769 scopus 로고    scopus 로고
    • ICH Harmonised Tripartite Guideline. Statistical principles for clinical trials
    • International Conference on Harmonisation E9 Expert Working Group
    • International Conference on Harmonisation E9 Expert Working Group. ICH Harmonised Tripartite Guideline. Statistical principles for clinical trials. Stat Med 18 (1999) 1905-1942
    • (1999) Stat Med , vol.18 , pp. 1905-1942
  • 37
    • 34547555480 scopus 로고    scopus 로고
    • www.emea.eu.int/pdfs/human/ewp/055295.pdf
  • 38
    • 0033552264 scopus 로고    scopus 로고
    • Users' Guides to the Medical Literature: XIX. Applying clinical trial results B. Guidelines for determining whether a drug is exerting (more than) a class effect
    • McAlister F., Laupacis A., Wells G., and Sackett D. Users' Guides to the Medical Literature: XIX. Applying clinical trial results B. Guidelines for determining whether a drug is exerting (more than) a class effect. JAMA 282 (1999) 1371-1377
    • (1999) JAMA , vol.282 , pp. 1371-1377
    • McAlister, F.1    Laupacis, A.2    Wells, G.3    Sackett, D.4
  • 39
    • 0029987569 scopus 로고    scopus 로고
    • Trials to assess equivalence: The importance of rigorous methods [published correction appears in BMJ. 1996;313:550]
    • Jones B., Jarvis P., Lewis J., and Ebbutt A. Trials to assess equivalence: The importance of rigorous methods [published correction appears in BMJ. 1996;313:550]. BMJ 313 (1996) 36-39
    • (1996) BMJ , vol.313 , pp. 36-39
    • Jones, B.1    Jarvis, P.2    Lewis, J.3    Ebbutt, A.4
  • 40
    • 34547564771 scopus 로고    scopus 로고
    • www.emea.eu.int/pdfs/human/ewp/048299en.pdf
  • 41
    • 0142122889 scopus 로고    scopus 로고
    • Study design in osteoporosis: A European perspective
    • Kanis J., Alexandre J., Bone H., et al. Study design in osteoporosis: A European perspective. J Bone Miner Res 18 (2003) 1133-1138
    • (2003) J Bone Miner Res , vol.18 , pp. 1133-1138
    • Kanis, J.1    Alexandre, J.2    Bone, H.3
  • 42
    • 33744737506 scopus 로고    scopus 로고
    • Multicenter, randomized, double-blind, active-controlled, parallel-group trial of the long-term (6-12 months) safety of acetaminophen in adult patients with osteoarthritis
    • Temple A., Benson G., Zinsenheim J., and Schweinle J. Multicenter, randomized, double-blind, active-controlled, parallel-group trial of the long-term (6-12 months) safety of acetaminophen in adult patients with osteoarthritis. Clin Ther 28 (2006) 222-235
    • (2006) Clin Ther , vol.28 , pp. 222-235
    • Temple, A.1    Benson, G.2    Zinsenheim, J.3    Schweinle, J.4
  • 43
    • 0037160968 scopus 로고    scopus 로고
    • Cardiovascular morbidity and mortality in the Losartan Intervention For Endpoint reduction in hypertension study (LIFE): A randomised trial against atenolol
    • for the LIFE Study Group
    • for the LIFE Study Group. Dahlof B., Devereux R., Kjeldsen S., et al. Cardiovascular morbidity and mortality in the Losartan Intervention For Endpoint reduction in hypertension study (LIFE): A randomised trial against atenolol. Lancet 359 (2002) 995-1003
    • (2002) Lancet , vol.359 , pp. 995-1003
    • Dahlof, B.1    Devereux, R.2    Kjeldsen, S.3
  • 44
    • 0036303922 scopus 로고    scopus 로고
    • Uncertain future of trials in osteoporosis
    • Kanis J., Oden A., Johnell O., et al. Uncertain future of trials in osteoporosis. Osteoporos Int 13 (2002) 443-449
    • (2002) Osteoporos Int , vol.13 , pp. 443-449
    • Kanis, J.1    Oden, A.2    Johnell, O.3
  • 45
    • 0142091176 scopus 로고    scopus 로고
    • Ethical issues in clinical research on fracture prevention in patients with osteoporosis
    • Fost N. Ethical issues in clinical research on fracture prevention in patients with osteoporosis. J Bone Miner Res 18 (2003) 1110-1115
    • (2003) J Bone Miner Res , vol.18 , pp. 1110-1115
    • Fost, N.1
  • 46
    • 0033039349 scopus 로고    scopus 로고
    • Larger increases in bone mineral density during alendronate therapy are associated with a lower risk of new vertebral fractures in women with postmenopausal osteoporosis
    • for the Fracture Intervention Trial Research Group
    • for the Fracture Intervention Trial Research Group. Hochberg M., Ross P., Black D., et al. Larger increases in bone mineral density during alendronate therapy are associated with a lower risk of new vertebral fractures in women with postmenopausal osteoporosis. Arthritis Rheum 42 (1999) 1246-1254
    • (1999) Arthritis Rheum , vol.42 , pp. 1246-1254
    • Hochberg, M.1    Ross, P.2    Black, D.3
  • 47
    • 2942739433 scopus 로고    scopus 로고
    • Relationship between changes in biochemical markers of bone turn-over and BMD to predict vertebral fracture risk
    • Sarkar S., Reginster J., Crans G., et al. Relationship between changes in biochemical markers of bone turn-over and BMD to predict vertebral fracture risk. J Bone Miner Res 19 (2004) 394-401
    • (2004) J Bone Miner Res , vol.19 , pp. 394-401
    • Sarkar, S.1    Reginster, J.2    Crans, G.3
  • 48
    • 0141625900 scopus 로고    scopus 로고
    • Relationship of early changes in bone resorption to the reduction in fracture risk with risedronate
    • Eastell R., Barton I., Hannon R., et al. Relationship of early changes in bone resorption to the reduction in fracture risk with risedronate. J Bone Miner Res 18 (2003) 1051-1056
    • (2003) J Bone Miner Res , vol.18 , pp. 1051-1056
    • Eastell, R.1    Barton, I.2    Hannon, R.3
  • 49
    • 13144306555 scopus 로고    scopus 로고
    • Change in bone turn-over and hip, non-spine, and vertebral fracture in alendronate-treated women: The Fracture Intervention Trial
    • for the Fracture Intervention Trial Study Group
    • for the Fracture Intervention Trial Study Group. Bauer D., Black D., Garnero P., et al. Change in bone turn-over and hip, non-spine, and vertebral fracture in alendronate-treated women: The Fracture Intervention Trial. J Bone Miner Res 19 (2004) 1250-1258
    • (2004) J Bone Miner Res , vol.19 , pp. 1250-1258
    • Bauer, D.1    Black, D.2    Garnero, P.3
  • 50
    • 0036284616 scopus 로고    scopus 로고
    • Changes in bone density and turnover explain the reductions in incidence of nonvertebral fractures that occur during treatment with antiresorptive agents
    • Hochberg M., Greenspan S., Wasnich R., et al. Changes in bone density and turnover explain the reductions in incidence of nonvertebral fractures that occur during treatment with antiresorptive agents. J Clin Endocrinol Metab 87 (2002) 1586-1592
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 1586-1592
    • Hochberg, M.1    Greenspan, S.2    Wasnich, R.3
  • 51
    • 0034456357 scopus 로고    scopus 로고
    • Antifracture efficacy of antiresorptive agents are related to changes in bone density
    • Wasnich R., and Miller P. Antifracture efficacy of antiresorptive agents are related to changes in bone density. J Clin Endocrinol Metab 85 (2000) 231-236
    • (2000) J Clin Endocrinol Metab , vol.85 , pp. 231-236
    • Wasnich, R.1    Miller, P.2
  • 52
    • 18744388892 scopus 로고    scopus 로고
    • How useful are measures of BMD and bone turnover?
    • Miller P., Hochberg M., Wehren L., et al. How useful are measures of BMD and bone turnover?. Curr Med Res Opin 21 (2005) 545-554
    • (2005) Curr Med Res Opin , vol.21 , pp. 545-554
    • Miller, P.1    Hochberg, M.2    Wehren, L.3
  • 53
    • 14644401066 scopus 로고    scopus 로고
    • The roles of bone mineral density, bone turnover, and other properties in reducing fracture risk during antiresorptive therapy
    • Epstein S. The roles of bone mineral density, bone turnover, and other properties in reducing fracture risk during antiresorptive therapy. Mayo Clin Proc 80 (2005) 379-388
    • (2005) Mayo Clin Proc , vol.80 , pp. 379-388
    • Epstein, S.1
  • 54
    • 0033581212 scopus 로고    scopus 로고
    • Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: Results from a 3-year randomized clinical trial [published correction appears in JAMA. 1999;282:2124]
    • for the Multiple Outcomes of Raloxifene Evaluation (MORE) Investigators
    • for the Multiple Outcomes of Raloxifene Evaluation (MORE) Investigators. Ettinger B., Black D., Mitlak B., et al. Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: Results from a 3-year randomized clinical trial [published correction appears in JAMA. 1999;282:2124]. JAMA 282 (1999) 637-645
    • (1999) JAMA , vol.282 , pp. 637-645
    • Ettinger, B.1    Black, D.2    Mitlak, B.3
  • 55
    • 0028851590 scopus 로고
    • Effect of oral alendronate on bone mineral density and the incidence of fractures in postmenopausal osteoporosis
    • for the Alendronate Phase III Osteoporosis Treatment Study Group
    • for the Alendronate Phase III Osteoporosis Treatment Study Group. Liberman U., Weiss S., Broll J., et al. Effect of oral alendronate on bone mineral density and the incidence of fractures in postmenopausal osteoporosis. N Engl J Med 333 (1995) 1437-1443
    • (1995) N Engl J Med , vol.333 , pp. 1437-1443
    • Liberman, U.1    Weiss, S.2    Broll, J.3
  • 57
    • 33745034449 scopus 로고    scopus 로고
    • Intravenous ibandronate injections in postmenopausal women with osteoporosis: One-year results from the dosing intravenous administration study
    • Delmas P., Adami S., Strugala C., et al. Intravenous ibandronate injections in postmenopausal women with osteoporosis: One-year results from the dosing intravenous administration study. Arthritis Rheum 54 (2006) 1838-1846
    • (2006) Arthritis Rheum , vol.54 , pp. 1838-1846
    • Delmas, P.1    Adami, S.2    Strugala, C.3
  • 58
    • 85058905933 scopus 로고    scopus 로고
    • Rationale and design of the MOTION study (Monthly Oral Therapy with lbandronate for Osteoporosis iNtervention)
    • Cosman F., McClung M., Rosen C., et al. Rationale and design of the MOTION study (Monthly Oral Therapy with lbandronate for Osteoporosis iNtervention). J Bone Miner Res 20 Suppl 1 (2005) S398
    • (2005) J Bone Miner Res , vol.20 , Issue.SUPPL. 1
    • Cosman, F.1    McClung, M.2    Rosen, C.3
  • 59
    • 10744232538 scopus 로고    scopus 로고
    • Comparison of change in bone resorption and bone mineral density with once-weekly alendronate and daily risedronate: A randomised, placebo-controlled study
    • Hosking D., Adami S., Felsenberg D., et al. Comparison of change in bone resorption and bone mineral density with once-weekly alendronate and daily risedronate: A randomised, placebo-controlled study. Curr Med Res Opin 19 (2003) 383-394
    • (2003) Curr Med Res Opin , vol.19 , pp. 383-394
    • Hosking, D.1    Adami, S.2    Felsenberg, D.3
  • 60
    • 14644407147 scopus 로고    scopus 로고
    • Treatment with once-weekly alendronate 70 mg compared with once-weekly risedronate 35 mg in women with postmenopausal osteoporosis: A randomized double-blind study
    • for the Fosamax Actonel Comparison Trial Investigators
    • for the Fosamax Actonel Comparison Trial Investigators. Rosen C., Hochberg M., Bonnick S., et al. Treatment with once-weekly alendronate 70 mg compared with once-weekly risedronate 35 mg in women with postmenopausal osteoporosis: A randomized double-blind study. J Bone Miner Res 20 (2005) 141-151
    • (2005) J Bone Miner Res , vol.20 , pp. 141-151
    • Rosen, C.1    Hochberg, M.2    Bonnick, S.3
  • 61
    • 34547564310 scopus 로고    scopus 로고
    • www.clinicaltrials.gov/ct/show/nct00247273?order=1
  • 62
    • 33745773090 scopus 로고    scopus 로고
    • Comparison of weekly treatment of postmenopausal osteoporosis with alendronate versus risedronate over two years
    • Bonnick S., Saag K., Kiel D., et al. Comparison of weekly treatment of postmenopausal osteoporosis with alendronate versus risedronate over two years. J Clin Endocrinol Metab. 91 (2006) 2631-2637
    • (2006) J Clin Endocrinol Metab. , vol.91 , pp. 2631-2637
    • Bonnick, S.1    Saag, K.2    Kiel, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.