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DOI 10.1359/jbmr.050313

Медицинская библиотека · Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2005

Monthly oral ibandronate therapy in postmenopausal osteoporosis: 1-year results from the MOBILE study.

Miller Paul D, McClung Michael R, Macovei Liviu, Stakkestad Jacob A, Luckey Marjorie, Bonvoisin Bernard, Reginster Jean-Yves, Recker Robert R, Hughes Claire, Lewiecki E Michael, Felsenberg Dieter, Delmas Pierre D, Kendler David L, Bolognese Michael A, Mairon Nicole, Cooper Cyrus

Клиническое исследованиеКлиническое исследование III фазыСтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: Once-monthly (50/50, 100, and 150 mg) and daily (2.5 mg; 3-year vertebral fracture risk reduction: 52%) oral ibandronate regimens were compared in 1609 women with postmenopausal osteoporosis. At least equivalent efficacy and similar safety and tolerability were shown after 1 year.

INTRODUCTION

Suboptimal adherence to daily and weekly oral bisphosphonates can potentially compromise therapeutic outcomes in postmenopausal osteoporosis. Although yet to be prospectively shown in osteoporosis, evidence from randomized clinical trials in several other chronic conditions shows that reducing dosing frequency enhances therapeutic adherence. Ibandronate is a new and potent bisphosphonate with antifracture efficacy proven for daily administration and also intermittent administration with a dose-free interval of >2 months. This report presents comparative data on the efficacy and safety of monthly and daily oral ibandronate regimens.

MATERIALS AND

METHODS

MOBILE is a 2-year, randomized, double-blind, phase III, noninferiority trial. A total of 1609 women with postmenopausal osteoporosis were assigned to one of four oral ibandronate regimens: 2.5 mg daily, 50 mg/50 mg monthly (single doses, consecutive days), 100 mg monthly, or 150 mg monthly.

RESULTS

After 1 year, lumbar spine BMD increased by 3.9%, 4.3%, 4.1%, and 4.9% in the 2.5, 50 /50, 100, and 150 mg arms, respectively. All monthly regimens were proven noninferior, and the 150 mg regimen superior, to the daily regimen. All monthly regimens produced similar hip BMD gains, which were larger than those with the daily regimen. All regimens similarly decreased serum levels of C-telopeptide, a biochemical marker of bone resorption. Compared with the daily regimen, a significantly larger proportion of women receiving the 100 and 150 mg monthly regimens achieved predefined threshold levels for percent change from baseline in lumbar spine (6%) or total hip BMD (3%). All regimens were similarly well tolerated.

CONCLUSIONS

Monthly ibandronate is at least as effective and well tolerated as the currently approved daily ibandronate regimen in postmenopausal osteoporosis.

Для цитирования: Miller Paul D, McClung Michael R, Macovei Liviu, Stakkestad Jacob A, Luckey Marjorie, Bonvoisin Bernard, Reginster Jean-Yves, Recker Robert R, Hughes Claire, Lewiecki E Michael, Felsenberg Dieter, Delmas Pierre D, Kendler David L, Bolognese Michael A, Mairon Nicole, Cooper Cyrus. Monthly oral ibandronate therapy in postmenopausal osteoporosis: 1-year results from the MOBILE study.. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 2005. DOI: 10.1359/jbmr.050313.

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