4.5 Article

Efficacy of monthly oral ibandronate is sustained over 5 years: the MOBILE long-term extension study

Journal

OSTEOPOROSIS INTERNATIONAL
Volume 23, Issue 6, Pages 1747-1756

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s00198-011-1773-0

Keywords

Bisphosphonate; Clinical study; Ibandronate; Long-term treatment; Postmenopausal osteoporosis

Funding

  1. F. Hoffmann-La Roche
  2. GlaxoSmithKline
  3. Merck
  4. Lilly
  5. Wyeth
  6. Procter and Gamble
  7. Amgen
  8. Roche
  9. Novartis
  10. NPS Allelix
  11. Sanofi-Aventis
  12. Servier
  13. Negma
  14. Merckle
  15. Nycomed
  16. NPS
  17. Theramex
  18. UCB
  19. Bristol Myers Squibb
  20. Merck Sharp Dohme
  21. Rottapharm
  22. Teva
  23. Warner Chillcott
  24. Genentech
  25. Eli Lilly
  26. Merck Co.
  27. Novartis Pharmaceuticals

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The long-term efficacy and safety of once-monthly ibandronate were studied in this extension to the 2-year Monthly Oral Ibandronate in Ladies (MOBILE) trial. Over 5 years, lumbar spine bone mineral density (BMD) increased from baseline with monthly ibandronate 150 mg (8.4%). Long-term monthly ibandronate is effective and well tolerated for up to 5 years in women with postmenopausal osteoporosis. Once-monthly therapy with ibandronate has been studied for up to 5 years in a long-term extension (LTE) to the 2 year MOBILE trial. This multicenter, double-blind extension study of monthly ibandronate involved postmenopausal women who had completed 2 years of the MOBILE core study, with a parts per thousand yen75% adherence. Patients were reallocated, or were randomized from daily therapy, to ibandronate 100 mg monthly or 150 mg monthly for a further 3 years. A pooled intent-to-treat (ITT) analysis of 344 patients receiving monthly ibandronate from the core MOBILE baseline showed increases over 5 years in lumbar spine BMD (8.2% with 100 mg and 8.4% with 150 mg). Three-year data relative to MOBILE LTE baseline in the full ITT population of all 698 patients randomized or reallocated from MOBILE (including those previously on daily treatment) showed, on average, maintenance of proximal femur BMD gains achieved in the core 2-year study, with further small gains in lumbar spine BMD. In general, maintenance of efficacy was also indicated by markers of bone metabolism. There were no tolerability concerns or new safety signals. Monthly treatment with ibandronate 100 and 150 mg is effective and well tolerated for up to 5 years in women with postmenopausal osteoporosis.

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