An expanded access record providing ibandronate [Bonviva/Boniva] in Postmenopausal Osteoporosis, sponsored by Hoffmann-La Roche. No longer available at 14 sites in Taiwan. Open to female participants aged Up to 80 Years. Per ClinicalTrials.gov, last updated 2016-11-02.
Sponsored by Hoffmann-La Roche · Expanded access
This single arm study will assess the efficacy and safety of quarterly intravenous Bonviva in women with post-menopausal osteoporosis. All patients will receive Bonviva 3mg i.v. every 3 months. The anticipated time on study treatment is 3-12 months, and the target sample size is 100 individuals.
1,640 studies on the registry are indexed under Osteoporosis; 212 are open to participants now.
Browse Osteoporosis studies →Hoffmann-La Roche is the lead sponsor of 2,061 studies on the registry; 85 are open to participants now.
Of its 319 completed or terminated interventional studies of FDA-regulated products, 239 (75%) have results posted.
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3mg iv every 3 months
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Hoffmann-La Roche