A Study of Quarterly Intravenous Bonviva (Ibandronate) in Women With Post-Menopausal Osteoporosis.
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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.
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Ages Eligible for Study:
up to 80 Years (Child, Adult, Older Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
post-menopausal women with osteoporosis;
<=80 years of age;
naive to oral bisphosphonates, or have discontinued daily and/or weekly bisphosphonate treatment for >1 year.
metabolic bone disease other than post-menopausal osteoporosis;
treatment with other drugs affecting bone metabolism within last 6 months;
previous or current malignant disease (except for adequately treated cancer in situ of the cervix, or basal or squamous cell skin cancer).