Abstract
Ibandronate is an aminobisphosphonate that targets bone and inhibits osteoclasts. It is one of the most potent bisphosphonates currently under clinical investigation in metabolic bone disease and osteoporosis. In animal models ibandronate is 2, 10, 50 and 500 times more potent than risedronate, alendronate, pamidronate, and clodronate, respectively, without any impairment of mineralization. Subcutaneous administration is as effective as intravenous administration, oral activity is 100 times lower. Tumor-related bone destruction of either humoral or metastatic origin is dramatically decreased. Bone loss and reduction in bone strength due to cessation of ovarian function is prevented by > 1 μg/kg/day subcutaneously. The total dose rather than the treatment schedule seems to be important for efficacy. Studies on bone quality following long-term treatment demonstrated normal bone without any signs of deterioration.