Wednesday, April 19, 2006

New drug Bondronat vs. Zometa

New Data Support Bondronat's Superior Renal Safety Profile Against Zometa

New data announced at the 8th workshop on bisphosphonates in Davos shows Roche's Bondronat® (ibandronate) is associated with significantly less kidney damage than another commonly used bisphosphonate, zoledronic acid (Zometa), in multiple myeloma patients with bone lesions.

Although Bondronat is not currently licensed for use in multiple myeloma, the audit results add to evidence from previous studies which indicate that Bondronat has renal safety similar to placebo, unlike other bisphosphonates.

Multiple myeloma is a cancer of the blood which develops in the bone marrow of patients. Bisphosphonates are used to treat the bone lesions that result from the cancer -- these lesions give rise to a high risk of fractures and considerable bone pain. Approximately 50% of multiple myeloma patients experience kidney problems, making renal safety a key consideration for physicians.

In the audit, rates of renal impairment over a 4 year period were reviewed retrospectively in records of multiple myeloma patients treated with either Bondronat or zoledronic acid. The results showed:

· Patients taking Bondronat were three times less likely to suffer renal impairment than those taking zoledronic acid: 10.8% for Bondronat vs. 39.1% with zoledronic acid (based on serum creatinine levels).

· The incidence rate of renal impairment was significantly higher in patients taking zoledronic acid: 0.87 events with Bondronat versus 2.65 events with zoledronic acid per person-year (indicated by the glomerular filtration rate, a recognized measure of renal function).

"These data confirm findings from previous studies and again highlight Bondronat's renal safety advantages over other bisphosphonates. They are especially promising given the particular risk of kidney complications faced by multiple myeloma patients," said Dr. Raoul Bergner from the Klinikum der Stadt Ludwigshafen in
Ludwigshafen, Germany. "Patients with multiple myeloma experiencing bone pain may benefit from the loading dose currently under investigation in an international phase III study in cancer patients with bone metastases. The good renal safety profile means Bondronat can be given on 3 consecutive days without causing kidney damage."

In a further two studies also presented today, Bondronat was found to be suitable for use in patients with relapsed or refractory multiple myeloma and well-tolerated in multiple myeloma patients who had reached end stage renal disease, requiring haemodialysis. These promising results are being further evaluated in two multi-centre, multi-national phase III trials in multiple myeloma patients, investigating the efficacy and renal safety of Bondronat in these patients.

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