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ADVISORY...for FRIDAY (Feb. 22)
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--(BUSINESS WIRE)
The U.S. Food and Drug Administration (FDA) today approved the Novartis drug ZOMETA(R) (zoledronic acid for injection) for the treatment of patients with multiple myeloma and patients with documented bone metastases from solid tumors, in conjunction with standard antineoplastic therapy.
These solid tumors include prostate cancer, lung cancer, breast cancer and other solid tumor types. In prostate cancer, patients should have progressed after treatment with at least one hormonal therapy.
The trials that led to the approval of ZOMETA mark the first time any bisphosphonate has demonstrated efficacy in treating bone complications in patients with prostate cancer, lung cancer and other solid tumors.
Further, ZOMETA offers patients, nurses and clinicians a convenient 4 mg, 15-minute infusion time.
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