The U.S. FDA Approves Novartis’ Kisqali® to Reduce the Risk of Recurrence in People with HR+/HER2- Early Breast Cancer

Novartis FDA Approval
Yesterday, September 17, 2024, Novartis (NVS) announced that the United States FDA has approved Kisqali®(ribociclib) in combination with an aromatase inhibitor (AI) for adjuvant treatment of people with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) stage II and III early breast cancer (EBC) at high risk of recurrence, including those . . .

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