FDA Approves Novartis Kisqali To Reduce Risk Of Recurrence In People With HR+/HER2- Early Breast Cancer
Portfolio Pulse from Benzinga Newsdesk
The FDA has approved Novartis' drug Kisqali for reducing the risk of recurrence in patients with HR+/HER2- early breast cancer. This approval could potentially boost Novartis' market position in the oncology sector.
September 17, 2024 | 5:05 pm
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Novartis received FDA approval for its drug Kisqali, aimed at reducing recurrence risk in HR+/HER2- early breast cancer patients. This approval could enhance Novartis' competitive edge in the oncology market.
The FDA approval of Kisqali is a significant regulatory milestone for Novartis, likely to positively impact its stock price due to the potential increase in market share and revenue in the oncology sector.
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