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FDA advisory panel votes against Daiichi Sankyo's blood cancer treatment [Reuters (UK)]

DAIICHI SANKYO S/ADR (DSNKY) 
Company Research Source: Reuters
FDA advisory panel votes against Daiichi Sankyo's blood cancer treatment - Reuters 2 Min Read (Reuters) - Independent experts on an advisory panel to the U.S. Food and Drug Administration on Tuesday voted against Daiichi Sankyo Co Ltd’s treatment for adults with a type of acute myeloid leukemia. The panel voted 8-3 against the drug, quizartinib, after assessing data presented by the Japanese company. Separately, an advisory committee voted 12-3 in favor of the approval of pexidartinib, another treatment from Daiichi, that aims to treat a type of rare, non-cancerous tumor usually affecting joints and limbs. Daiichi has been focusing on oncology, targeting 500 billion yen ($4.52 billion) in annual sales from the business in fiscal 2025 from 20 billion yen in 2017. Quizartinib is aimed at treating acute myeloid leukemia patients with a specific genetic mutation called FLT3. While several members of the panel acknowledged the drug did appear to bridge patients toward a transplant, which c Show less Read more
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