阿斯利康乳腺癌候选药物未获FDA咨询委员会投票通过

环球市场播报05-01

在乳腺癌候选药物未能在一项关键的咨询委员会投票中获得支持后，英国制药集团阿斯利康（AstraZeneca）表示，该公司将继续与美国监管机构合作，对该药物进行审查。　　这家制药商是英国富时100指数成分股。该公司周四晚间表示，美国食品药品管理局（Food and Drug Administration，简称FDA）的肿瘤药物咨询委员会以6比3的投票结果，对乳腺癌治疗候选药物...

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candidate not voted on by FDA advisory committee","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"AZN":1.5,"AZNH":1.1,"AZN.UK":1.5},"content_text":"在乳腺癌候选药物未能在一项关键的咨询委员会投票中获得支持后，英国制药集团阿斯利康（AstraZeneca）表示，该公司将继续与美国监管机构合作，对该药物进行审查。\n　　这家制药商是英国富时100指数成分股。该公司周四晚间表示，美国食品药品管理局（Food and Drug Administration， 简称FDA）的肿瘤药物咨询委员会以6比3的投票结果，对乳腺癌治疗候选药物camizestrant的获益-风险评估给出否定性意见。\n　　该公司表示：“在FDA完成对该申请的审查之际，阿斯利康将继续与其合作。”该监管机构不受该咨询委员会指导意见的约束，但会考虑其建议。\n　　阿斯利康的苏珊．加尔布雷思（Susan Galbraith）表示：“我们坚信Serena-6试验（测试camizestrant）的结果，也很高兴该委员会将camizestrant视为一种安全有效的潜在新药。”\n　　花旗（Citi）分析师写道，该委员会会议上出现了一些对该药物未来发展有利的积极迹象。\n　　花旗表示：“对于正在进行的更大规模试验而言，重要的是，投反对票的委员似乎并未对药物毒性抱有重大担忧。”\n　　该制药商本周早些时候表示，抗癌药物是今年第一季度收入增长的核心，肿瘤业务较上年同期实现了两位数增长。近年来，阿斯利康一直押注其肿瘤业务来刺激增长，将新药推向市场，并努力扩大现有药物的适应症范围。肿瘤业务目前占集团收入的近一半。\n　　Jefferies的分析师表示，camizestrant审批受挫对该股而言并不是一个严重问题。\n　　该行在给投资者的一份报告中表示：“除了可能对市场情绪造成打击外，这不应该是一个重大问题，任何走弱都提供了买入机会。”阿斯利康的股价在周五开盘交易中下跌了约1.8%。\n\n\n海量资讯、精准解读，尽在新浪财经APP\n\n责任编辑：刘明亮","kind":"news","is_publish_news":true,"is_publish_highlight":false,"is_publish_live":false,"is_publish_wemedia":null,"editions":null,"column":"","sentiment":"-1","news_tag":"productRelease","news_rank":0,"isVideo":false,"video":null,"symbols":[],"gpt_button":1,"need_auth":false,"need_login_tip":false,"code":"91000000","status":"200"},"commentList":[],"isCommentEnd":true,"newsSizeData":{"likeSize":0,"commentSize":0,"repostSize":0,"favoriteSize":0,"likeStatus":false,"favoriteStatus":false},"APP":{"userAgent":"Mozilla/5.0 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