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信达生物

79.950

+6.8009.30%

成交量：2,537.27万

成交额：19.57亿

市值：1,320.77亿

市盈率：-1,259.04

高：80.050

开：74.550

低：72.900

收：73.150

数据加载中...

总览公司新闻公告

信达生物下跌2.76%，报72.2元/股

信达生物盘中异动快速跳水3.03%

券商观点|创新药行业专题研究报告：创新突破，出海拓疆

再获BTD：信达生物IBI363（PD-1/IL-2α-bias双特异性抗体融合蛋白）获国家药品监督管理局纳入突破性治疗药物品种，治疗免疫耐药鳞状非小细胞肺癌

和黄医药(00013)与信达生物(01801)宣布：呋喹替尼联合信迪利单抗用于治疗晚期肾细胞癌的中国新药上市申请获受理

信达生物抗CLDN18.2 ADC新药I期数据惊艳，剑指癌王 | 2025 ASCO

资金动向 | 北水加仓美团超14亿港元，减仓腾讯、小米

每日卖空追踪 | 信达生物 06月04日卖空量成交534.85万股，卖空比例为8.78%

港股收盘，恒指收涨0.6%，科指收涨0.57%。大市多数板块收涨，大消费、医药板块表现强势，泡泡玛特(09992.HK)

再传重磅利好！港股医药板块集体沸腾，机构研判后市布局主线

港股收评：恒生指数涨0.72% 稳定币概念股爆发

《股市简讯》恒生创新药指数飙近6%，券商称中国创新药产业有望持续高景气

恒生医药持续突破，年内涨幅超44%

每日经济新闻

信达生物上涨10.91%，报72.15元/股

港股异动 | 信达生物(01801)暴涨逾12% IBI363治疗晚期非小细胞肺癌临床PoC研究数据公布

国金证券：肿瘤创新药市场规模持续增长看好国内药企在乳腺癌领域的突破

中证香港100医药卫生指数报839.10点，前十大权重包含信达生物等

《大行》摩通：信达生物(01801.HK)IBI363及IBI343研究数据令人鼓舞目标价上调至74元

阿斯达克财经

信达生物盘中异动股价大涨3.01%报65.000港元

ASCO口头报告信达生物公布IBI343（创新型抗CLDN18.2 ADC）治疗晚期胰腺癌的I期临床研究数据更新

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08:30","pubTimestamp":1749083414,"startTime":"0","endTime":"0","summary":"2025年6月5日，东吴证券发布了一篇医药生物行业的研究报告，报告指出，创新突破，出海拓疆。其一创新药重磅BD有序落地，首付款屡创新高。创新药产业空间巨大，市场规模迎来快速爆发之势。中国创新药研发实力显著提升，原研FIC创新药取得突破。中国创新药授权出海爆发，BD数量与金额再创新高。2025ASCO会议共有来自中国的73项口头报告，数量创下历史新高。中国企业发布双抗研究约34项，占整体双抗研究的比例约49%。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250605083444a6fae8f5&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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08:23","pubTimestamp":1749082980,"startTime":"0","endTime":"0","summary":"截至目前，IBI363在鳞状非小细胞肺癌和黑色素瘤的两项适应症已经分别获得中国CDE的BTD认证和美国FDA快速通道资格认定，此次BTD标志着IBI363在解决免疫耐药及冷肿瘤治疗难题中再前进一步。IBI363在既往接受过免疫治疗的鳞状非小细胞肺癌受试者的临床I期研究最新数据在2025年ASCO大会上以 口头形式报告 。在今年ASCO会议上，IBI363口头报告了在免疫耐药非小细胞肺癌、结直肠癌、黑色素瘤三项免疫耐药及冷肿瘤中的突破性临床研究结果，并获得广泛关注。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://wwwold.prnasia.com/story/archive/4703001_ZH03001_1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"prnasia","symbols":["LU1969619763.USD","LU1169589451.USD","01801","BK1583","LU2328871848.SGD","PD","LU1169590202.USD","LU2488822045.USD","BK1589","BK4023","BK1161"],"gpt_icon":0},{"id":"2541097206","title":"和黄医药(00013)与信达生物(01801)宣布：呋喹替尼联合信迪利单抗用于治疗晚期肾细胞癌的中国新药上市申请获受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2541097206","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2541097206?lang=zh_cn&edition=fundamental","pubTime":"2025-06-05 07:55","pubTimestamp":1749081356,"startTime":"0","endTime":"0","summary":"智通财经APP讯，和黄医药 与信达生物联合宣布，呋喹替尼 和信迪利单抗 联合疗法用于治疗既往接受过一种酪氨酸激酶抑制剂治疗失败的局部晚期或转移性的肾细胞癌患者的新药上市申请已获中国国家药品监督管理局受理。FRUSICA-2是一项随机、开放标签、阳性对照的注册研究，旨在评估呋喹替尼和信迪利单抗联合疗法对比阿昔替尼或依维莫司单药疗法用于二线治疗晚期肾细胞癌的疗效和安全性。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1301450.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1587","BK1588","BK4007","00013","BK4588","HCM","BK4531","BK1589","LU1969619763.USD","BK1161","LU2328871848.SGD","BK1191","LU2488822045.USD","BK4585","01801","BK1583"],"gpt_icon":0},{"id":"2541976070","title":"信达生物抗CLDN18.2 ADC新药I期数据惊艳，剑指癌王 | 2025 ASCO","url":"https://stock-news.laohu8.com/highlight/detail?id=2541976070","media":"药渡","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2541976070?lang=zh_cn&edition=fundamental","pubTime":"2025-06-05 07:32","pubTimestamp":1749079948,"startTime":"0","endTime":"0","summary":"根据GLOBOCAN 2022年的数据，2022年全球胰腺癌新发病例为51万，死亡病例为46.7万。它通过与表达CLDN18.2的肿瘤细胞结合，发生CLDN18.2依赖性ADC内化，并释放毒素药物引起DNA损伤，导致肿瘤细胞凋亡。研究的目的是评估IBI343在CLDN18.2表达阳性的晚期胰腺癌患者中的安全性、耐受性、药代动力学特征以及初步疗效。信达生物新闻稿中表示，IBI343是全球首个在晚期胰腺癌治疗中表现出良好疗效和安全性的ADC药物。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250605073556a6fada13&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, 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