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泰格醫藥

26.550

-0.200-0.75%

成交量：96.74萬

成交額：2,567.27萬

市值：229.64億

市盈率：53.10

高：26.950

開：26.550

低：26.150

收：26.750

資料載入中...

總覽公司新聞公告

【石藥集團(01093.HK)：JMT203(抗GFRAL單克隆抗體)獲美國臨牀試驗批准】石藥集團(01093.HK)發佈公告，公司附屬公司上海津曼特生物科技有限公司自主研發的抗體藥物JMT203已獲美國食品藥品監督管理局(FDA)批准，可以在美國開展臨牀研究。此前，該產品已經於2023年6月獲得中國國家藥品監督管理局批准，並正在中國開展臨牀試驗。

石藥集團(01093)：JMT203(抗GFRAL單克隆抗體)獲美國臨牀試驗批准

科倫博泰生物-B現漲超4% 創新ADC藥物SKB518新藥臨牀試驗申請獲FDA批准

醫藥外包概念全線飄紅藥明生物(02269)漲超3% 機構指板塊存在超跌機會 FDA新政下AI製藥價值凸顯

中歐基金葛蘭：看好創新藥、消費醫療、醫療設備等板塊投資機遇

港股異動 | 先聲藥業(02096)現漲超8% SIM0686獲準開展臨牀試驗後續多款新藥獲批在望

奧辰生物（雲南）有限公司藥品申請臨牀試驗默示許可獲受理

吉利德科學(GILD.O)宣佈Trodelvy（戈沙妥珠單抗）聯合Keytruda（帕博利珠單抗）在第三級臨牀試驗中達到

科倫藥業：子公司SKB518新藥臨牀試驗申請獲FDA批准

科倫博泰生物-B(06990)：創新ADC藥物SKB518新藥臨牀試驗申請獲美國食品藥品監督管理局批准

恆瑞醫藥：子公司收到藥物臨牀試驗批准通知書

【百奧泰：注射用BAT7111獲藥物臨牀試驗批准】百奧泰公告，公司於近日收到國家藥監局覈准簽發的《藥物臨牀試驗批准通知書》，公司在研藥品注射用BAT7111用於晚期實體瘤的臨牀試驗申請獲得批准。根據《Clinical Development Success Rates2011-2020》公佈的數據，通常情況下對於抗腫瘤藥物，一般I/II期臨牀研究階段持續約2年時間，I期完成進入II期的比率約48.8%，II期完成進入III期的比率約24.6%。考慮到臨牀研究週期長、投入大，過程中不可預測因素較多，臨牀試驗、審評和審批的結果以及時間都具有一定的不確定性。

中國人民銀行等四部門：加大對出口企業的保險支持力度

晚期實體瘤藥物喜訊不斷，人福醫藥、匯宇製藥、翰森製藥等多藥企獲批臨牀試驗

【改善患者肢體運動功能 “植入式迷走神經刺激系統”臨牀試驗啓動】今天，國家衞生健康委組織實施的“百萬減殘”工程重點推廣項目，我國自主研發的“植入式迷走神經刺激系統”臨牀試驗正式全國啓動。該項目有望成為我國卒中後殘疾防控的重要手段。

Sands Capital Management,LP減持泰格醫藥(03347)38.41萬股每股作價為25.9329港元

【沃森生物：20價肺炎球菌多糖結合疫苗獲臨牀試驗批准】沃森生物公告，公司及子公司共同申請的20價肺炎球菌多糖結合疫苗獲得國家藥品監督管理局簽發的《藥物臨牀試驗批准通知書》，通知書編號為2025LP01099。該疫苗是在已上市產品13價肺炎球菌多糖結合疫苗基礎上開發的迭代升級產品，新增了8型、10A型、11A型、12F型、15B型、22F型和33F型共計7種血清型，用於預防由本品所含20種肺炎球菌血清型引起的感染性疾病。全球已上市20價肺炎球菌多糖結合疫苗的廠家僅有美國輝瑞公司一家，國內尚未有20價肺炎球菌多糖結合疫苗上市銷售。

盛禾（中國）生物製藥有限公司藥品申請臨牀試驗默示許可獲受理

石藥集團歐意藥業有限公司藥品申請臨牀試驗默示許可獲受理

普方生物製藥（蘇州）有限公司藥品申請臨牀試驗默示許可獲受理

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涨3.17%，凯莱英涨2.55%，昭衍新药涨2.55%，康龙化成涨1.78%，药明康德涨1.73%，金斯瑞生物科技涨1.54%，泰格医药涨1.56%。交银国际研报指，中美多次调整关税政策。FDA称此举旨在加速评估流程，减少动物实验，降低研发成本并最终降低药品价格。该行指，FDA宣布取消动物实验长期有望利好AI制药企业。该行认为市场对于关税对医药板块的影响存在过度担忧，仍存在超跌情况。","market":"sg","thumbnail":"https://static.szfiu.com/news/20210810/ZTUyNTQ0NjcxODUwNQ==.jpg","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20210810/ZTUyNTQ0NjcxODUwNQ==.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"1957468","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1141","LU2242644610.SGD","LU2039709279.SGD","IE00B0JY6N72.USD","LU0052750758.USD","LU0823426480.USD","LU1242518857.USD","LU0359202008.SGD","01548","09939","LU0181495838.USD","LU1794554557.SGD","LU0516423091.SGD","LU0572944931.SGD","LU0043850808.USD","BK1576","02269","159938","LU2125910500.SGD","SG9999002562.SGD","03759","LU0307460666.USD","02359","LU0588546209.SGD","HK0000320264.USD","LU1242518931.SGD","LU0348825331.USD","LU0348735423.USD","LU0456846285.SGD","HK0000306701.USD","LU0327786744.USD","LU0417516738.SGD","01477","LU0516422440.USD","HK0000306685.HKD","BK1589","06127","LU0823426308.USD","03347","06821","LU0708995583.HKD","LU0320764599.SGD","LU0516422952.EUR","LU0417516902.SGD","LU1720050803.USD","LU1688375341.USD","LU0856984785.SGD","LU2045819591.USD","LU0359201612.USD","BK1574"],"gpt_icon":0},{"id":"2529336012","title":"中歐基金葛蘭：看好創新藥、消費醫療、醫療設備等板塊投資機遇","url":"https://stock-news.laohu8.com/highlight/detail?id=2529336012","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529336012?lang=zh_tw&edition=fundamental","pubTime":"2025-04-22 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批准SKB518用于晚期实体瘤的IND申请的临床试验通知书。SKB518的1期临床试验正在中国进行中。","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/1281560.html","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":"stock_zhitongcaijing","symbols":["BK1141","BK4080","BK1576","ADC","BK4231","06990","BK1161","LU0196878994.USD","BK1583","03347"],"gpt_icon":0},{"id":"2529824524","title":"恆瑞醫藥：子公司收到藥物臨牀試驗批准通知書","url":"https://stock-news.laohu8.com/highlight/detail?id=2529824524","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529824524?lang=zh_tw&edition=fundamental","pubTime":"2025-04-21 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Development Success Rates2011-2020》公佈的數據，通常情況下對於抗腫瘤藥物，一般I/II期臨牀研究階段持續約2年時間，I期完成進入II期的比率約48.8%，II期完成進入III期的比率約24.6%。考慮到臨牀研究週期長、投入大，過程中不可預測因素較多，臨牀試驗、審評和審批的結果以及時間都具有一定的不確定性。","url":"https://stock-news.laohu8.com/highlight/detail?id=2529288268","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529288268?lang=zh_tw&edition=fundamental","pubTime":"2025-04-21 15:42","pubTimestamp":1745221338,"startTime":"0","endTime":"0","summary":"百奥泰公告，公司于近日收到国家药监局核准签发的《药物临床试验批准通知书》，公司在研药品注射用BAT7111用于晚期实体瘤的临床试验申请获得批准。根据《Clinical Development Success 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