港股詳情

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泰格醫藥

27.200

+0.4501.68%

成交量：73.46萬

成交額：1,925.60萬

市值：235.27億

市盈率：53.91

高：27.250

開：26.600

低：25.400

收：26.750

資料載入中...

總覽公司新聞公告

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

江蘇華益科技有限公司藥品申請臨牀試驗默示許可獲受理

兆科眼科-B(06622)：環孢素A眼凝膠新一輪第III期臨牀試驗入組首名患者

南京維立志博生物科技股份有限公司藥品申請臨牀試驗默示許可獲受理

信達生物醫藥科技（杭州）有限公司藥品申請臨牀試驗默示許可獲受理

江西銀濤藥業股份有限公司藥品申請臨牀試驗默示許可獲受理

武漢人福創新藥物研發中心有限公司藥品申請臨牀試驗默示許可獲受理

泰格醫藥收盤下跌2.37%，滾動市盈率93.04倍，總市值376.94億元

衞信康(603676.SH)子公司琥珀酰明膠電解質醋酸鈉注射液獲批臨牀試驗

翰森製藥（3692.HK）自主研發的靶向KRAS G12D小分子1類新藥HS-10529片獲NMPA簽發的藥物臨牀試驗批准通知書

泰格醫藥盤中異動急速下挫5.00%

【華泰證券：AI醫療產業趨勢正在加速】華泰證券研報表示，4月10日，美國FDA宣佈將通過一系列方法減少、改進或取代在單克隆抗體療法及其他藥物的研發中動物試驗要求，包括基於AI的毒性計算模型、在實驗室環境中進行的細胞系和類器官毒性測試。2025年計劃啓動試點項目，允許部分藥企在FDA監督下完全跳過動物實驗，全面政策更新預計2026年完成。FDA此項政策將進一步推動AI在新藥研發中的覆蓋，從化學合成環節加速走向臨牀前及臨牀試驗等生物環節，推動創新藥企業加大AI藥物發現平臺投入。再次強調2025年“AI+醫療”將迎來跨越式發展，應重視相關投資機會。

映恩生物登陸港交所首日大漲116.70%；百利天恆第10款ADC獲批臨牀試驗 | 醫藥早參

每日经济新闻

【翰森製藥HS-10529獲批臨牀，擬治療KRAS G12D突變晚期實體瘤】 4月15日，翰森製藥宣佈，公司自主研發的1類新藥HS-10529片獲國家藥品監督管理局簽發的藥物臨牀試驗批准通知書，擬開發治療KRAS G12D突變的晚期實體瘤。

翰森製藥(03692.HK)HS-10529片藥物臨牀試驗獲批

阿斯达克财经

翰森製藥(03692)：HS-10529片獲國家藥品監督管理局簽發的藥物臨牀試驗批准通知書

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13:40","pubTimestamp":1744954838,"startTime":"0","endTime":"0","summary":"4月18日，据CDE官网消息，石药集团欧意药业有限公司联合申请药品“普卢格列汀二甲双胍缓释片（Ⅰ）”，获得临床试验默示许可，受理号CXHL2500185。通过天眼查大数据分析，石药集团欧意药业有限公司共对外投资了11家企业，参与招投标项目5000次，知识产权方面有商标信息198条，专利信息197条，此外企业还拥有行政许可746个。主要股东信息显示，石药集团欧意药业有限公司由石药集团恩必普药业有限公司持股100%。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/18134049650524.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["LU0067412154.USD","IE00BZ08YS42.EUR","LU0326950275.SGD","IE00BZ08YT58.USD","BK1141","BK1521","LU1226287529.USD","LU0880133367.SGD","IE00B5MMRT66.SGD","LU1951186391.HKD","LU1807302812.USD","BK1191","01093","IE0008369823.USD","BK1576","03347","LU1152091754.HKD","LU1152091168.USD","SG9999004220.SGD","LU1008478684.HKD","LU0501845795.SGD","LU0072913022.USD","IE00B031HY20.USD","LU0140636845.USD","IE00BZ08YR35.GBP","LU1226287792.SGD","LU1226288170.HKD","LU1226288253.USD","IE0008368742.USD","LU1226287875.USD","BK1583","IE00B543WZ88.USD","LU1993786604.SGD","BK1515","LU1960683339.HKD"],"gpt_icon":0},{"id":"2528208778","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=2528208778","media":"金融界","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528208778?lang=zh_tw&edition=fundamental","pubTime":"2025-04-18 13:40","pubTimestamp":1744954838,"startTime":"0","endTime":"0","summary":"4月18日，据CDE官网消息，普方生物制药（苏州）有限公司联合申请药品“注射用GEN1184”，获得临床试验默示许可，受理号CXSB2500023。普方生物制药（苏州）有限公司，成立于2019年，位于苏州市，是一家以从事研究和试验发展为主的企业。主要股东信息显示，普方生物制药（苏州）有限公司由ProfoundBio Limited持股100%。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/18134049650527.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["BK1583","BK1141","BK1576","03347"],"gpt_icon":0},{"id":"2528087786","title":"江蘇華益科技有限公司藥品申請臨牀試驗默示許可獲受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2528087786","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528087786?lang=zh_tw&edition=fundamental","pubTime":"2025-04-18 13:40","pubTimestamp":1744954838,"startTime":"0","endTime":"0","summary":"4月18日，据CDE官网消息，江苏华益科技有限公司联合申请药品“铜[64Cu]氧奥曲肽注射液”，获得临床试验默示许可，受理号CYHL2500038。江苏华益科技有限公司，成立于2001年，位于苏州市，是一家以从事化学原料和化学制品制造业为主的企业。通过天眼查大数据分析，江苏华益科技有限公司共对外投资了20家企业，参与招投标项目74次，知识产权方面有商标信息10条，专利信息110条，此外企业还拥有行政许可45个。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/18134049650525.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["03347","BK1583","BK1576","BK1141"],"gpt_icon":0},{"id":"2528767363","title":"兆科眼科-B(06622)：環孢素A眼凝膠新一輪第III期臨牀試驗入組首名患者","url":"https://stock-news.laohu8.com/highlight/detail?id=2528767363","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528767363?lang=zh_tw&edition=fundamental","pubTime":"2025-04-17 17:00","pubTimestamp":1744880445,"startTime":"0","endTime":"0","summary":"智通财经APP讯，兆科眼科-B 发布公告，环孢素A眼凝胶用于治疗中重度干眼症的第III期临床试验已于2025年4月3日入组首名患者。该第III期临床试验为一项关于环孢素A眼凝胶对中重度干眼症患者的疗效及安全性的多中心、随机、双盲及安慰剂对照研究。于2024年7月，公司取得环孢素A眼凝胶新一轮第III期临床试验的新药临床试验申请监管批文。通过每日一次用药及迅速起效，公司的环孢素A眼凝胶有望显著改善患者的用药依从性和生活质量。","market":"sh","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/1280106.html","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":"stock_zhitongcaijing","symbols":["BK4134","03347","BK1141","06622","BK1191","III","BK1574","BK1583","BK1587","BK1576"],"gpt_icon":0},{"id":"2528823737","title":"南京維立志博生物科技股份有限公司藥品申請臨牀試驗默示許可獲受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2528823737","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528823737?lang=zh_tw&edition=fundamental","pubTime":"2025-04-17 12:16","pubTimestamp":1744863388,"startTime":"0","endTime":"0","summary":"4月17日，据CDE官网消息，南京维立志博生物科技股份有限公司联合申请药品“注射用LBL-024”，获得临床试验默示许可，受理号CXSL2500112。南京维立志博生物科技股份有限公司，成立于2012年，位于南京市，是一家以从事专业技术服务业为主的企业。通过天眼查大数据分析，南京维立志博生物科技股份有限公司共对外投资了3家企业，参与招投标项目2次，知识产权方面有商标信息40条，专利信息23条，此外企业还拥有行政许可27个。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/17121649612041.shtml","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":"jinrongjie_stock","symbols":["BK1141","BK1576","BK1583","159837","03347"],"gpt_icon":0},{"id":"2528737838","title":"信達生物醫藥科技（杭州）有限公司藥品申請臨牀試驗默示許可獲受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2528737838","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528737838?lang=zh_tw&edition=fundamental","pubTime":"2025-04-17 12:16","pubTimestamp":1744863388,"startTime":"0","endTime":"0","summary":"4月17日，据CDE官网消息，信达生物医药科技（杭州）有限公司联合申请药品“IBI3020”，获得临床试验默示许可，受理号CXSL2500123。公示信息显示，药品“IBI3020”适应症：不可切除、局部晚期或转移性实体瘤。信达生物医药科技（杭州）有限公司，成立于2024年，位于杭州市，是一家以从事研究和试验发展为主的企业。企业注册资本70万美元。通过天眼查大数据分析，信达生物医药科技（杭州）有限公司专利信息3条。主要股东信息显示，信达生物医药科技（杭州）有限公司由Innovent Biologics (HK) Limited持股100%。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/17121649612042.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["03347","BK1141","09939","BK1161","LU2488822045.USD","BK1589","LU1969619763.USD","BK1576","159938","BK1583","BK1574","BK1515","LU2328871848.SGD","01801"],"gpt_icon":0},{"id":"2528673784","title":"江西銀濤藥業股份有限公司藥品申請臨牀試驗默示許可獲受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2528673784","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528673784?lang=zh_tw&edition=fundamental","pubTime":"2025-04-17 12:16","pubTimestamp":1744863388,"startTime":"0","endTime":"0","summary":"4月17日，据CDE官网消息，江西银涛药业股份有限公司联合申请药品“反流清颗粒”，获得临床试验默示许可，受理号CXZL2500005。江西银涛药业股份有限公司，成立于2001年，位于抚州市，是一家以从事医药制造业为主的企业。通过天眼查大数据分析，江西银涛药业股份有限公司共对外投资了6家企业，参与招投标项目5000次，知识产权方面有商标信息23条，专利信息79条，此外企业还拥有行政许可19个。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/17121649612040.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["BK1576","03347","BK1141","BK1583"],"gpt_icon":0},{"id":"2528874737","title":"武漢人福創新藥物研發中心有限公司藥品申請臨牀試驗默示許可獲受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2528874737","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528874737?lang=zh_tw&edition=fundamental","pubTime":"2025-04-17 12:16","pubTimestamp":1744863387,"startTime":"0","endTime":"0","summary":"4月17日，据CDE官网消息，武汉人福创新药物研发中心有限公司联合申请药品“HWS116注射液”，获得临床试验默示许可，受理号CXSL2500125。公示信息显示，药品“HWS116注射液”适应症：晚期实体瘤。武汉人福创新药物研发中心有限公司，成立于2020年，位于武汉市，是一家以从事研究和试验发展为主的企业。企业注册资本2000万人民币，实缴资本2000万人民币。通过天眼查大数据分析，武汉人福创新药物研发中心有限公司专利信息132条，此外企业还拥有行政许可3个。主要股东信息显示，武汉人福创新药物研发中心有限公司由人福医药集团股份公司持股100%。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/17121649612043.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["BK1576","159992","BK1161","06978","03347","BK1141","BK1583","BK1574"],"gpt_icon":0},{"id":"2527649682","title":"泰格醫藥收盤下跌2.37%，滾動市盈率93.04倍，總市值376.94億元","url":"https://stock-news.laohu8.com/highlight/detail?id=2527649682","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527649682?lang=zh_tw&edition=fundamental","pubTime":"2025-04-16 17:41","pubTimestamp":1744796473,"startTime":"0","endTime":"0","summary":"4月16日，泰格医药今日收盘43.58元，下跌2.37%，滚动市盈率PE达到93.04倍，总市值376.94亿元。从行业市盈率排名来看，公司所处的医疗服务行业市盈率平均45.05倍，行业中值46.97倍，泰格医药排名第38位。资金流向方面，4月16日，泰格医药主力资金净流出921.77万元，近5日总体呈流入状态，5日共流入4385.71万元。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/16174149587779.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["300347","BK1576","LU1146622755.USD","BK1141","BK1583","LU1820825898.SGD","BK0077","03347","BK0174","BK0028","BK0216"],"gpt_icon":0},{"id":"2527041255","title":"衞信康(603676.SH)子公司琥珀酰明膠電解質醋酸鈉注射液獲批臨牀試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2527041255","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527041255?lang=zh_tw&edition=fundamental","pubTime":"2025-04-16 15:32","pubTimestamp":1744788774,"startTime":"0","endTime":"0","summary":"智通财经APP讯，卫信康 发布公告，近日，公司全资子公司内蒙古白医制药股份有限公司收到国家药品监督管理局核准签发的琥珀酰明胶电解质醋酸钠注射液《药物临床试验批准通知书》。公司全资子公司白医制药申报的琥珀酰明胶电解质醋酸钠注射液是以 B.Braun Melsungen AG 持证的 Succinylated Gelatin Electrolytes Injection 为参比制剂开发，本品作为溶解在等渗电解质平衡型溶液中的胶体血浆容量代用品，用于：1、相对或绝对的低血容量及休克的治疗。","market":"hk","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/1279422.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":["03347","BK1583","BK1576","603676","BK0239","BK0191","BK1141"],"gpt_icon":0},{"id":"2527297099","title":"翰森製藥（3692.HK）自主研發的靶向KRAS G12D小分子1類新藥HS-10529片獲NMPA簽發的藥物臨牀試驗批准通知書","url":"https://stock-news.laohu8.com/highlight/detail?id=2527297099","media":"IR之家","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527297099?lang=zh_tw&edition=fundamental","pubTime":"2025-04-16 14:01","pubTimestamp":1744783305,"startTime":"0","endTime":"0","summary":"4月15日，翰森制药集团有限公司宣布，其自主研发的靶向KRAS G12D小分子1类新药HS-10529片获中国国家药品监督管理局签发的药物临床试验批准通知书，拟开展用于KRAS G12D突变的晚期实体瘤的临床。上述六大治疗领域2018年合计占中国药品总销售额的62.5%，增长快于整体中国医药行业，2014年至2018年平均增长8.1%。","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=nesSN20250416183144a45afda1&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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