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泰格医药
27.200
+0.450
1.68%
手动刷新
成交量:
73.46万
成交额:
1,925.60万
市值:
235.27亿
市盈率:
53.91
高:
27.250
开:
26.600
低:
25.400
收:
26.750
数据加载中...
总览
公司
新闻
公告
Sands Capital Management,LP减持泰格医药(03347)38.41万股 每股作价为25.9329港元
智通财经
·
04-18
【沃森生物:20价肺炎球菌多糖结合疫苗获临床试验批准】沃森生物公告,公司及子公司共同申请的20价肺炎球菌多糖结合疫苗获得国家药品监督管理局签发的《药物临床试验批准通知书》,通知书编号为2025LP01099。该疫苗是在已上市产品13价肺炎球菌多糖结合疫苗基础上开发的迭代升级产品,新增了8型、10A型、11A型、12F型、15B型、22F型和33F型共计7种血清型,用于预防由本品所含20种肺炎球菌血清型引起的感染性疾病。全球已上市20价肺炎球菌多糖结合疫苗的厂家仅有美国辉瑞公司一家,国内尚未有20价肺炎球菌多糖结合疫苗上市销售。
金融界
·
04-18
盛禾(中国)生物制药有限公司药品申请临床试验默示许可获受理
金融界
·
04-18
石药集团欧意药业有限公司药品申请临床试验默示许可获受理
金融界
·
04-18
普方生物制药(苏州)有限公司药品申请临床试验默示许可获受理
金融界
·
04-18
江苏华益科技有限公司药品申请临床试验默示许可获受理
金融界
·
04-18
兆科眼科-B(06622):环孢素A眼凝胶新一轮第III期临床试验入组首名患者
智通财经
·
04-17
南京维立志博生物科技股份有限公司药品申请临床试验默示许可获受理
金融界
·
04-17
信达生物医药科技(杭州)有限公司药品申请临床试验默示许可获受理
金融界
·
04-17
江西银涛药业股份有限公司药品申请临床试验默示许可获受理
金融界
·
04-17
武汉人福创新药物研发中心有限公司药品申请临床试验默示许可获受理
金融界
·
04-17
泰格医药收盘下跌2.37%,滚动市盈率93.04倍,总市值376.94亿元
金融界
·
04-16
卫信康(603676.SH)子公司琥珀酰明胶电解质醋酸钠注射液获批临床试验
智通财经
·
04-16
翰森制药(3692.HK)自主研发的靶向KRAS G12D小分子1类新药HS-10529片获NMPA签发的药物临床试验批准通知书
IR之家
·
04-16
泰格医药盘中异动 急速下挫5.00%
市场透视
·
04-16
【华泰证券:AI医疗产业趋势正在加速】华泰证券研报表示,4月10日,美国FDA宣布将通过一系列方法减少、改进或取代在单克隆抗体疗法及其他药物的研发中动物试验要求,包括基于AI的毒性计算模型、在实验室环境中进行的细胞系和类器官毒性测试。2025年计划启动试点项目,允许部分药企在FDA监督下完全跳过动物实验,全面政策更新预计2026年完成。FDA此项政策将进一步推动AI在新药研发中的覆盖,从化学合成环节加速走向临床前及临床试验等生物环节,推动创新药企业加大AI药物发现平台投入。再次强调2025年“AI+医疗”将迎来跨越式发展,应重视相关投资机会。
金融界
·
04-16
映恩生物登陆港交所首日大涨116.70%;百利天恒第10款ADC获批临床试验 | 医药早参
每日经济新闻
·
04-16
【翰森制药HS-10529获批临床,拟治疗KRAS G12D突变晚期实体瘤】 4月15日,翰森制药宣布,公司自主研发的1类新药HS-10529片获国家药品监督管理局签发的药物临床试验批准通知书,拟开发治疗KRAS G12D突变的晚期实体瘤。
金融界
·
04-16
翰森制药(03692.HK)HS-10529片药物临床试验获批
阿斯达克财经
·
04-16
翰森制药(03692):HS-10529片获国家药品监督管理局签发的药物临床试验批准通知书
智通财经
·
04-15
更多
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Capital Management,LP减持泰格医药(03347)38.41万股 每股作价为25.9329港元","url":"https://stock-news.laohu8.com/highlight/detail?id=2528064691","media":"智通财经","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528064691?lang=zh_cn&edition=fundamental","pubTime":"2025-04-18 21:17","pubTimestamp":1744982239,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,香港联交所最新资料显示,4月15日,Sands Capital Management,LP减持泰格医药(03347)38.41万股,每股作价为25.9329港元,总金额约为996.08万港元。减持后最新持股数目为1089.6493万股,持股比例为8.85%。本交易涉及其他关联方:Sands Capital Management,LLC;Sands Family Trust, LLC;Sands Frank Melville 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19:21","pubTimestamp":1744975312,"startTime":"0","endTime":"0","summary":"沃森生物公告,公司及子公司共同申请的20价肺炎球菌多糖结合疫苗获得国家药品监督管理局签发的《药物临床试验批准通知书》,通知书编号为2025LP01099。该疫苗是在已上市产品13价肺炎球菌多糖结合疫苗基础上开发的迭代升级产品,新增了8型、10A型、11A型、12F型、15B型、22F型和33F型共计7种血清型,用于预防由本品所含20种肺炎球菌血清型引起的感染性疾病。全球已上市20价肺炎球菌多糖结合疫苗的厂家仅有美国辉瑞公司一家,国内尚未有20价肺炎球菌多糖结合疫苗上市销售。","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://24h.jrj.com.cn/2025/04/18192149669574.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":["LU1066051498.USD","LU0225284248.USD","BK0070","LU1057294990.SGD","IE00BBT3K403.USD","LU0170899867.USD","LU0234572021.USD","LU0306806265.USD","SG9999003800.SGD","BK4581","BK0239","LU0225771236.USD","LU1894683348.USD","SG9999002224.SGD","LU0058720904.USD","IE0002270589.USD","IE000M9KFDE8.USD","LU0321505439.SGD","SG9999001176.USD","BK0077","LU1883839398.USD","BK4568","BK1141","SG9999001176.SGD","IE00B19Z3B42.SGD","BK4550","LU0289739699.SGD","LU0456855351.SGD","300142","LU0306807586.USD","LU0985481810.HKD","SG9999002232.USD","BK4585","IE00BLSP4239.USD","SG9999013999.USD","BK4592","BK1576","SG9999011175.SGD","SGXZ57979304.SGD","BK4534","LU1066053197.SGD","159646","LU1894683264.USD","BK4007","BK4599","IE00BLSP4452.SGD","BK4533","03347","LU1023059063.AUD"],"gpt_icon":0},{"id":"2528872920","title":"盛禾(中国)生物制药有限公司药品申请临床试验默示许可获受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2528872920","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528872920?lang=zh_cn&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,盛禾(中国)生物制药有限公司联合申请药品“IAH0968”,获得临床试验默示许可,受理号CXSL2500141。盛禾(中国)生物制药有限公司,成立于2018年,位于南京市,是一家以从事医药制造业为主的企业。主要股东信息显示,盛禾(中国)生物制药有限公司由盛禾医药科技有限公司持股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/2025/04/18134049650526.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","BK1576","BK1141","BK1583"],"gpt_icon":0},{"id":"2528308722","title":"石药集团欧意药业有限公司药品申请临床试验默示许可获受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2528308722","media":"金融界","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528308722?lang=zh_cn&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,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":"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/2025/04/18134049650524.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":["BK1515","LU0880133367.SGD","LU1152091168.USD","IE00BZ08YR35.GBP","SG9999004220.SGD","BK1141","LU1993786604.SGD","IE00B5MMRT66.SGD","LU0072913022.USD","01093","LU1807302812.USD","IE00BZ08YS42.EUR","LU0067412154.USD","IE00BZ08YT58.USD","LU0501845795.SGD","IE00B543WZ88.USD","IE0008369823.USD","LU1226287875.USD","IE00B031HY20.USD","LU1226287529.USD","LU1960683339.HKD","LU1008478684.HKD","LU1226288253.USD","BK1583","LU0140636845.USD","LU1226287792.SGD","LU1226288170.HKD","BK1521","BK1191","IE0008368742.USD","03347","BK1576","LU1152091754.HKD","LU1951186391.HKD","LU0326950275.SGD"],"gpt_icon":0},{"id":"2528208778","title":"普方生物制药(苏州)有限公司药品申请临床试验默示许可获受理","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_cn&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":"江苏华益科技有限公司药品申请临床试验默示许可获受理","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_cn&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):环孢素A眼凝胶新一轮第III期临床试验入组首名患者","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_cn&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":"南京维立志博生物科技股份有限公司药品申请临床试验默示许可获受理","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_cn&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":"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/2025/04/17121649612041.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":["159837","BK1576","BK1583","03347","BK1141"],"gpt_icon":0},{"id":"2528737838","title":"信达生物医药科技(杭州)有限公司药品申请临床试验默示许可获受理","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_cn&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":"江西银涛药业股份有限公司药品申请临床试验默示许可获受理","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_cn&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":"武汉人福创新药物研发中心有限公司药品申请临床试验默示许可获受理","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_cn&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":"泰格医药收盘下跌2.37%,滚动市盈率93.04倍,总市值376.94亿元","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_cn&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":"卫信康(603676.SH)子公司琥珀酰明胶电解质醋酸钠注射液获批临床试验","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_cn&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":"翰森制药(3692.HK)自主研发的靶向KRAS G12D小分子1类新药HS-10529片获NMPA签发的药物临床试验批准通知书","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_cn&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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