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03347 泰格医药
已收盘 05-12 16:08:12
27.300
+0.600
+2.25%
最高
27.350
最低
26.350
成交量
174.69万
今开
26.850
昨收
26.700
日振幅
3.75%
总市值
236.15亿
流通市值
33.58亿
总股本
8.65亿
成交额
4,695万
换手率
1.42%
流通股本
1.23亿
市净率
--
ROE
--
每股收益
0.00
52周最高
--
52周最低
--
市盈率
--
股息
--
股息收益率
--
ROA
--
分时
五日
日K
周K
月K
数据加载中...
北京优虎网络科技有限公司
免责声明:香港交易所资讯服务有限公司、其控股公司及/或该等控股公司的任何附属公司均竭力确保所提供信息的准确和可靠度,但不能保证其绝对准确和可靠,且亦不会承担因任何不准确或遗漏而引起的任何损失或损害的责任(不管是否侵权法下的责任或合约责任又或其它责任)
资讯
新帖
简况
荣昌生物(688331.SH):抗体偶联药物RC278获得药物临床试验申请受理通知书
智通财经 · 15:51
荣昌生物(688331.SH):抗体偶联药物RC278获得药物临床试验申请受理通知书
荣昌生物:抗体偶联药物RC278临床试验申请获受理
美港电讯 · 15:40
荣昌生物:抗体偶联药物RC278临床试验申请获受理
百诚医药:BIOS-0618临床试验顺利,2025年4月已获得适用于新增适应症阻塞性睡眠呼吸暂停综合征患者日间过度思睡治疗的临床试验批件
证券之星 · 15:07
百诚医药:BIOS-0618临床试验顺利,2025年4月已获得适用于新增适应症阻塞性睡眠呼吸暂停综合征患者日间过度思睡治疗的临床试验批件
港股异动 | 生物医药股持续回调,特朗普拟将药价立即降低30%-80%
老虎资讯综合 · 10:11
港股异动 | 生物医药股持续回调,特朗普拟将药价立即降低30%-80%
每周股票复盘:中恒集团(600252)回购进展与三芪颗粒临床试验获批
证券之星 · 05-10 02:06
每周股票复盘:中恒集团(600252)回购进展与三芪颗粒临床试验获批
每周股票复盘:恒瑞医药(600276)多个药物获临床试验批准
证券之星 · 05-10 01:03
每周股票复盘:恒瑞医药(600276)多个药物获临床试验批准
广生堂:GST-HG131联合GST-HG141的II期临床试验申请已获得批准
证券之星 · 05-09 20:52
广生堂:GST-HG131联合GST-HG141的II期临床试验申请已获得批准
智飞生物(300122.SZ):四价流感病毒裂解疫苗(ZFA02佐剂)进入Ⅰ/Ⅱ期临床试验
智通财经 · 05-09 19:48
智飞生物(300122.SZ):四价流感病毒裂解疫苗(ZFA02佐剂)进入Ⅰ/Ⅱ期临床试验
智飞生物:佐剂四价流感疫苗进入Ⅰ/Ⅱ期临床试验
美港电讯 · 05-09 19:41
智飞生物:佐剂四价流感疫苗进入Ⅰ/Ⅱ期临床试验
智飞生物最新公告:四价流感病毒裂解疫苗(ZFA02佐剂)进入Ⅰ/Ⅱ期临床试验
证券之星 · 05-09 19:39
智飞生物最新公告:四价流感病毒裂解疫苗(ZFA02佐剂)进入Ⅰ/Ⅱ期临床试验
乐普医疗最新公告:子公司MWN109片获得药物临床试验批准通知书
证券之星 · 05-09 19:20
乐普医疗最新公告:子公司MWN109片获得药物临床试验批准通知书
石药集团1类新药SYH2046获FDA批准开展临床试验
财中社 · 05-09 19:01
石药集团1类新药SYH2046获FDA批准开展临床试验
复星医药(02196)附属菌济健康获美国 FDA 药品临床试验批准
智通财经 · 05-09 18:48
复星医药(02196)附属菌济健康获美国 FDA 药品临床试验批准
恒瑞医药(600276.SH):SHR-1316(sc)注射液获得药物临床试验批准通知书
智通财经 · 05-09 17:55
恒瑞医药(600276.SH):SHR-1316(sc)注射液获得药物临床试验批准通知书
恒瑞医药最新公告:子公司收到7项药物临床试验批准通知书
证券之星 · 05-09 17:50
恒瑞医药最新公告:子公司收到7项药物临床试验批准通知书
恒瑞医药最新公告:子公司收到SHR-1316(sc)注射液临床试验批准通知书
证券之星 · 05-09 17:50
恒瑞医药最新公告:子公司收到SHR-1316(sc)注射液临床试验批准通知书
复星医药最新公告:控股子公司菌济健康获美国FDA药品临床试验批准
证券之星 · 05-09
复星医药最新公告:控股子公司菌济健康获美国FDA药品临床试验批准
复星医药子公司获美国FDA批准开展AGA治疗临床试验
财中社 · 05-09
复星医药子公司获美国FDA批准开展AGA治疗临床试验
每日卖空追踪 | 泰格医药 05月09日卖空量成交4.89万股,卖空比例为6.29%
市场透视 · 05-09
每日卖空追踪 | 泰格医药 05月09日卖空量成交4.89万股,卖空比例为6.29%
复星医药(600196.SH)控股子公司获美国FDA药品临床试验批准
智通财经 · 05-09
复星医药(600196.SH)控股子公司获美国FDA药品临床试验批准
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公司概况
公司名称:
泰格医药
所属市场:
SEHK
上市日期:
--
主营业务:
杭州泰格医药科技股份有限公司是一家从事为新药研发提供临床试验服务的中国控股公司。该公司经营两个分部。临床试验技术服务分部向生物制药和医疗器械公司提供临床试验运作服务和医学翻译等服务,帮助其进行创新药物、仿制药和医疗器械的临床试验。临床试验相关服务及实验室服务分部从事提供分析服务,比如数据管理和统计分析;后勤和执行支持服务,比如临床试验现场管理;行政协助,比如患者招募;以及咨询服务等。该分部同时通过其子公司为临床前和临床开发阶段提供实验室服务。该公司在国内市场和海外市场开展业务。
发行价格:
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15:51","pubTimestamp":1747036312,"startTime":"0","endTime":"0","summary":"智通财经APP讯,荣昌生物(688331.SH)发布公告,近日,公司收到国家药品监督管理局核准签发的《受理通知书》,新型抗体偶联(ADC)药物注射用RC278的临床试验申请获得受理。RC278是由荣昌生物自主研发的一款具有First-in-Class/Best-in-Class潜质的ADC分子,该分子能特异识别一个新型肿瘤靶点,并具有创新的连接子—毒素系统,在临床前研究中展现出广谱抗肿瘤活性、良好的安全性和药代动力学特征,将为晚期实体瘤患者带来新的治疗选择。","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/1291947.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":["BK1583","LU1064131003.USD","BK1141","BK1576","09995","BK1574","LU1064130708.USD","LU2148510915.USD","LU1969619763.USD","03347","LU2328871848.SGD","BK0239","BK1161","688331"],"gpt_icon":0},{"id":"2534321815","title":"荣昌生物:抗体偶联药物RC278临床试验申请获受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2534321815","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2534321815?lang=zh_cn&edition=full","pubTime":"2025-05-12 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15:07","pubTimestamp":1747033642,"startTime":"0","endTime":"0","summary":"证券之星消息,百诚医药(301096)05月12日在投资者关系平台上答复投资者关心的问题。投资者提问:董秘你好,请问百诚医药1类药BIOS-0618片新批的临床试验进展如何,是否符合预期?百诚医药回复:尊敬的投资者您好,BIOS-0618临床试验顺利,2025年4月已获得适用于新增适应症阻塞性睡眠呼吸暂停综合征(OSA)患者日间过度思睡治疗的临床试验批件,后续相关进展请关注公司定期报告,感谢您的关注。以上内容为证券之星据公开信息整理,由AI算法生成(网信算备310104345710301240019号),不构成投资建议。","market":"fut","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://stock.stockstar.com/RB2025051200013839.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":"stockstar","symbols":["BK1141","BK1583","BK0216","03347","301096","BK1576"],"gpt_icon":0},{"id":"1181990888","title":"港股异动 | 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均跌超6%:消息面上,美国总统特朗普称,将在白宫签署行政命令。处方药和药品价格几乎将立即降低30%至80%,美国将以全球最低价格国家的价格购买药品。","market":"hk","thumbnail":"https://static.tigerbbs.com/85675909dc6c67ee0181339c18bcfdff","type":0,"news_type":0,"thumbnails":["https://static.tigerbbs.com/85675909dc6c67ee0181339c18bcfdff"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":true,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["02696","02269","02359","03347","06622","09995","00241","06606","03759","06185","603259","01801","06160","06996","06127","06618","WX"],"gpt_icon":0},{"id":"2534459027","title":"每周股票复盘:中恒集团(600252)回购进展与三芪颗粒临床试验获批","url":"https://stock-news.laohu8.com/highlight/detail?id=2534459027","media":"证券之星","labels":["shareholding","buyback"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2534459027?lang=zh_cn&edition=full","pubTime":"2025-05-10 02:06","pubTimestamp":1746813977,"startTime":"0","endTime":"0","summary":"截至2025年5月9日收盘,中恒集团报收于2.47元,较上周的2.43元上涨1.65%。本周,中恒集团5月8日盘中最高价报2.51元。5月6日盘中最低价报2.42元。中恒集团当前最新总市值81.84亿元,在中药板块市值排名28/69,在两市A股市值排名1884/5145。基于《中药注册管理专门规定》中“三结合”的审评证据体系,获批豁免Ⅰ期临床试验。三芪颗粒获得药物临床试验批准有望为中恒集团进入市场广阔的慢性肾病领域奠定基础。","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":"https://stock.stockstar.com/RB2025051000001492.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"shareholding,buyback","news_rank":0,"length":0,"strategy_id":0,"source":"stockstar","symbols":["600252","BK0012","BK1141","BK0028","BK0015","BK0188","03347","BK1576","BK1583","BK0239","BK0077"],"gpt_icon":0},{"id":"2534745587","title":"每周股票复盘:恒瑞医药(600276)多个药物获临床试验批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2534745587","media":"证券之星","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2534745587?lang=zh_cn&edition=full","pubTime":"2025-05-10 01:03","pubTimestamp":1746810198,"startTime":"0","endTime":"0","summary":"截至2025年5月9日收盘,恒瑞医药报收于52.81元,较上周的51.1元上涨3.35%。根据我国药品注册相关的法律法规要求,药物在获得药物临床试验批准通知书后,尚需开展临床试验并经国家药监局审评、审批通过后方可生产上市。","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":"https://stock.stockstar.com/RB2025051000001141.shtml","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":"stockstar","symbols":["BK0196","BK0239","LU2488822045.USD","BK0060","LU1969619763.USD","600276","03347","LU2148510915.USD","LU1064131003.USD","BK0012","LU2328871848.SGD","BK1583","BK0183","BK1576","BK0188","LU1328615791.USD","BK1141","LU0405327148.USD","LU0405327494.USD","LU1064130708.USD","BK0028"],"gpt_icon":0},{"id":"2534348178","title":"广生堂:GST-HG131联合GST-HG141的II期临床试验申请已获得批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2534348178","media":"证券之星","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2534348178?lang=zh_cn&edition=full","pubTime":"2025-05-09 20:52","pubTimestamp":1746795153,"startTime":"0","endTime":"0","summary":"GST-HG131为表面抗原抑制剂,GST-HG141为核衣壳调节剂,二者都是广生堂乙肝登峰计划的重要组成部分。基于GST-HG131和GST-HG141的临床前研究和已披露的临床研究结果,GST-HG131对HBsAg具有明显抑制作用,GST-HG141片对HBV DNA有显著的抑制效应且明显降低pgRNA,间接体现了对HBV cccDNA 的潜在有效抑制和耗竭作用,两者在抗病毒机制上预计协同互补。GST-HG131 联合 GST-HG141 的 II 期临床试验申请已获得批准,旨在探索基于核苷(酸)类似物基础治疗上,GST-HG131片联合GST-HG141片,三联全口服用药挑战乙肝临床治愈。","market":"fut","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://stock.stockstar.com/RB2025050900037830.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stockstar","symbols":["BK1583","03347","BK1576","300436","BK0239","BK1141"],"gpt_icon":0},{"id":"2534483441","title":"智飞生物(300122.SZ):四价流感病毒裂解疫苗(ZFA02佐剂)进入Ⅰ/Ⅱ期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2534483441","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2534483441?lang=zh_cn&edition=full","pubTime":"2025-05-09 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19:20","pubTimestamp":1746789657,"startTime":"0","endTime":"0","summary":"乐普医疗(300003.SZ)公告称,公司收到国家药品监督管理局核准签发的《药物临床试验批准通知书》,由民为生物申报的MWN109片临床试验申请获得批准。MWN109片是乐普医疗自主研发的GLP-1/GIP/GCG活性脂肪酸链修饰多肽药物的口服剂型,适应症包括2型糖尿病和超重或肥胖。不过,该在研项目尚处于研发早期阶段,存在结果不确定性高、研发投入大、临床试验周期长等特点,以及临床试验失败、审评审批失败和竞争加剧等风险。以上内容为证券之星据公开信息整理,由AI算法生成(网信算备310104345710301240019号),不构成投资建议。","market":"fut","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://stock.stockstar.com/RB2025050900033831.shtml","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":"stockstar","symbols":["BK0188","BK0196","BK1141","300003","BK1583","BK0114","BK0201","BK0042","BK0028","BK0251","BK1576","BK0113","03347"],"gpt_icon":0},{"id":"2534100774","title":"石药集团1类新药SYH2046获FDA批准开展临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2534100774","media":"财中社","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2534100774?lang=zh_cn&edition=full","pubTime":"2025-05-09 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亿元(未经审计)。","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/1291488.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK0188","03347","BK0175","BK0060","600196","BK0096","BK0239","BK0187","BK0183","BK0196","BK0028","BK1593","02196","BK1515","BK1583","BK0012","BK1576","BK1141","BK1191"],"gpt_icon":0},{"id":"2534177637","title":"恒瑞医药(600276.SH):SHR-1316(sc)注射液获得药物临床试验批准通知书","url":"https://stock-news.laohu8.com/highlight/detail?id=2534177637","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2534177637?lang=zh_cn&edition=full","pubTime":"2025-05-09 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16:37","pubTimestamp":1746779855,"startTime":"0","endTime":"0","summary":"5月9日,复星医药发布公告,控股子公司菌济健康获得美国FDA关于LBP-ShC4开展临床试验的批准。公告指出,目前全球尚无用于治疗雄激素脱发的活体生物治疗产品获批上市。尽管获得临床试验批准,但药品研发存在风险,后续的临床研究仍需获得美国药品审评部门的审批,且临床试验可能因安全性和有效性问题而终止。2025年一季度,复星医药实现收入94.20亿元,归母净利润7.65亿元。","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=nesSN20250509164519a477e291&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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