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泰格医药

25.850

-0.700-2.64%

成交量：354.76万

成交额：9,277.14万

市值：223.59亿

市盈率：51.59

高：26.650

开：26.000

低：25.500

收：26.550

数据加载中...

总览公司新闻公告

【新诺威：SYS6041抗体偶联药物获美国临床试验批准】新诺威公告，控股子公司巨石生物申报的SYS6041注射剂临床试验申请已获得美国FDA批准，可以在美国开展临床试验。该药物是一款单克隆抗体偶联药物，适用于晚期实体瘤，已在国内外提交多件专利申请。此前，该产品已于2025年1月获得中国国家药品监督管理局批准，可以在中国开展临床试验。

泰格医药04月14日获主力加仓323万元

恒瑞医药(600276.SH)子公司多款药品获药物临床试验批准通知书

智通财经网

恒瑞医药(600276.SH)：SHR-1819注射液获得药物临床试验批准通知书

恒瑞医药(600276.SH)SHR-1819注射液获药物临床试验批准通知书

智通财经网

恒瑞医药(600276.SH)：获得药物临床试验批准通知书

恩华药业(002262.SZ)：NH280105在澳大利亚启动I期临床试验并完成首例受试者入组和给药

【恩华药业：NH280105在澳大利亚启动I期临床试验并完成首例受试者入组和给药】恩华药业公告，公司全资子公司上海枢境生物科技有限公司近日收到澳大利亚人类研究伦理委员会签发的批准NH280105胶囊开展I期临床试验的临床试验伦理许可，并已向澳大利亚药品管理局（TGA）进行临床试验备案。NH280105是一种口服高选择性Lp-PLA2抑制剂，拟用于阿尔茨海默病的治疗。该药物通过抑制Lp-PLA2，减少炎症反应并修复血脑屏障，改善患者的认知功能。本次临床试验为NH280105首次在人类受试者中开展的I期临床试验，旨在评估健康成人受试者单次和多次口服NH280105胶囊的安全性、耐受性和药代动力学特征。

港股异动 | 石药集团(01093)涨超5% SYH2046片获中国临床试验批准

智通财经网

博雅生物拟挂牌转让子公司80%股权；恒瑞医药两款药物获批临床试验｜医药早参

每日经济新闻

石药集团(01093.HK)SYH2046片获准开展临床试验

阿斯达克财经

恒瑞医药(600276.SH)：注射用HRS-9190获得药物临床试验批准通知书

智通财经网

恒瑞医药(600276.SH)：SHR-3792注射液获批开展晚期实体瘤的临床试验

兆科眼科-B：BRIMOCHOLPF第II期临床试验入组首名患者

石药集团(01093)：SYH2046片获中国临床试验批准

兆科眼科(06622.HK)治疗老花眼药物II期临床试验入组首名患者另与Lunatus就药物订立分销协议

阿斯达克财经

常山药业(300255.SZ)：艾本那肽注射液临床试验申请获受理

兆科眼科-B(06622)：BRIMOCHOL™PF第II期临床试验入组首名患者

汇宇制药：注射用HY0001a药物临床试验申请获受理

汇宇制药(688553.SH)：注射用HY0001a获得药物临床试验申请受理通知书

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16:16","pubTimestamp":1744618576,"startTime":"0","endTime":"0","summary":"04月14日, 泰格医药股价涨2.46%，报收27.05元，成交金额5595万元，换手率1.69%，振幅3.79%，量比0.48。泰格医药今日主力资金净流入323万元，上一交易日主力净流入675万元。该股近5个交易日上涨10.82%，主力资金累计净流入716万元；近20日主力资金累计净流出3706万元，其中净流出天数为11日。","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=nesSN20250414171026a6b9da50&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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16:13","pubTimestamp":1744618380,"startTime":"0","endTime":"0","summary":"恒瑞医药公告，近日，公司子公司山东盛迪医药有限公司、苏州盛迪亚生物医药有限公司、上海盛迪医药有限公司收到国家药品监督管理局核准签发关于HRS-7058胶囊/片、阿得贝利单抗注射液、贝伐珠单抗注射液和注射用SHR-1826的《药物临床试验批准通知书》，将于近期开展临床试验。注射用SHR-1826是一款以c-MET为靶点的抗体偶联药物，通过与肿瘤细胞表面的靶抗原特异性结合，被内吞进入肿瘤细胞后杀伤肿瘤细胞。","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://finance.sina.com.cn/stock/hkstock/ggscyd/2025-04-14/doc-inetcqhr4983944.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":"sina","symbols":["BK0060","BK1141","LU1064130708.USD","BK0239","600276","LU1969619763.USD","BK1583","LU1328615791.USD","LU2148510915.USD","LU2328871848.SGD","BK0183","BK1576","LU0405327148.USD","LU1064131003.USD","LU0405327494.USD","BK0028","BK0196","03347","BK0188","BK0012","LU2488822045.USD"],"gpt_icon":0},{"id":"2527901222","title":"恒瑞医药(600276.SH)：SHR-1819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=2527901222","media":"格隆汇","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527901222?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 16:09","pubTimestamp":1744618169,"startTime":"0","endTime":"0","summary":"格隆汇4月14日丨恒瑞医药(600276.SH)公布，公司子公司广东恒瑞医药有限公司收到国家药品监督管理局核准签发关于SHR-1819注射液的《药物临床试验批准通知书》，将于近期开展临床试验。SHR-1819注射液是公司自主研发的一种靶向人IL-4Rα的重组人源化单克隆抗体，能够同时阻断IL-4和IL-13的信号传导，拟用于治疗2型炎症相关疾病。","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/2025/04/14160949518339.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":["BK0188","BK0012","LU1328615791.USD","LU1969619763.USD","LU0405327148.USD","BK1576","LU2328871848.SGD","BK0196","BK1141","LU1064131003.USD","BK1583","BK0028","BK0239","600276","BK0183","LU1064130708.USD","LU2148510915.USD","BK0060","LU0405327494.USD","LU2488822045.USD","03347"],"gpt_icon":0},{"id":"2527125184","title":"恒瑞医药(600276.SH)SHR-1819注射液获药物临床试验批准通知书","url":"https://stock-news.laohu8.com/highlight/detail?id=2527125184","media":"智通财经网","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527125184?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 16:09","pubTimestamp":1744618140,"startTime":"0","endTime":"0","summary":"恒瑞医药(600276.SH)公告，近日，公司子公司广东恒瑞医药有限公司收到国家药品监督管理局(简称“国家药监局”)核准签发关于SHR-1819注射液的《药物临床试验批准通知书》，将于近期开展临床试验。根据《中华人民共和国药品管理法》及有关规定，经审查，2025年1月26日受理的SHR-1819注射液临床试验申请符合药品注册的有关要求，同意本品开展过敏性鼻炎的临床试验。\n\n\n\n海量资讯、精准解读，尽在新浪财经APP","market":"other","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://finance.sina.com.cn/stock/hkstock/ggscyd/2025-04-14/doc-inetcqhu8740399.shtml","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":"sina","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":"2527901040","title":"恒瑞医药(600276.SH)：获得药物临床试验批准通知书","url":"https://stock-news.laohu8.com/highlight/detail?id=2527901040","media":"格隆汇","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527901040?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 16:08","pubTimestamp":1744618118,"startTime":"0","endTime":"0","summary":"格隆汇4月14日丨恒瑞医药(600276.SH)公布，公司子公司山东盛迪医药有限公司、苏州盛迪亚生物医药有限公司、上海盛迪医药有限公司收到国家药品监督管理局核准签发关于HRS-7058胶囊/片、阿得贝利单抗注射液、贝伐珠单抗注射液和注射用SHR-1826的《药物临床试验批准通知书》，将于近期开展临床试验。","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/2025/04/14160849518344.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["BK0188","LU1969619763.USD","600276","BK1141","BK0239","LU0405327494.USD","LU1064130708.USD","BK0028","LU2488822045.USD","LU1064131003.USD","BK1576","BK0060","LU0405327148.USD","03347","BK0196","LU2148510915.USD","BK1583","LU2328871848.SGD","LU1328615791.USD","BK0183","BK0012"],"gpt_icon":0},{"id":"2527906407","title":"恩华药业(002262.SZ)：NH280105在澳大利亚启动I期临床试验并完成首例受试者入组和给药","url":"https://stock-news.laohu8.com/highlight/detail?id=2527906407","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527906407?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 15:58","pubTimestamp":1744617481,"startTime":"0","endTime":"0","summary":"智通财经APP讯，恩华药业 公告，公司的全资子公司上海枢境生物科技有限公司于近日收到澳大利亚人类研究伦理委员会签发的批准NH280105胶囊开展I期临床试验的临床试验伦理许可，并已向澳大利亚药品管理局进行临床试验备案。按照澳大利亚药品注册相关法律法规，上海枢境于近日开展对该产品进行相关临床试验，并完成首例受试者入组和给药。其独特的作用机制使其有望成为阿尔茨海默病治疗的新选择。","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/1278087.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":["BK0239","BK0070","BK1576","BK0188","002262","03347","BK1583","BK1141"],"gpt_icon":0},{"id":"2527909867","title":"【恩华药业：NH280105在澳大利亚启动I期临床试验并完成首例受试者入组和给药】恩华药业公告，公司全资子公司上海枢境生物科技有限公司近日收到澳大利亚人类研究伦理委员会签发的批准NH280105胶囊开展I期临床试验的临床试验伦理许可，并已向澳大利亚药品管理局（TGA）进行临床试验备案。NH280105是一种口服高选择性Lp-PLA2抑制剂，拟用于阿尔茨海默病的治疗。该药物通过抑制Lp-PLA2，减少炎症反应并修复血脑屏障，改善患者的认知功能。本次临床试验为NH280105首次在人类受试者中开展的I期临床试验，旨在评估健康成人受试者单次和多次口服NH280105胶囊的安全性、耐受性和药代动力学特征。","url":"https://stock-news.laohu8.com/highlight/detail?id=2527909867","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527909867?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 15:55","pubTimestamp":1744617323,"startTime":"0","endTime":"0","summary":"恩华药业公告，公司全资子公司上海枢境生物科技有限公司近日收到澳大利亚人类研究伦理委员会签发的批准NH280105胶囊开展I期临床试验的临床试验伦理许可，并已向澳大利亚药品管理局（TGA）进行临床试验备案。NH280105是一种口服高选择性Lp-PLA2抑制剂，拟用于阿尔茨海默病的治疗。该药物通过抑制Lp-PLA2，减少炎症反应并修复血脑屏障，改善患者的认知功能。本次临床试验为NH280105首次在人类受试者中开展的I期临床试验，旨在评估健康成人受试者单次和多次口服NH280105胶囊的安全性、耐受性和药代动力学特征。","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://24h.jrj.com.cn/2025/04/14155549517905.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":"jinrongjie_stock","symbols":["BK0239","TGA","BK0188","03347","BK1141","159837","BK0070","BK4213","002262","BK1583","BK1576"],"gpt_icon":0},{"id":"2527494402","title":"港股异动 | 石药集团(01093)涨超5% SYH2046片获中国临床试验批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2527494402","media":"智通财经网","labels":["productRelease","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527494402?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 10:10","pubTimestamp":1744596600,"startTime":"0","endTime":"0","summary":"石药集团涨超5%，截至发稿，涨5.12%，报5.54港元，成交额2.45亿港元。消息面上，4月11日，石药集团宣布，集团开发的SYH2046片已获得国家药品监督管理局批准，可在中国开展临床试验。该产品是一款具有完全自主知识产权的全新结构first-in-class小分子药物，本次获批的临床试验适应症为急性心肌梗死后心力衰竭。临床前研究表明，该产品可显著改善疾病动物模型的心脏功能并降低心脏不良重构，且具有较高的安全性。","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://finance.sina.com.cn/stock/hkstock/marketalerts/2025-04-14/doc-inetaxma9008222.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease,movement","news_rank":0,"length":0,"strategy_id":0,"source":"sina","symbols":["LU1008478684.HKD","LU0501845795.SGD","LU1226287875.USD","LU1226288253.USD","03347","LU0067412154.USD","LU1993786604.SGD","IE0008369823.USD","BK1515","BK1521","SG9999004220.SGD","BK1191","LU0072913022.USD","IE00B543WZ88.USD","01093","IE00B031HY20.USD","IE00BZ08YR35.GBP","LU1152091754.HKD","IE00BZ08YS42.EUR","LU0326950275.SGD","LU0140636845.USD","LU0880133367.SGD","LU1226287792.SGD","LU1960683339.HKD","IE0008368742.USD","BK1141","LU1951186391.HKD","BK1583","IE00BZ08YT58.USD","LU1152091168.USD","LU1226288170.HKD","LU1807302812.USD","BK1576","IE00B5MMRT66.SGD","LU1226287529.USD"],"gpt_icon":0},{"id":"2527156359","title":"博雅生物拟挂牌转让子公司80%股权；恒瑞医药两款药物获批临床试验｜医药早参","url":"https://stock-news.laohu8.com/highlight/detail?id=2527156359","media":"每日经济新闻","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527156359?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 07:18","pubTimestamp":1744586306,"startTime":"0","endTime":"0","summary":"丨2025年4月14日星期一丨NO.1博雅生物拟公开挂牌转让子公司80%股权4月13日，博雅生物发布公告，称拟通过上海联合产权交易所挂牌转让江西博雅欣和制药有限公司（简称“博雅欣和”）80%股权，首次挂牌金额约为2.13亿元。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202504143375319785.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202504143375319785.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_eastmoney","symbols":["BK1515","BK1576","BK1161","BK1574","BK1141","03347","BK1583","09939"],"gpt_icon":0},{"id":"2527099963","title":"石药集团(01093.HK)SYH2046片获准开展临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2527099963","media":"阿斯达克财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527099963?lang=zh_cn&edition=fundamental","pubTime":"2025-04-13 19:12","pubTimestamp":1744542720,"startTime":"0","endTime":"0","summary":"石药集团(01093.HK) 公布，集团开发的SYH2046片获中国国家药品监督管理局批准，在内地开展临床试验。该产品是一款具有完全自主知识产权的全新结构first-in-class小分子药物，本次获批的临床试验适应症为急性心肌梗死后心力衰竭。(de/d)(港股报价延迟最少十五分钟。沽空资料截至 2025-04-11 16:25。)AASTOCKS新闻","market":"fut","thumbnail":"https://plib.aastocks.com/aafnnews/image/medialib/20230531121547900_s.jpg","type":0,"news_type":0,"thumbnails":["https://plib.aastocks.com/aafnnews/image/medialib/20230531121547900_s.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.aastocks.com/tc/stocks/news/aafn-con/NOW.1433434/latest-news/AAFN","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":"aastocks_highlight","symbols":["BK1583","LU0501845795.SGD","LU1951186391.HKD","LU0067412154.USD","01093","BK1521","SG9999004220.SGD","BK1576","IE00BZ08YR35.GBP","LU1226287529.USD","BK1515","IE00B543WZ88.USD","IE00BZ08YT58.USD","LU1807302812.USD","LU0140636845.USD","LU1226288170.HKD","BK1191","BK1141","IE00B5MMRT66.SGD","LU1960683339.HKD","LU1008478684.HKD","03347","LU1152091168.USD","LU0072913022.USD","LU1226287792.SGD","IE0008369823.USD","LU1993786604.SGD","IE0008368742.USD","LU1226288253.USD","LU1226287875.USD","IE00B031HY20.USD","LU1152091754.HKD","IE00BZ08YS42.EUR","LU0880133367.SGD","LU0326950275.SGD"],"gpt_icon":0},{"id":"2527957927","title":"恒瑞医药(600276.SH)：注射用HRS-9190获得药物临床试验批准通知书","url":"https://stock-news.laohu8.com/highlight/detail?id=2527957927","media":"智通财经网","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527957927?lang=zh_cn&edition=fundamental","pubTime":"2025-04-13 17:11","pubTimestamp":1744535514,"startTime":"0","endTime":"0","summary":"智通财经APP讯，恒瑞医药 发布公告，近日，公司收到国家药品监督管理局核准签发关于注射用HRS-9190的《药物临床试验批准通知书》，将于近期开展临床试验，同意本品开展“用于全身麻醉诱导期气管插管及维持术中骨骼肌松弛”的临床试验。注射用HRS-9190为术中用药的1类新药，用于全身麻醉诱导期气管插管及维持术中骨骼肌松弛。截至目前，注射用HRS-9190相关项目累计研发投入约626万元。","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/1277822.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":"highlight_zhitongcaijin","symbols":["BK0196","BK1576","LU2488822045.USD","LU1969619763.USD","03347","600276","BK0028","BK0188","LU1064130708.USD","BK0060","BK1141","LU1328615791.USD","BK1583","BK0239","LU0405327494.USD","LU0405327148.USD","BK0012","BK0183","LU2328871848.SGD","LU2148510915.USD","LU1064131003.USD"],"gpt_icon":0},{"id":"2527579929","title":"恒瑞医药(600276.SH)：SHR-3792注射液获批开展晚期实体瘤的临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2527579929","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527579929?lang=zh_cn&edition=fundamental","pubTime":"2025-04-13 17:09","pubTimestamp":1744535355,"startTime":"0","endTime":"0","summary":"智通财经APP讯，恒瑞医药(600276.SH)发布公告，近日，公司子公司上海恒瑞医药有限公司、苏州盛迪亚生物医药有限公司收到国家药品监督管理局(简称“国家药监局”)核准签发关于SHR-3792注射液的《药物临床试验批准通知书》，将于近期开展临床试验，同意本品开展晚期实体瘤的临床试验。SHR-3792注射液是公司自主研发的创新型抗肿瘤候选药物，在临床前动物模型中展现了良好的抗肿瘤活性。经查询，目前国内外尚无同类药物获批上市。截至目前，SHR-3792注射液相关项目累计研发投入约3,271万元。","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/1277819.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":["BK0188","BK0012","LU1328615791.USD","LU1969619763.USD","LU0405327148.USD","BK1576","LU2328871848.SGD","BK0196","BK1141","LU1064131003.USD","BK1583","BK0028","BK0239","600276","BK0183","LU1064130708.USD","LU2148510915.USD","BK0060","LU0405327494.USD","LU2488822045.USD","03347"],"gpt_icon":0},{"id":"2526168654","title":"兆科眼科-B：BRIMOCHOLPF第II期临床试验入组首名患者","url":"https://stock-news.laohu8.com/highlight/detail?id=2526168654","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2526168654?lang=zh_cn&edition=fundamental","pubTime":"2025-04-11 18:29","pubTimestamp":1744367340,"startTime":"0","endTime":"0","summary":"兆科眼科-B发布公告，BRIMOCHOLPF(公司候选药物之一，适...兆科眼科-B(06622)发布公告，BRIMOCHOLPF(公司候选药物之一，适应症为老花眼)的第II期临床试验已于2025年3月24日入组首名患者。该试验的主要目的为评估BRIMOCHOLPF滴眼液对中国老花眼患者的疗效及安全性。根据协议条款，公司有权授予Lunatus于沙特阿拉伯王国、阿拉伯联合酋长国、科威特、阿曼、巴林及卡塔尔进口、分销、推广、营销及销售BRIMOCHOLPF的独家权利。","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=nesSN20250411183200a4560adc&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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