港股詳情

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泰格醫藥

25.850

-0.700-2.64%

成交量：354.76萬

成交額：9,277.14萬

市值：223.59億

市盈率：51.59

高：26.650

開：26.000

低：25.500

收：26.550

資料載入中...

總覽公司新聞公告

【新諾威：SYS6041抗體偶聯藥物獲美國臨牀試驗批准】新諾威公告，控股子公司巨石生物申報的SYS6041注射劑臨牀試驗申請已獲得美國FDA批准，可以在美國開展臨牀試驗。該藥物是一款單克隆抗體偶聯藥物，適用於晚期實體瘤，已在國內外提交多件專利申請。此前，該產品已於2025年1月獲得中國國家藥品監督管理局批准，可以在中國開展臨牀試驗。

泰格醫藥04月14日獲主力加倉323萬元

恆瑞醫藥(600276.SH)子公司多款藥品獲藥物臨牀試驗批准通知書

智通财经网

恆瑞醫藥(600276.SH)：SHR-1819注射液獲得藥物臨牀試驗批准通知書

恆瑞醫藥(600276.SH)SHR-1819注射液獲藥物臨牀試驗批准通知書

智通财经网

恆瑞醫藥(600276.SH)：獲得藥物臨牀試驗批准通知書

恩華藥業(002262.SZ)：NH280105在澳大利亞啓動I期臨牀試驗並完成首例受試者入組和給藥

【恩華藥業：NH280105在澳大利亞啓動I期臨牀試驗並完成首例受試者入組和給藥】恩華藥業公告，公司全資子公司上海樞境生物科技有限公司近日收到澳大利亞人類研究倫理委員會簽發的批准NH280105膠囊開展I期臨牀試驗的臨牀試驗倫理許可，並已向澳大利亞藥品管理局（TGA）進行臨牀試驗備案。NH280105是一種口服高選擇性Lp-PLA2抑制劑，擬用於阿爾茨海默病的治療。該藥物通過抑制Lp-PLA2，減少炎症反應並修復血腦屏障，改善患者的認知功能。本次臨牀試驗為NH280105首次在人類受試者中開展的I期臨牀試驗，旨在評估健康成人受試者單次和多次口服NH280105膠囊的安全性、耐受性和藥代動力學特徵。

港股異動 | 石藥集團(01093)漲超5% SYH2046片獲中國臨牀試驗批准

智通财经网

博雅生物擬掛牌轉讓子公司80%股權；恆瑞醫藥兩款藥物獲批臨牀試驗｜醫藥早參

每日经济新闻

石藥集團(01093.HK)SYH2046片獲準開展臨牀試驗

阿斯达克财经

恆瑞醫藥(600276.SH)：注射用HRS-9190獲得藥物臨牀試驗批准通知書

智通财经网

恆瑞醫藥(600276.SH)：SHR-3792注射液獲批開展晚期實體瘤的臨牀試驗

兆科眼科-B：BRIMOCHOLPF第II期臨牀試驗入組首名患者

石藥集團(01093)：SYH2046片獲中國臨牀試驗批准

兆科眼科(06622.HK)治療老花眼藥物II期臨牀試驗入組首名患者另與Lunatus就藥物訂立分銷協議

阿斯达克财经

常山藥業(300255.SZ)：艾本那肽注射液臨牀試驗申請獲受理

兆科眼科-B(06622)：BRIMOCHOL™PF第II期臨牀試驗入組首名患者

匯宇製藥：注射用HY0001a藥物臨牀試驗申請獲受理

匯宇製藥(688553.SH)：注射用HY0001a獲得藥物臨牀試驗申請受理通知書

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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":"恆瑞醫藥(600276.SH)：SHR-1819注射液獲得藥物臨牀試驗批准通知書","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_tw&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":"恆瑞醫藥(600276.SH)SHR-1819注射液獲藥物臨牀試驗批准通知書","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_tw&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":"恆瑞醫藥(600276.SH)：獲得藥物臨牀試驗批准通知書","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_tw&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":"恩華藥業(002262.SZ)：NH280105在澳大利亞啓動I期臨牀試驗並完成首例受試者入組和給藥","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_tw&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":"【恩華藥業：NH280105在澳大利亞啓動I期臨牀試驗並完成首例受試者入組和給藥】恩華藥業公告，公司全資子公司上海樞境生物科技有限公司近日收到澳大利亞人類研究倫理委員會簽發的批准NH280105膠囊開展I期臨牀試驗的臨牀試驗倫理許可，並已向澳大利亞藥品管理局（TGA）進行臨牀試驗備案。NH280105是一種口服高選擇性Lp-PLA2抑制劑，擬用於阿爾茨海默病的治療。該藥物通過抑制Lp-PLA2，減少炎症反應並修復血腦屏障，改善患者的認知功能。本次臨牀試驗為NH280105首次在人類受試者中開展的I期臨牀試驗，旨在評估健康成人受試者單次和多次口服NH280105膠囊的安全性、耐受性和藥代動力學特徵。","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_tw&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":"港股異動 | 石藥集團(01093)漲超5% SYH2046片獲中國臨牀試驗批准","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_tw&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":"博雅生物擬掛牌轉讓子公司80%股權；恆瑞醫藥兩款藥物獲批臨牀試驗｜醫藥早參","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_tw&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":"石藥集團(01093.HK)SYH2046片獲準開展臨牀試驗","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_tw&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":"hk","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":["IE00B031HY20.USD","LU0140636845.USD","IE00BZ08YT58.USD","SG9999004220.SGD","LU1993786604.SGD","01093","IE0008369823.USD","LU1152091754.HKD","03347","LU1807302812.USD","LU1226287529.USD","LU0326950275.SGD","BK1521","LU1960683339.HKD","LU1226287875.USD","LU0501845795.SGD","BK1141","BK1576","LU0880133367.SGD","LU0072913022.USD","IE00BZ08YS42.EUR","LU1152091168.USD","LU1226287792.SGD","LU1951186391.HKD","IE0008368742.USD","IE00BZ08YR35.GBP","LU1226288170.HKD","LU0067412154.USD","BK1515","IE00B543WZ88.USD","LU1226288253.USD","BK1191","LU1008478684.HKD","BK1583","IE00B5MMRT66.SGD"],"gpt_icon":0},{"id":"2527957927","title":"恆瑞醫藥(600276.SH)：注射用HRS-9190獲得藥物臨牀試驗批准通知書","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_tw&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":"恆瑞醫藥(600276.SH)：SHR-3792注射液獲批開展晚期實體瘤的臨牀試驗","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_tw&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期臨牀試驗入組首名患者","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_tw&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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