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泰格醫藥

26.750

+0.9003.48%

成交量：185.02萬

成交額：4,912.00萬

市值：231.37億

市盈率：53.38

高：26.950

開：26.100

低：26.000

收：25.850

資料載入中...

總覽公司新聞公告

泰格醫藥盤中異動早盤急速下跌5.18%

港股異動 | 君聖泰醫藥-B(02511)漲超14% HTD1801在2型糖尿病患者中開展的兩項3期臨牀試驗達到主要終點

君聖泰醫藥-B：熊去氧膽小檗礆(HTD1801)在2型糖尿病患者中開展的兩項3期臨牀試驗達到主要終點

君聖泰醫藥-B(02511)宣佈熊去氧膽小檗礆(HTD1801)在2型糖尿病患者中開展的兩項3期臨牀試驗達到主要終點

金十數據整理：每日美股市場要聞速遞（4月14日，週一）

新諾威：控股子公司SYS6041抗體偶聯藥物獲得美國藥物臨牀試驗批准

石藥集團(01093)：SYS 6041(抗體偶聯藥物)獲美國臨牀試驗批准

國藥集團中國生物首款帶狀皰疹mRNA疫苗獲批臨牀

萬泰生物：九價HPV疫苗啓動男性III期臨牀試驗並完成首例受試者入組

新諾威(300765.SZ)控股子公司SYS6041抗體偶聯藥物獲得美國藥物臨牀試驗批准

【新諾威：控股子公司SYS6041抗體偶聯藥物獲得美國藥物臨牀試驗批准】金融界4月14日消息，新諾威控股子公司石藥集團巨石生物製藥有限公司申報的注射用SYS6041藥品臨牀試驗申請已獲得美國FDA批准，可以在美國開展針對晚期實體瘤的臨牀試驗。該藥物是一款單克隆抗體偶聯藥物，此前已於2025年1月獲得中國國家藥品監督管理局批准開展臨牀試驗。藥物獲得臨牀試驗批准後，尚需開展一系列臨牀試驗並經美國FDA批准方可上市、銷售，且藥物研發具有高投入、高風險、週期長等特點，短期對巨石生物及公司業績不會產生重大影響。

【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

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早盤急速下跌5.18%","url":"https://stock-news.laohu8.com/highlight/detail?id=2527748589","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527748589?lang=zh_tw&edition=fundamental","pubTime":"2025-04-15 11:21","pubTimestamp":1744687279,"startTime":"0","endTime":"0","summary":"2025年04月15日早盘11时21分，泰格医药股票出现异动，股价急速下跌5.18%。截至发稿，该股报25.650港元/股，成交量197.07万股，换手率1.60%，振幅5.36%。资金方面，该股资金流入2376.78万港元，流出1997.84万港元。机构评级方面，在所有14家参与评级的机构中，64%的券商给予买入建议，21%的券商给予持有建议，15%的券商给予卖出建议。泰格医药股票所在的生物技术行业中，整体涨幅为0.92%。","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=nesSN20250415112119a4593460&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, 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抗体偶联药物 )的试验性新药(IND)申请已获得美国食品药品监督管理局(FDA)批准，可以在美国开展临床研究。该产品已于2025年1月获得中华人民共和国国家药品监督管理局批准在中国开展临床试验。该产品为一款单克隆抗体偶联药物，与肿瘤表面的特异性受体结合，通过内吞作用进入细胞并释放毒素，达到杀伤肿瘤细胞的作用。本次获批的适应症为晚期实体瘤。临床前研究显示，该产品对多种癌症均有较好的抗肿瘤作用，具有较高的临床开发价值。该产品已在国内外提交多件专利申请。","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/1278203.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":["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":"2527576182","title":"國藥集團中國生物首款帶狀皰疹mRNA疫苗獲批臨牀","url":"https://stock-news.laohu8.com/highlight/detail?id=2527576182","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527576182?lang=zh_tw&edition=fundamental","pubTime":"2025-04-14 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