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泰格医药
26.750
+0.900
3.48%
手动刷新
成交量:
185.02万
成交额:
4,912.00万
市值:
231.37亿
市盈率:
53.41
高:
26.950
开:
26.100
低:
26.000
收:
25.850
数据加载中...
总览
公司
新闻
公告
君圣泰医药-B:熊去氧胆小檗硷(HTD1801)在2型糖尿病患者中开展的两项3期临床试验达到主要终点
格隆汇
·
04-15
君圣泰医药-B(02511)宣布熊去氧胆小檗硷(HTD1801)在2型糖尿病患者中开展的两项3期临床试验达到主要终点
智通财经
·
04-15
金十数据整理:每日美股市场要闻速递(4月14日,周一)
美港电讯
·
04-14
新诺威:控股子公司SYS6041抗体偶联药物获得美国药物临床试验批准
美港电讯
·
04-14
石药集团(01093):SYS 6041(抗体偶联药物)获美国临床试验批准
智通财经
·
04-14
国药集团中国生物首款带状疱疹mRNA疫苗获批临床
美港电讯
·
04-14
万泰生物:九价HPV疫苗启动男性III期临床试验并完成首例受试者入组
美港电讯
·
04-14
新诺威(300765.SZ)控股子公司SYS6041抗体偶联药物获得美国药物临床试验批准
智通财经
·
04-14
【新诺威:控股子公司SYS6041抗体偶联药物获得美国药物临床试验批准】金融界4月14日消息,新诺威控股子公司石药集团巨石生物制药有限公司申报的注射用SYS6041药品临床试验申请已获得美国FDA批准,可以在美国开展针对晚期实体瘤的临床试验。该药物是一款单克隆抗体偶联药物,此前已于2025年1月获得中国国家药品监督管理局批准开展临床试验。药物获得临床试验批准后,尚需开展一系列临床试验并经美国FDA批准方可上市、销售,且药物研发具有高投入、高风险、周期长等特点,短期对巨石生物及公司业绩不会产生重大影响。
金融界
·
04-14
【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。
金融界
·
04-14
泰格医药04月14日获主力加仓323万元
市场透视
·
04-14
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
·
04-14
恒瑞医药(600276.SH):SHR-1819注射液获得药物临床试验批准通知书
格隆汇
·
04-14
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
·
04-14
恒瑞医药(600276.SH):获得药物临床试验批准通知书
格隆汇
·
04-14
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
智通财经
·
04-14
【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。
金融界
·
04-14
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
·
04-14
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
·
04-14
石药集团(01093.HK)SYH2046片获准开展临床试验
阿斯达克财经
·
04-13
更多
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08:07","pubTimestamp":1744675655,"startTime":"0","endTime":"0","summary":"格隆汇4月15日丨君圣泰医药-B发布公告,公司自主研发的肠肝抗炎及代谢调节剂熊去氧胆小檗硷在中国2型糖尿病患者中开展的两项3期临床试验达成主要疗效终点及多个次要疗效终点。这两项3期临床试验结果充分证明了HTD1801一药多效、为T2DM患者提供综合获益的特性。基于此次发布的积极的临床试验数据,君圣泰医药计划于今年内向国家药品监督管理局药品审评中心递交HTD1801治疗T2DM适应症的新药上市申请。","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=nesSN20250415080735a4590bf4&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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21:00","pubTimestamp":1744635658,"startTime":"0","endTime":"0","summary":null,"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://www.ushknews.com/","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":"live_meigang","symbols":["03347","LU1917777945.USD","LU0528227936.USD","X","LU0323591593.USD","LU2247934214.USD","LU1064131342.USD","PFE","BK4077","IE00B7KXQ091.USD","LU1206712785.SGD","LU2077746001.SGD","BK4599","LLY","LU0795875169.SGD","LU0784385840.USD","LU0354030511.USD","IE00B19Z8W00.USD","CHA","IE00BJJMRX11.SGD","LU1496350502.SGD","AAPL","LU0314106906.USD","LU2237443549.SGD","LU1582987597.SGD","LU0314104364.USD","LU1861559042.SGD","LU1670710588.SGD","LU1668664300.SGD","LU2602419157.SGD","LU1564329115.USD","LU0109391861.USD","LU1989764664.SGD","LU0823421333.USD","BK4504","SONY","LU2065171402.SGD","LU1989772923.USD","INTC","LU2237438978.USD","MACW.SI","LU0820562030.AUD","LU1267930490.SGD","LU0079474960.USD","LU1316542783.SGD","FTC","IE00BKDWB100.SGD","BK4592","LU1935042215.USD","META"],"gpt_icon":1},{"id":"2527513726","title":"新诺威:控股子公司SYS6041抗体偶联药物获得美国药物临床试验批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2527513726","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527513726?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 18:46","pubTimestamp":1744627561,"startTime":"0","endTime":"0","summary":null,"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://www.ushknews.com/","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":"live_meigang","symbols":["03347","BK1576","BK1583","BK1141","300765","BK0226"],"gpt_icon":0},{"id":"2527138162","title":"石药集团(01093):SYS 6041(抗体偶联药物)获美国临床试验批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2527138162","media":"智通财经","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527138162?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 17:50","pubTimestamp":1744624248,"startTime":"0","endTime":"0","summary":"智通财经APP讯,石药集团(01093)发布公告,集团开发的SYS 6041( 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":"国药集团中国生物首款带状疱疹mRNA疫苗获批临床","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_cn&edition=fundamental","pubTime":"2025-04-14 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16:49","pubTimestamp":1744620548,"startTime":"0","endTime":"0","summary":"智通财经APP讯,新诺威(300765.SZ)公告,公司的控股子公司石药集团巨石生物制药有限公司(简称“巨石生物”)于近日收到美国食品药品监督管理局(简称“FDA”)通知,由巨石生物申报的注射用SYS6041药品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。据悉,SYS6041是一款单克隆抗体偶联药物,可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。本次获批临床的适应症为晚期实体瘤。","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/1278138.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":["BK0226","BK1583","03347","300765","BK1576","BK1141"],"gpt_icon":0},{"id":"2527618188","title":"【新诺威:控股子公司SYS6041抗体偶联药物获得美国药物临床试验批准】金融界4月14日消息,新诺威控股子公司石药集团巨石生物制药有限公司申报的注射用SYS6041药品临床试验申请已获得美国FDA批准,可以在美国开展针对晚期实体瘤的临床试验。该药物是一款单克隆抗体偶联药物,此前已于2025年1月获得中国国家药品监督管理局批准开展临床试验。药物获得临床试验批准后,尚需开展一系列临床试验并经美国FDA批准方可上市、销售,且药物研发具有高投入、高风险、周期长等特点,短期对巨石生物及公司业绩不会产生重大影响。","url":"https://stock-news.laohu8.com/highlight/detail?id=2527618188","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527618188?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 16:44","pubTimestamp":1744620289,"startTime":"0","endTime":"0","summary":"金融界4月14日消息,新诺威控股子公司石药集团巨石生物制药有限公司申报的注射用SYS6041药品临床试验申请已获得美国FDA批准,可以在美国开展针对晚期实体瘤的临床试验。该药物是一款单克隆抗体偶联药物,此前已于2025年1月获得中国国家药品监督管理局批准开展临床试验。药物获得临床试验批准后,尚需开展一系列临床试验并经美国FDA批准方可上市、销售,且药物研发具有高投入、高风险、周期长等特点,短期对巨石生物及公司业绩不会产生重大影响。","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://24h.jrj.com.cn/2025/04/14164449520123.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":["IE00BZ08YT58.USD","BK1576","LU0072913022.USD","LU0501845795.SGD","LU1226287875.USD","01093","300765","SG9999004220.SGD","LU1951186391.HKD","LU1226288253.USD","IE0008368742.USD","IE00B543WZ88.USD","IE00B5MMRT66.SGD","LU1226287792.SGD","LU1960683339.HKD","IE0008369823.USD","BK1141","BK1515","IE00BZ08YR35.GBP","IE00BZ08YS42.EUR","LU0140636845.USD","LU1008478684.HKD","IE00B031HY20.USD","BK0226","LU1226288170.HKD","LU0880133367.SGD","BK1583","LU0067412154.USD","BK1521","LU1152091168.USD","LU0326950275.SGD","LU1226287529.USD","03347","LU1807302812.USD","LU1152091754.HKD","BK1191","LU1993786604.SGD"],"gpt_icon":0},{"id":"2527818864","title":"【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。","url":"https://stock-news.laohu8.com/highlight/detail?id=2527818864","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527818864?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 16:43","pubTimestamp":1744620189,"startTime":"0","endTime":"0","summary":"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。","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/2025/04/14164349520116.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":["03347","BK0226","300765","BK1583","BK1141","BK1576"],"gpt_icon":0},{"id":"2527861491","title":"泰格医药04月14日获主力加仓323万元","url":"https://stock-news.laohu8.com/highlight/detail?id=2527861491","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527861491?lang=zh_cn&edition=fundamental","pubTime":"2025-04-14 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 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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":["BK1576","BK1141","BK0239","BK1583","BK0070","03347","BK0188","002262"],"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 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