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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：51.52

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

翰森制药(03692)：HS-10529片获国家药品监督管理局签发的药物临床试验批准通知书

百诚医药：公司已获得1个1类创新药 10个2类创新药的临床试验批准

中恒集团(600252.SH)全资子公司获药物临床试验批准通知书

智通财经网

百利天恒(688506.SH)：注射用BL-B01D1联合用药治疗多种晚期实体瘤获批II期临床试验

【百利天恒：BL-B01D1（EGFR×HER3 双抗 ADC）联合用药治疗多种晚期实体瘤获 4 个 II 期药物临床试验批准通知书】金融界4月15日消息，百利天恒近日收到国家药品监督管理局正式批准签发的 4 个《药物临床试验批准通知书》，公司自主研发的创新生物药注射用 BL-B01D1（EGFR×HER3 双抗 ADC）的 4 个联合用药的 II 期临床试验获得批准。注射用 BL-B01D1 临床试验符合药品注册要求，同意开展联合仑伐替尼用于晚期肝癌、联合阿昔替尼±帕博利珠单抗用于晚期肾癌、联合贝伐珠单抗±化疗用于晚期结直肠癌、联合帕博利珠单抗±化疗用于晚期胆道恶性肿瘤的临床试验。BL-B01D1 是全球首创且唯一进入 III 期临床阶段的 EGFR×HER3 双抗 ADC，除本次新批准的 4 项临床试验外，正在中国和美国进行 30 余项针对十余种肿瘤类型的临床试验。药品需完成相关临床试验并通过审评、审批后方可上市销售，医药产品具有诸多特点，从研究到投产环节多，易受不确定性因素影响。

Dupixent专利到期后恐陷“青黄不接” 赛诺菲(SNY.US)下一代哮喘药临床试验结果不佳

港股生物医药板块持续走弱，泰格医药跌超4%

每日经济新闻

港股生物医药板块持续走弱，泰格医药(03347.HK)跌超4%，百济神州(06160.HK)跌超2%，药明康德(0235

泰格医药盘中异动早盘急速下跌5.18%

港股异动 | 君圣泰医药-B(02511)涨超14% 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

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

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

金十数据整理：每日美股市场要闻速递（4月14日，周一）

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

石药集团(01093)：SYS 6041(抗体偶联药物)获美国临床试验批准

国药集团中国生物首款带状疱疹mRNA疫苗获批临床

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

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

【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。

【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。

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双抗 ADC）联合用药治疗多种晚期实体瘤获 4 个 II 期药物临床试验批准通知书】金融界4月15日消息，百利天恒近日收到国家药品监督管理局正式批准签发的 4 个《药物临床试验批准通知书》，公司自主研发的创新生物药注射用 BL-B01D1（EGFR×HER3 双抗 ADC）的 4 个联合用药的 II 期临床试验获得批准。注射用 BL-B01D1 临床试验符合药品注册要求，同意开展联合仑伐替尼用于晚期肝癌、联合阿昔替尼±帕博利珠单抗用于晚期肾癌、联合贝伐珠单抗±化疗用于晚期结直肠癌、联合帕博利珠单抗±化疗用于晚期胆道恶性肿瘤的临床试验。BL-B01D1 是全球首创且唯一进入 III 期临床阶段的 EGFR×HER3 双抗 ADC，除本次新批准的 4 项临床试验外，正在中国和美国进行 30 余项针对十余种肿瘤类型的临床试验。药品需完成相关临床试验并通过审评、审批后方可上市销售，医药产品具有诸多特点，从研究到投产环节多，易受不确定性因素影响。","url":"https://stock-news.laohu8.com/highlight/detail?id=2527464947","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527464947?lang=zh_cn&edition=fundamental","pubTime":"2025-04-15 17:25","pubTimestamp":1744709155,"startTime":"0","endTime":"0","summary":"金融界4月15日消息，百利天恒近日收到国家药品监督管理局正式批准签发的 4 个《药物临床试验批准通知书》，公司自主研发的创新生物药注射用 BL-B01D1 的 4 个联合用药的 II 期临床试验获得批准。BL-B01D1 是全球首创且唯一进入 III 期临床阶段的 EGFR×HER3 双抗 ADC，除本次新批准的 4 项临床试验外，正在中国和美国进行 30 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赛诺菲(SNY.US)下一代哮喘药临床试验结果不佳","url":"https://stock-news.laohu8.com/highlight/detail?id=2527662894","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527662894?lang=zh_cn&edition=fundamental","pubTime":"2025-04-15 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