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泰格医药

51.100

+0.6501.29%

成交量：559.00万

成交额：2.87亿

市值：439.97亿

市盈率：99.62

高：52.500

开：51.800

低：50.400

收：50.450

数据加载中...

总览公司新闻公告

【港股异动 | 云顶新耀(01952.HK)涨超4% 宣布EVER001治疗原发性膜性肾病临床试验数据取得积极结果】智通

盘前公告淘金：微芯生物临床试验获FDA受理、华菱线缆中标4.56亿电力新能源项目，千里科技6月新能源车销量增长74.11%

加科思-B(01167)完成泛KRAS抑制剂JAB-23E73 I/IIa期临床试验在美国的首例患者给药

【加科思-B(01167.HK)完成泛KRAS抑制剂JAB-23E73 I/IIa期临床试验在美国的首例患者给药】智通财

【美股异动 | 医药板块逆市走高 Moderna(MRNA.US)涨超1.6%】智通财经APP获悉，周二，美股医药板块逆

云顶新耀宣布治疗原发性膜性肾病的新型BTK抑制剂EVER001在1b/2a期临床试验最新阶段性数据，持续展现优异的有效性与安全性

7月1日界面新闻记者获悉赛诺菲将对天演药业进行战略投资并启动双方SAFEbody安全抗体合作框架下的第三个SAFEbod

微芯生物：CS231295临床试验申请获FDA受理

【微芯生物：CS231295临床试验申请获FDA受理】微芯生物公告，公司全资子公司微芯生物科技（美国）有限公司于2025年6月30日收到美国食品药品监督管理局（FDA）的书面回复，自主研发的CS231295关于晚期实体瘤的临床试验申请获得FDA受理。受理号为IND176942，受理日期为2025年6月30日，适应症为晚期实体瘤，申请事项为新药临床试验申请。CS231295作为透脑AuroraB选择性抑制剂，目前全球尚无同类设计的药物进入临床试验阶段。

昂利康：目前在研的创新药项目仅有一个

海正药业：收到HS387片临床试验批准通知书

安科生物：公司AK2024注射液获得药物临床试验批准

安科生物(300009.SZ)：AK2024注射液临床试验获批准

安科生物：AK2024注射液获药物临床试验批准

两部门：探索为创新药研发提供必要的医保数据服务

国家医保局

慧与涨12.6%瞻博网络涨8.4%司法部已就其对慧与以 140 亿美元收购瞻博网络的诉讼达成和解。Moderna涨3.3

【华东医药：全资子公司获得美国FDA新药临床试验批准通知】华东医药6月30日公告，全资子公司杭州中美华东制药有限公司收到美国食品药品监督管理局通知，由中美华东申报的注射用HDM2012药品临床试验申请已获得美国FDA批准，可在美国开展I期临床试验，适应症为晚期实体瘤。

【兴证全球基金增持泰格医药(03347.HK)30.03万股每股作价约35.66港元】智通财经APP获悉，香港联交所最

【康弘药业：子公司收到KH813注射液临床试验批准通知书】康弘药业(002773.SZ)公告称，公司全资子公司成都康弘生物科技有限公司收到国家药品监督管理局签发的《药物临床试验批准通知书》，同意KH813注射液按生物类似药开展临床试验。KH813注射液是康弘生物研发的帕博利珠单抗生物类似药，主要用于治疗多种晚期实体瘤。由于药品研发存在不确定性，投资者需谨慎决策并注意投资风险。

【Moderna美股盘前涨超6%】Moderna美股盘前涨超6%，此前公司宣布实验性流感疫苗达到三期临床试验主要终点。

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