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泰格医药

26.550

-0.200-0.75%

成交量：96.74万

成交额：2,567.27万

市值：229.64亿

市盈率：53.10

高：26.950

开：26.550

低：26.150

收：26.750

数据加载中...

总览公司新闻公告

【石药集团(01093.HK)：JMT203(抗GFRAL单克隆抗体)获美国临床试验批准】石药集团(01093.HK)发布公告，公司附属公司上海津曼特生物科技有限公司自主研发的抗体药物JMT203已获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。此前，该产品已经于2023年6月获得中国国家药品监督管理局批准，并正在中国开展临床试验。

石药集团(01093)：JMT203(抗GFRAL单克隆抗体)获美国临床试验批准

科伦博泰生物-B现涨超4% 创新ADC药物SKB518新药临床试验申请获FDA批准

医药外包概念全线飘红药明生物(02269)涨超3% 机构指板块存在超跌机会 FDA新政下AI制药价值凸显

中欧基金葛兰：看好创新药、消费医疗、医疗设备等板块投资机遇

港股异动 | 先声药业(02096)现涨超8% SIM0686获准开展临床试验后续多款新药获批在望

奥辰生物（云南）有限公司药品申请临床试验默示许可获受理

吉利德科学(GILD.O)宣布Trodelvy（戈沙妥珠单抗）联合Keytruda（帕博利珠单抗）在第三级临床试验中达到

科伦药业：子公司SKB518新药临床试验申请获FDA批准

科伦博泰生物-B(06990)：创新ADC药物SKB518新药临床试验申请获美国食品药品监督管理局批准

恒瑞医药：子公司收到药物临床试验批准通知书

【百奥泰：注射用BAT7111获药物临床试验批准】百奥泰公告，公司于近日收到国家药监局核准签发的《药物临床试验批准通知书》，公司在研药品注射用BAT7111用于晚期实体瘤的临床试验申请获得批准。根据《Clinical Development Success Rates2011-2020》公布的数据，通常情况下对于抗肿瘤药物，一般I/II期临床研究阶段持续约2年时间，I期完成进入II期的比率约48.8%，II期完成进入III期的比率约24.6%。考虑到临床研究周期长、投入大，过程中不可预测因素较多，临床试验、审评和审批的结果以及时间都具有一定的不确定性。

中国人民银行等四部门：加大对出口企业的保险支持力度

晚期实体瘤药物喜讯不断，人福医药、汇宇制药、翰森制药等多药企获批临床试验

【改善患者肢体运动功能 “植入式迷走神经刺激系统”临床试验启动】今天，国家卫生健康委组织实施的“百万减残”工程重点推广项目，我国自主研发的“植入式迷走神经刺激系统”临床试验正式全国启动。该项目有望成为我国卒中后残疾防控的重要手段。

Sands Capital Management,LP减持泰格医药(03347)38.41万股每股作价为25.9329港元

【沃森生物：20价肺炎球菌多糖结合疫苗获临床试验批准】沃森生物公告，公司及子公司共同申请的20价肺炎球菌多糖结合疫苗获得国家药品监督管理局签发的《药物临床试验批准通知书》，通知书编号为2025LP01099。该疫苗是在已上市产品13价肺炎球菌多糖结合疫苗基础上开发的迭代升级产品，新增了8型、10A型、11A型、12F型、15B型、22F型和33F型共计7种血清型，用于预防由本品所含20种肺炎球菌血清型引起的感染性疾病。全球已上市20价肺炎球菌多糖结合疫苗的厂家仅有美国辉瑞公司一家，国内尚未有20价肺炎球菌多糖结合疫苗上市销售。

盛禾（中国）生物制药有限公司药品申请临床试验默示许可获受理

石药集团欧意药业有限公司药品申请临床试验默示许可获受理

普方生物制药（苏州）有限公司药品申请临床试验默示许可获受理

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