美股详情

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Provident Financial Services Inc

16.64

+0.11000.67%

成交量：53.87万

成交额：894.88万

市值：21.74亿

市盈率：14.01

高：16.70

开：16.45

低：16.40

收：16.53

数据加载中...

总览公司新闻公告

【华东医药：独家市场推广产品塞纳帕利胶囊获批上市】华东医药公告，公司全资子公司杭州中美华东制药有限公司独家市场推广产品塞纳帕利胶囊（商品名：派舒宁，研发代号：IMP4297）获得国家药品监督管理局批准上市，用于晚期上皮性卵巢癌、输卵管癌或原发性腹膜癌成人患者在一线含铂化疗达到完全缓解或部分缓解后的维持治疗。塞纳帕利胶囊的获批是基于FLAMES研究，该研究结果显示，塞纳帕利维持治疗能够显著延长晚期卵巢癌患者的无进展生存期（PFS），且不论患者的BRCA基因表达如何，均能从塞纳帕利治疗中获益。同时，塞纳帕利耐受性良好，安全性可控。

信达生物与奥赛康药业宣布第三代EGFR TKI 肺癌靶向药物奥壹新®（利厄替尼片）获批上市

恒瑞正式递表港交所，开启国际化的第二步

华尔街见闻

中国国家药品监督管理局批准威络益（佐妥昔单抗）一线治疗晚期胃或胃食管交界处腺癌

信达生物宣布ROS1抑制剂达伯乐®（己二酸他雷替尼胶囊）获批第二项适应症，用于全线治疗 ROS1 阳性肺癌

泰瑞沙®在中国获批治疗EGFR突变Ⅲ期不可切除非小细胞肺癌

【中国生物制药(01177.HK)：贝莫苏拜单抗注射液联合化疗后序贯联合盐酸安罗替尼胶囊对比替雷利珠单抗注射液联合化疗用于晚期鳞状非小细胞肺癌一线治疗III期研究取得阳性结果】中国生物制药(01177.HK)发布公告，集团自主研发的1类创新药贝莫苏拜单抗注射液联合化疗后序贯联合盐酸安罗替尼胶囊对比替雷利珠单抗注射液联合化疗用于晚期鳞状非小细胞肺癌(sq-NSCLC)一线治疗的III期研究(TQB2450-III-12)已完成方案预设的期中分析，独立数据监查委员会(IDMC)判定主要研究终点无进展生存期(PFS)达到方案预设的优效界值。本集团已与中国国家药品监督管理局(NMPA)药品审评中心(CDE)就该适应症的上市申请进行沟通，并获得CDE书面同意提交贝莫苏拜单抗注射液、盐酸安罗替尼胶囊新增该一线适应症的上市申请。本集团将于近期递交上市申请。

肿瘤药竞赛，上了新高度

【湾区早参】香港推动黄金市场发展工作小组正式成立；深圳每年发放最高5亿元“训力券”

公积金金融服务盘中异动快速下挫5.00%报19.18美元

吉利德肿瘤药卖不动了？新药失利、裁员调整

医药经济报

一周内官宣4笔BD交易！双抗新药赛道火爆，跨国药企砸百亿在华“扫货”

特朗普任内预计地区银行股将大放异彩！华尔街对这7只高股息相关股青睐有加

老虎资讯综合

公积金金融服务盘中异动早盘股价大涨12.18%报21.36美元

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T790M突变阳性的局部晚期或转移性非小细胞肺癌成人患者治疗。","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://wwwold.prnasia.com/story/archive/4598259_ZH98259_1","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":"prnasia","symbols":["PFS","BK4139","LU2488822045.USD","BK4211","BK4195","PPI","IVBIY","ORR","01801","BK1583","LU2328871848.SGD","BK4570","BK1589","BK1161","LU1969619763.USD"],"gpt_icon":0},{"id":"2501721910","title":"恒瑞正式递表港交所，开启国际化的第二步","url":"https://stock-news.laohu8.com/highlight/detail?id=2501721910","media":"华尔街见闻","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2501721910?lang=zh_cn&edition=fundamental","pubTime":"2025-01-07 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20:18","pubTimestamp":1735820280,"startTime":"0","endTime":"0","summary":"中国患者的临床获益和全球患者一致：接受奥希替尼治疗组12个月和24个月的PFS率分别为80%、71%，而安慰剂组仅为17%和8%[4]。Ⅲ期肺癌分为可切除、潜在切除和不可切除三大类，其中不可切除的Ⅲ期非小细胞肺癌患者占大多数[6]，病程进展最为严峻。非常高兴看到奥希替尼治疗EGFR突变Ⅲ期不可切除肺癌的适应症在中国获批，填补了几十年来的临床空白，这对不可切除的EGFR突变Ⅲ期肺癌患者来说是一个重大突破，为他们带来长生存的希望。","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://wwwold.prnasia.com/story/archive/4587876_ZH87876_1","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":"prnasia","symbols":["LU2456880835.USD","LU2417539215.USD","BK4135","OS","BK4211","PFS","LU0109394709.USD","BK4568","CNS","LU2462157665.USD","CDE","BK4195","LU1829250122.USD","BK4585","BK4017","LU0889565916.HKD","BK4007","LU0320765992.SGD","CRT","BK4097","LU2236285917.USD","BK4588","BK4213","AZN"],"gpt_icon":0},{"id":"2494815465","title":"【中国生物制药(01177.HK)：贝莫苏拜单抗注射液联合化疗后序贯联合盐酸安罗替尼胶囊对比替雷利珠单抗注射液联合化疗用于晚期鳞状非小细胞肺癌一线治疗III期研究取得阳性结果】中国生物制药(01177.HK)发布公告，集团自主研发的1类创新药贝莫苏拜单抗注射液联合化疗后序贯联合盐酸安罗替尼胶囊对比替雷利珠单抗注射液联合化疗用于晚期鳞状非小细胞肺癌(sq-NSCLC)一线治疗的III期研究(TQB2450-III-12)已完成方案预设的期中分析，独立数据监查委员会(IDMC)判定主要研究终点无进展生存期(PFS)达到方案预设的优效界值。本集团已与中国国家药品监督管理局(NMPA)药品审评中心(CDE)就该适应症的上市申请进行沟通，并获得CDE书面同意提交贝莫苏拜单抗注射液、盐酸安罗替尼胶囊新增该一线适应症的上市申请。本集团将于近期递交上市申请。","url":"https://stock-news.laohu8.com/highlight/detail?id=2494815465","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2494815465?lang=zh_cn&edition=fundamental","pubTime":"2024-12-27 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快速下挫5.00%报19.18美元","url":"https://stock-news.laohu8.com/highlight/detail?id=2492315182","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2492315182?lang=zh_cn&edition=fundamental","pubTime":"2024-12-19 04:37","pubTimestamp":1734554252,"startTime":"0","endTime":"0","summary":"北京时间2024年12月19日04时37分，公积金金融服务股票出现波动，股价急速下跌5.00%。截至发稿，该股报19.18美元/股，成交量36.6354万股，换手率0.28%，振幅5.89%。公积金金融服务股票所在的银行行业中，整体跌幅为1.65%。该公司的业务仅限于金融服务行业，包括向客户提供传统银行和其他金融服务。该公司有一个单一报告部门用于财务报告目的。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20241219043732984cb88a&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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ADC药物Trodelvy。这一决定无疑对吉利德在肿瘤领域的战略布局产生了深远影响。近日，吉利德披露了一系列裁员计划，这一举措被业内视为其在当前困境下的无奈之举。总的来看，吉利德的新药失利与裁员计划是当前生物制药领域竞争激烈和市场变化的真实写照。近日，吉利德宣布了一项重大裁员计划，引发业界广泛关注。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20241120195516abd1e427&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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