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Provident Financial Services Inc

21.19

+1.336.70%

盘后：21.190.00000.00%18:09 EST

成交量：144.00万

成交额：3,010.44万

市值：27.68亿

市盈率：10.80

高：21.20

开：20.03

低：19.94

收：19.86

52周最高：21.29

52周最低：14.34

股本：1.31亿

流通股本：1.26亿

量比：1.71

换手率：1.14%

股息：0.96

股息率：4.53%

每股收益(TTM):1.96

每股收益(LYR):1.05

净资产收益率：9.51%

总资产收益率：1.05%

市净率：1.00

市盈率(LYR):20.12

数据加载中...

总览公司新闻资讯公告

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Rybrevant双靶风暴来袭：强生重塑难治性结直肠癌治疗天花板，51% ORR+11.3月肝转移PFS，EGFR/MET双锁+免疫杀伤直击耐药痛点

医道社创新药新...

普罗维登特银行年度经济展望调查：企业主从2025年被动乐观转向2026年主动投资

全球首个HER2突变肺癌口服靶向药上新，境外新药加速入华新政助力药品一年落地

肺癌一线！“伏美替尼”新适应症拟纳入突破性疗法

优赫得®在华获批为首个用于既往在转移性疾病阶段经一种或一种以上内分泌治疗进展的HER2低表达或超低表达乳腺癌患者的HER2靶向疗法

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【券商聚焦】交银国际维持康方生物(09926)买入评级指依沃西较PD-1显著提升一线肺鳞癌PFS

这个转移性三阴性乳腺癌一线疗法，相比化疗使疾病进展或死亡风险降低 38%

Provident Bank加强零售业务领导团队，任命Renee Altomonte为执行副总裁兼零售银行总监

韩国生物制药公司Celltrion眼科治疗生物仿制药在美国获批

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第一三共公布TROPION-Breast02 Ⅲ期研究积极的主要结果

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成人患者的治疗。","market":"fut","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/relnews/cn/2025-12-26/doc-inhecrxf2583740.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":["BK4195","ORR","PFS","BK4211"],"gpt_icon":0},{"id":"2594360732","title":"优赫得®在华获批为首个用于既往在转移性疾病阶段经一种或一种以上内分泌治疗进展的HER2低表达或超低表达乳腺癌患者的HER2靶向疗法","url":"https://stock-news.laohu8.com/highlight/detail?id=2594360732","media":"美通社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2594360732?lang=zh_cn&edition=fundamental","pubTime":"2025-12-25 15:30","pubTimestamp":1766647800,"startTime":"0","endTime":"0","summary":"在对HER2超低表达患者进行的探索性分析中，显示HER2超低表达患者群体的试验结果和HER2低表达试验群体的结果具有一致性。经筛查，约85%的HR阳性、HER2阴性转移性乳腺癌患者被检测出有HER2低表达或HER2超低表达3。目前，对于HR阳性转移性乳腺癌患者，不论HER2表达水平如何，内分泌治疗仍被广泛用于早期治疗方案。基于德曲妥珠单抗已取得的临床实践改变，此次获批将为更广泛的HER2表达转移性乳腺癌患者带来亟需的靶向治疗选择。","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://wwwold.prnasia.com/story/archive/4853703_ZH53703_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":["BK4211","BK4588","BK4225","HR","LU0320765992.SGD","LU1829250122.USD","BK4195","BK4585","LU0889565916.HKD","PFS","IHC","BK4231","LU2417539215.USD","BK4568","LU2456880835.USD","ORR","LU0109394709.USD","LU2462157665.USD","ADC","BK4080","AZN","BK4007","BK4203","BK4162","LU2236285917.USD"],"gpt_icon":0},{"id":"2592502964","title":"君赛生物赴港IPO：核心产品数据平平且专利仍待审批 递表前股东要求回购或转让股权","url":"https://stock-news.laohu8.com/highlight/detail?id=2592502964","media":"新浪证券","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2592502964?lang=zh_cn&edition=fundamental","pubTime":"2025-12-17 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23:45","pubTimestamp":1765899900,"startTime":"0","endTime":"0","summary":"FDA批准阿斯利康（AZN）与第一三共（Daiichi Sankyo，TYO：4568）的fam-trastuzumab deruxtecan（Enhertu）联合帕妥珠单抗（pertuzumab）用于一线治疗，因DESTINY-Breast09试验显示其中位无进展生存期（PFS）达40.7个月，优于标准THP方案的26.9个月；帕妥珠单抗由罗氏（SWX：ROG）销售。\n\n\n海量资讯、精准解读，尽在新浪财经APP\n\n责任编辑：张俊 SF065","market":"fut","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/usstock/c/2025-12-16/doc-inhaziff7927164.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":"sina","symbols":["PFS","LU2236285917.USD","BK4568","LU0109394709.USD","LU0320765992.SGD","BK4211","AZN","LU0889565916.HKD","BK4585","LU2456880835.USD","BK4588","LU1829250122.USD","LU2462157665.USD","BK4195","LU2417539215.USD","BK4007"],"gpt_icon":0},{"id":"2590451393","title":"吉利德Anito-cel 神经毒性低，2年多发性骨髓瘤生存率高 | ASH25","url":"https://stock-news.laohu8.com/highlight/detail?id=2590451393","media":"Minhua笔记","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590451393?lang=zh_cn&edition=fundamental","pubTime":"2025-12-08 11:58","pubTimestamp":1765166299,"startTime":"0","endTime":"0","summary":"在ASH 2025年会上，吉利德旗下Kite Pharma公布Anito-cel在iMMagine-1 II期试验中的更新数据，该靶向BCMA的CAR-T疗法在复发/难治性多发性骨髓瘤患者中显示96% ORR、74% sCR/CR率、95% MRD阴性率，中位随访15.9个月，缓解持续。III期iMMagine-3试验正在招募中，该研究将Anito-cel与标准治疗比较，预计2026年获得数据；该药物获FDA快速通道、孤儿药和RMAT资格。ICANS 发生率为 8%，其中 1 例为 3 级；其余均为 2 级或更低。","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=nesSN20251208144817a43ac231&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description 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20:07","pubTimestamp":1764763653,"startTime":"0","endTime":"0","summary":"多伦多，2025年12月3日-- Emerita Resources Corp.很高兴地宣布已将伊比利亚带西部可行性研究的完成合同授予SLR Consulting Limited。Wardell Armstrong在2024年10月被SLR收购，至今一直是负责IBW矿产资源估算的合格评估师，并且在IBW的冶金测试中积极参与。SLR在经过严谨的招标过程后获得了此项工作。初始的二十三家公司经过筛选，缩减至五家公司，并考虑了详细提案。SLR的提案在时机、对IBW项目及该地区其他项目的熟悉程度及整体价值方面提供了最佳契合。PFS预计将在大约六个月内完成。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","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":null,"symbols":["BK4211","BK4168","EMOTF","BK4195","PFS"],"gpt_icon":0},{"id":"2584941686","title":"iza-bren食管鳞癌Ⅲ期临床期中分析迎关键突破","url":"https://stock-news.laohu8.com/highlight/detail?id=2584941686","media":"每日经济新闻","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2584941686?lang=zh_cn&edition=fundamental","pubTime":"2025-11-19 21:09","pubTimestamp":1763557767,"startTime":"0","endTime":"0","summary":"在创新药研发的竞技场上，Ⅲ期临床的“期中大考”是检验药物价值的试金石。11月18日，百利天恒（SH688506，股价369.30元，市值1525.00亿元）宣布其核心产品——全球首创的EGFR×HER3双抗ADC（抗体药物偶联物）药物izabren，在晚期食管鳞癌Ⅲ期临床试验的预设期中分析中，同时达到无进展生存期和总生存期双主要终点。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202511193569015549.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202511193569015549.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_eastmoney","symbols":["PFS","BK4211","02615","BK4097","91194","BK4195","ORR","OS"],"gpt_icon":0},{"id":"2580280025","title":"医药界“泡泡玛特”：递表港交所","url":"https://stock-news.laohu8.com/highlight/detail?id=2580280025","media":"药事纵横","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2580280025?lang=zh_cn&edition=fundamental","pubTime":"2025-11-02 08:02","pubTimestamp":1762041764,"startTime":"0","endTime":"0","summary":"VIS-101已在美国和中国完成了初步的安全性和剂量递增研究，目前正在中国完成一项随机剂量范围的II期研究。VIS-101预计将于2026年具备开展III期试验的条件。此次收购已通过新成立的子公司Visara完成的。“我们要做医药行业的‘泡泡玛特’。”傅唯用一个生动的比喻解释，泡泡玛特的核心是“连接设计师与全球渠道”，新桥要做的是“连接中国创新药研发者与全球市场”。","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=nesSN20251102080748a481f874&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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13:37","pubTimestamp":1761197821,"startTime":"0","endTime":"0","summary":"美银证券发表报告，将科伦博泰生物的目标价由471.5港元上调至522港元，重申“中性”评级。临床进展符合预期，但短期授权机会有限。该行指，为反映sac-TMT与A166在无进展生存期方面取得显著改善的鼓舞性数据，以及近期国家药监局批准sac-TMT用于二线EGFR突变非小细胞肺癌及A166用于二线以上HER2阳性乳腺癌，因此上调目标价，并将2025至2027年营收预测上调1%至5%，并调高长期预测。","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://sc.stock.cnfol.com/gushizhibo/20251023/31730314.shtml","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":"zhongjincaijing_highlight","symbols":["BC","BK4195","BK4211","PFS","BK4190"],"gpt_icon":0},{"id":"2577681314","title":"【券商聚焦】交银国际维持康方生物(09926)买入评级 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