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JNJ 强生
交易中 12-15 11:39:20 EST
213.92
+2.34
+1.11%
最高
214.38
最低
209.01
成交量
271.98万
今开
210.35
昨收
211.58
日振幅
2.54%
总市值
5,154亿
流通市值
5,144亿
总股本
24.09亿
成交额
5.80亿
换手率
0.11%
流通股本
24.05亿
市净率
--
ROE
--
每股收益
0.00
52周最高
--
52周最低
--
市盈率
--
股息
--
股息收益率
--
ROA
--
分时
五日
日K
周K
月K
数据加载中...
北京优虎网络科技有限公司
资讯
新帖
简况
FDA授予Teclistamab与Daratumumab联合用于复发/难治性多发性骨髓瘤国家优先奖券
美股速递 · 12-15 23:24
FDA授予Teclistamab与Daratumumab联合用于复发/难治性多发性骨髓瘤国家优先奖券
新闻稿：海恩时富任命艾莉森·E·刘易斯为总裁兼首席执行官
投资观察 · 12-15 20:03
新闻稿：海恩时富任命艾莉森·E·刘易斯为总裁兼首席执行官
美国FDA批准Akeega®作为首款针对BRCA2突变的转移性去势敏感性前列腺癌的精准疗法，疾病进展较标准疗法降低54%
美股速递 · 12-13 09:26
美国FDA批准Akeega®作为首款针对BRCA2突变的转移性去势敏感性前列腺癌的精准疗法，疾病进展较标准疗法降低54%
加州陪审团裁定强生公司需支付4000万美元，因未警告消费者婴儿爽身粉致癌风险
美股速递 · 12-13 08:53
加州陪审团裁定强生公司需支付4000万美元，因未警告消费者婴儿爽身粉致癌风险
FDA批准Niraparib和Abiraterone Acetate联合泼尼松用于BRCA2突变的转移性去势敏感性前列腺癌
美股速递 · 12-13 05:20
FDA批准Niraparib和Abiraterone Acetate联合泼尼松用于BRCA2突变的转移性去势敏感性前列腺癌
欧洲药品管理局推荐扩展Arexvy、Aspaveli、Dovprela、Elucirem、Eylea、Nucala、Recarbrio、Simponi、Uplizna、Vueway的适应症
美股速递 · 12-12
欧洲药品管理局推荐扩展Arexvy、Aspaveli、Dovprela、Elucirem、Eylea、Nucala、Recarbrio、Simponi、Uplizna、Vueway的适应症
花旗上调强生目标价至232美元
格隆汇 · 12-12
花旗上调强生目标价至232美元
强生多发性骨髓瘤联合疗法取得“显著”成果
环球市场播报 · 12-10
强生多发性骨髓瘤联合疗法取得“显著”成果
阶段 III Majestec-3 研究的前所未有结果支持 Tecvayli® 联合 Darzalex Faspro® 作为复发/难治性多发性骨髓瘤患者的潜在第二线标准治疗
美股速递 · 12-09
阶段 III Majestec-3 研究的前所未有结果支持 Tecvayli® 联合 Darzalex Faspro® 作为复发/难治性多发性骨髓瘤患者的潜在第二线标准治疗
礼来(LLY.US)、强生(JNJ.US)与辉瑞(PFE.US)拓展中国市场：旗下创新药物纳入首版商保目录
智通财经 · 12-08
礼来(LLY.US)、强生(JNJ.US)与辉瑞(PFE.US)拓展中国市场：旗下创新药物纳入首版商保目录
2025国谈落地：双管齐下 从“用得上”走向“用得起”
21世纪经济报道 · 12-08
2025国谈落地：双管齐下 从“用得上”走向“用得起”
AI制药，炒作还是革命？权威媒体：调查400位业内人士，发现了行业真相
智药局 · 12-06
AI制药，炒作还是革命？权威媒体：调查400位业内人士，发现了行业真相
2026年1月1日起，强生将迎来重大重组！
药智医械 · 12-06
2026年1月1日起，强生将迎来重大重组！
巴克莱上调强生目标价至197美元
格隆汇 · 12-03
巴克莱上调强生目标价至197美元
阿尔茨海默病研发不易，诺和诺德、强生新药试验接连失败！
制药网 · 12-02
阿尔茨海默病研发不易，诺和诺德、强生新药试验接连失败！
创新高！华尔街看涨情绪浓厚 强生(JNJ.US)市值首破5000亿美元
智通财经 · 11-27
创新高！华尔街看涨情绪浓厚 强生(JNJ.US)市值首破5000亿美元
2025年，药企已达成4起超百亿元收购！
制药网 · 11-25
2025年，药企已达成4起超百亿元收购！
强生(JNJ.US)first-in-class新药在国内申报上市 CDE将其纳入拟优先审评
智通财经 · 11-20
强生(JNJ.US)first-in-class新药在国内申报上市 CDE将其纳入拟优先审评
FDA给予Daratumumab和Hyaluronidase-Fihj传统批准，用于新诊断的轻链淀粉样变病
美股速递 · 11-20
FDA给予Daratumumab和Hyaluronidase-Fihj传统批准，用于新诊断的轻链淀粉样变病
强生表示FDA批准Caplyta作为辅助抑郁症治疗药物
投资观察 · 11-20
强生表示FDA批准Caplyta作为辅助抑郁症治疗药物
暂无数据
公司概况
公司名称：
强生
所属市场：
NYSE
上市日期：
--
主营业务：
强生公司于1887年在新泽西州注册成立。强生公司及其子公司从事医疗保健领域各种产品的研发、制造和销售。强生公司是一家控股公司，旗下运营公司几乎遍布全球所有国家。公司的主要重点是与人类健康和福祉相关的产品。公司分为两个业务部门：创新医学和医疗技术。
发行价格：
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23:50","pubTimestamp":1765381800,"startTime":"0","endTime":"0","summary":"强生（JNJ）周三早盘上涨1.7%，此前有报告称该公司的Tecvayli联合Darzalex相比标准方案将疾病进展或死亡风险降低83%，或支持更早线使用；随着治疗范式演变，Carvykti的合作方传奇生物（LEGN）也受到关注。\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 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III Majestec-3 研究的前所未有结果支持 Tecvayli® 联合 Darzalex Faspro® 作为复发/难治性多发性骨髓瘤患者的潜在第二线标准治疗","url":"https://stock-news.laohu8.com/highlight/detail?id=1192770072","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1192770072?lang=zh_cn&edition=full","pubTime":"2025-12-09 20:47","pubTimestamp":1765284461,"startTime":"0","endTime":"0","summary":"阶段 III Majestec-3 研究的前所未有结果支持 Tecvayli® 联合 Darzalex Faspro® 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