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INCY 因塞特医疗
休市中 02-13 16:00:00 EST
101.10
+0.35
+0.35%
盘后
98.64
-2.46
-2.43%
19:56 EST
最高
103.18
最低
100.53
成交量
138.47万
今开
101.47
昨收
100.75
日振幅
2.63%
总市值
201.20亿
流通市值
164.84亿
总股本
1.99亿
成交额
1.41亿
换手率
0.85%
流通股本
1.63亿
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
因塞特医疗高管透露：FDA一月告知公司，Opzelura需进行额外疗效研究方可获批结节性痒疹适应症
美股速递 · 02-10
因塞特医疗高管透露：FDA一月告知公司，Opzelura需进行额外疗效研究方可获批结节性痒疹适应症
因塞特高管表示：到2030年，剔除Jakafi后的核心业务规模有望达到当前Jakafi水平
美股速递 · 02-10
因塞特高管表示：到2030年，剔除Jakafi后的核心业务规模有望达到当前Jakafi水平
异动解读 | 因塞特医疗盘前大跌近12%，2026年收入预期疲软加剧专利到期担忧
异动解读 · 02-10
异动解读 | 因塞特医疗盘前大跌近12%，2026年收入预期疲软加剧专利到期担忧
华尔街顶级分析师最新评级：微软遭下调，Snap获上调
环球市场播报 · 02-06
华尔街顶级分析师最新评级：微软遭下调，Snap获上调
因塞特医疗宣布Zynyz®获欧盟CHMP积极意见，用于晚期肛管鳞状细胞癌一线治疗
美股速递 · 01-30
因塞特医疗宣布Zynyz®获欧盟CHMP积极意见，用于晚期肛管鳞状细胞癌一线治疗
因塞特医疗股价盘前涨2.8%，血癌疗法达晚期试验主要终点
美股速递 · 01-05
因塞特医疗股价盘前涨2.8%，血癌疗法达晚期试验主要终点
因塞特医疗计划于2026年上半年提交Tafasitamab一线治疗新诊断DLBCL成人患者的补充生物制剂许可申请
美股速递 · 01-05
因塞特医疗计划于2026年上半年提交Tafasitamab一线治疗新诊断DLBCL成人患者的补充生物制剂许可申请
因塞特医疗公布Tafasitamab（Monjuvi®/Minjuvi®）作为弥漫性大B细胞淋巴瘤一线治疗关键研究的积极顶线结果
美股速递 · 01-05
因塞特医疗公布Tafasitamab（Monjuvi®/Minjuvi®）作为弥漫性大B细胞淋巴瘤一线治疗关键研究的积极顶线结果
因塞特医疗在日本获批Zynyz®（Retifanlimab）用于晚期肛门癌的一线治疗
美股速递 · 2025-12-22
因塞特医疗在日本获批Zynyz®（Retifanlimab）用于晚期肛门癌的一线治疗
因塞特医疗宣布Minjuvi®（Tafasitamab）与利妥昔单抗及来那度胺联合用于治疗复发或难治性滤泡淋巴瘤获得批准
美股速递 · 2025-12-22
因塞特医疗宣布Minjuvi®（Tafasitamab）与利妥昔单抗及来那度胺联合用于治疗复发或难治性滤泡淋巴瘤获得批准
AI狂欢过后如何备战2026？这四只“攻守兼备”的防御性股票值得关注
智通财经 · 2025-12-19
AI狂欢过后如何备战2026？这四只“攻守兼备”的防御性股票值得关注
因塞特医疗宣布Minjuvi®（Tafasitamab）获欧洲委员会批准用于治疗复发性或难治性滤泡性淋巴瘤
美股速递 · 2025-12-18
因塞特医疗宣布Minjuvi®（Tafasitamab）获欧洲委员会批准用于治疗复发性或难治性滤泡性淋巴瘤
因塞特医疗：HervÉ Hoppenot于12月10日通知即刻退休，辞去公司董事会职务
美股速递 · 2025-12-13
因塞特医疗：HervÉ Hoppenot于12月10日通知即刻退休，辞去公司董事会职务
因塞特医疗在2025年ASH大会上发布更新的积极数据，巩固了其首个靶向Mutcalr单克隆抗体Inca033989在原发性血小板增多症患者中的潜力
美股速递 · 2025-12-09
因塞特医疗在2025年ASH大会上发布更新的积极数据，巩固了其首个靶向Mutcalr单克隆抗体Inca033989在原发性血小板增多症患者中的潜力
因塞特医疗公布首款Mutcalr靶向单克隆抗体Inca033989在骨髓纤维化患者中的积极新数据，发布于2025年ASH会议
美股速递 · 2025-12-07
因塞特医疗公布首款Mutcalr靶向单克隆抗体Inca033989在骨髓纤维化患者中的积极新数据，发布于2025年ASH会议
因塞特医疗公布Minjuvi®（Tafasitamab）治疗复发性或难治性滤泡淋巴瘤的积极CHMP意见
美股速递 · 2025-11-17
因塞特医疗公布Minjuvi®（Tafasitamab）治疗复发性或难治性滤泡淋巴瘤的积极CHMP意见
摩根士丹利：这些“潜在分红股”若启动派息，或将带来可观回报
老虎资讯综合 · 2025-11-11
摩根士丹利：这些“潜在分红股”若启动派息，或将带来可观回报
Prelude Therapeutics与因塞特医疗签署独家选择权协议以推进选择性Jak2v617f Jh2抑制剂
美股速递 · 2025-11-04
Prelude Therapeutics与因塞特医疗签署独家选择权协议以推进选择性Jak2v617f Jh2抑制剂
因塞特医疗公布Opzelura®（Ruxolitinib Cream）在中度特应性皮炎成人患者中进行的3B期True-AD4试验新数据
美股速递 · 2025-10-26
因塞特医疗公布Opzelura®（Ruxolitinib Cream）在中度特应性皮炎成人患者中进行的3B期True-AD4试验新数据
因塞特医疗：加拿大卫生部批准Opzelura（鲁索替尼）乳膏用于2-11岁儿童特应性皮炎治疗
美股速递 · 2025-10-15
因塞特医疗：加拿大卫生部批准Opzelura（鲁索替尼）乳膏用于2-11岁儿童特应性皮炎治疗
暂无数据
公司概况
公司名称：
因塞特医疗
所属市场：
NASDAQ
上市日期：
--
主营业务：
因塞特医疗公司于1991年在特拉华州注册成立。该公司是一家全球生物制药公司，从事专有疗法的发现、开发和商业化。其研究和商业努力集中在三个治疗领域：血液学、肿瘤学、炎症和自身免疫。
发行价格：
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21:32","pubTimestamp":1770730333,"startTime":"0","endTime":"0","summary":"因塞特医疗高管近日披露，美国食品药品监督管理局已于今年1月正式通知公司，其研发的Opzelura药物在获批用于治疗结节性痒疹之前，必须完成另一项疗效验证研究。这一要求意味着该药物针对此适应症的上市进程将面临新的监管审查环节。","market":"us","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":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4532","BK4588","BK4139","INCY","BK4585","BK4550"],"gpt_icon":0},{"id":"1100720582","title":"因塞特高管表示：到2030年，剔除Jakafi后的核心业务规模有望达到当前Jakafi水平","url":"https://stock-news.laohu8.com/highlight/detail?id=1100720582","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1100720582?lang=zh_cn&edition=full","pubTime":"2026-02-10 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00:40","pubTimestamp":1770309654,"startTime":"0","endTime":"0","summary":"华尔街最受关注、能推动市场走势的研究报告现已汇总于此。以下由 The Fly 整理的今日投资者需重点关注的分析师评级调整。B． Riley：将 Snap评级从中性上调至买入，目标价维持10 美元不变。四季度财报发布后，该机构发现 Snap 多项核心举措已现积极进展，包括高端订阅收入持续强劲增长，以及高利润率广告形式的落地推广。美银：首次覆盖波泰科科学，给予买入评级，目标价38 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