信息服务(III)_个股概要_股票价格_最新资讯_行情走势_历史数据 - 老虎社区

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III 信息服务

盘后交易 02-04 19:36:19 EST

5.29

-0.12

-2.22%

盘后5.29

+0.000.00%

18:02 EST

最高5.54	最低5.28	成交量42.62万
今开5.46	昨收5.41	日振幅4.71%
总市值2.53亿	流通市值1.81亿	总股本4,788万
成交额227.84万	换手率1.25%	流通股本3,423万
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--

数据加载中...

北京优虎网络科技有限公司

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核心产品普美昔替尼凝胶已完成III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2605316104","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2605316104?lang=zh_cn&edition=full","pubTime":"2026-01-22 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CAR-T疗法启动III期临床，治疗自免疾病","url":"https://stock-news.laohu8.com/highlight/detail?id=2605435278","media":"细胞治疗前沿","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2605435278?lang=zh_cn&edition=full","pubTime":"2026-01-21 09:53","pubTimestamp":1768960424,"startTime":"0","endTime":"0","summary":"近日，美国临床试验收录网显示，百时美施贵宝的 CD19 CAR-T 细胞疗法 Zola-cel启动了首个 Ⅲ 期临床试验，治疗活动性系统性硬化症。Zola-cel是BMS基于NEX-T平台开发的一款CD19 CAR-T细胞疗法，于2020年进入临床阶段。2019年，BMS以740亿美元完成对Celgene的收购，借此将两款关键CAR-T疗法Breyanzi与Abecma纳入其产品管线，正式踏入细胞治疗领域。BMS积极布局，不断强化其在下一代细胞治疗领域的战略纵深。","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=nesSN2026012110365897a2adbb&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, 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III期研究的结果于《柳叶刀》发表。SACHI是一项赛沃替尼和奥希替尼的联合疗法，用于治疗伴有MET扩增的接受一线表皮生长因子受体酪氨酸激酶抑制剂治疗后疾病进展的EGFR突变阳性局部晚期或转移性非小细胞肺癌患者的III期研究。基于SACHI研究的数据，赛沃替尼和奥希替尼的联合疗法已于2025年6月在中国获批。","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=nesSN20260116232631a72389bb&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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III期研究结果于《柳叶刀》发表","url":"https://stock-news.laohu8.com/highlight/detail?id=2603554869","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603554869?lang=zh_cn&edition=full","pubTime":"2026-01-16 11:03","pubTimestamp":1768532615,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，和黄医药再涨超4%，月内累计涨幅超20%。消息面上，和黄医药宣布，SACHI 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TKI，由阿斯利康与和黄医药共同开发，并由阿斯利康商业化。基于SACHI研究的数据，赛沃替尼和奥希替尼的联合疗法已于2025年6月在中国获批。","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":"https://finance.sina.com.cn/stock/hkstock/marketalerts/2026-01-15/doc-inhhiyxt4368442.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"sina","symbols":["BK4588","BK4531","HCM","BK1191","BK1588","III","BK4134","00013","BK4585","BK4007","BK1587"],"gpt_icon":0},{"id":"2603628850","title":"艾美疫苗(06660)：迭代工艺高效价人二倍体狂犬疫苗完成III期临床现场工作","url":"https://stock-news.laohu8.com/highlight/detail?id=2603628850","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603628850?lang=zh_cn&edition=full","pubTime":"2026-01-15 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期临床试验SCOUT-HCM取得阳性结果","url":"https://stock-news.laohu8.com/highlight/detail?id=2603253613","media":"美通社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603253613?lang=zh_cn&edition=full","pubTime":"2026-01-14 19:55","pubTimestamp":1768391700,"startTime":"0","endTime":"0","summary":"SCOUT-HCM 的阳性研究结果展现了玛伐凯泰有望成为首个用于青少年 oHCM 患者的心肌肌球蛋白抑制剂。青少年oHCM严重损害健康，主要临床表现与运动耐量下降相关。在欧盟，玛伐凯泰获批用于治疗有症状的NYHA心功能分级II-III级的梗阻性肥厚型心肌病成人患者。","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/4863243_ZH63243_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":["LU2242646821.SGD","LU0114720955.EUR","LU1989771016.USD","LU0061475181.USD","HCM","BK4134","BK4585","LU0225284248.USD","LU0225771236.USD","LU1074936037.SGD","LU1261432733.SGD","LU0868494617.USD","LU1291159041.SGD","LU1093756168.USD","LU1093756325.SGD","IE00BJT1NW94.SGD","IE00BJJMRZ35.SGD","LU0306806265.USD","LU1430594728.SGD","LU2125154935.USD","LU0306807586.USD","BK4559","IE00BSNM7G36.USD","LU2242652126.USD","IE00B2B36J28.USD","BK4534","III","LU1571399168.USD","LU0321505868.SGD","LU1670711123.USD","IE0002141913.USD","LU1670710661.SGD","LU1670710588.SGD","LU1718418525.SGD","BMY","LU1868836591.USD","LU1868837136.USD","BK4588","IE0009355771.USD","LU0985481810.HKD","LU0456855351.SGD","LU0321505439.SGD","LU1323610961.USD","LU1585245621.USD","LU1868837300.USD","IE00BFXG1179.USD","LU0096364046.USD","LU1868836914.USD","LU0267386448.USD","LU0237698245.USD"],"gpt_icon":0},{"id":"2603439618","title":"阿斯利康AZD0486启动III期临床 适应症为新诊断的老年或不适合化疗的大B细胞淋巴瘤","url":"https://stock-news.laohu8.com/highlight/detail?id=2603439618","media":"新浪财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603439618?lang=zh_cn&edition=full","pubTime":"2026-01-14 18:03","pubTimestamp":1768384980,"startTime":"0","endTime":"0","summary":"药物临床试验登记与信息公示平台数据显示，AstraZeneca AB/阿斯利康全球研发（中国）有限公司/AstraZeneca Nijmegen B.V.的AZD0486在新诊断为大B细胞淋巴瘤的老年或不适合化疗的受试者中的多中心、开放性、随机III期临床试验已启动。本次试验药AZD0486的剂型、用法用量信息未公示。AZD0486为生物制品，适应症为新诊断的老年或不适合化疗的大B细胞淋巴瘤。大B细胞淋巴瘤是常见的非霍奇金淋巴瘤亚型，进展快，老年或不耐受化疗患者预后较差，需更安全有效的治疗方案。","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=nesSN20260114190129a4c2fc89&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, 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Lancet)》发表","url":"https://stock-news.laohu8.com/highlight/detail?id=2603666888","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603666888?lang=zh_cn&edition=full","pubTime":"2026-01-14 12:11","pubTimestamp":1768363890,"startTime":"0","endTime":"0","summary":"智通财经APP讯，和黄医药 发布公告，公司今日宣布SACHI III期研究的结果于《柳叶刀 》发表。SACHI是一项赛沃替尼和奥希替尼的联合疗法用于治疗伴有MET扩增的接受一线表皮生长因子受体酪氨酸激酶抑制剂治疗后疾病进展的EGFR突变阳性局部晚期或转移性非小细胞肺癌患者的III期研究。基于SACHI研究的数据，赛沃替尼和奥希替尼的联合疗法已于2025年6月在中国获批。中国医学科学院肿瘤医院的王洁教授亦为SACHI 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