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

交易中 12-16 12:07:15 EST

6.04

+0.06

+0.92%

最高6.08	最低5.98	成交量9.03万
今开5.98	昨收5.98	日振幅1.59%
总市值2.89亿	流通市值2.07亿	总股本4,788万
成交额54.57万	换手率0.26%	流通股本3,423万
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北京优虎网络科技有限公司

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2025年11月12日签订独家许可协议。根据许可协议的条款及条件，齐鲁制药获得在中国地区进行LAE002的研究、开发及商业化的独家许可。","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://www.zhitongcaijing.com/content/detail/1381311.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["HR","III","BK4225","BK4203","BK1161","02105","BK4134"],"gpt_icon":0},{"id":"2591865967","title":"复星医药控股子公司酮洛芬贴剂获准开展III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2591865967","media":"中金财经","labels":["executive"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2591865967?lang=zh_cn&edition=full","pubTime":"2025-12-14 08:13","pubTimestamp":1765671185,"startTime":"0","endTime":"0","summary":"中访网数据 上海复星医药(集团)股份有限公司于2025年12月12日发布公告，其控股子公司上海朝晖药业有限公司研发的酮洛芬贴剂，已获得国家药品监督管理局批准，将在中国境内开展III期临床试验。　　该事件的影响范围主要集中于复星医药集团及其控股子公司朝晖药业的研发管线推进，以及未来潜在的非甾体抗炎药外用贴剂市场。","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/ggzixun/20251214/31864526.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":"zhongjincaijing_highlight","symbols":["BK0196","600196","BK0239","BK0187","BK0012","BK0060","BK0188","BK1191","BK4134","BK0096","BK0183","III","02196","BK1515","BK0175","BK0028","BK1593"],"gpt_icon":0},{"id":"2589352213","title":"中慧生物-B(02627)：冻干人用狂犬病疫苗(人二倍体细胞)的III期临床试验启动","url":"https://stock-news.laohu8.com/highlight/detail?id=2589352213","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2589352213?lang=zh_cn&edition=full","pubTime":"2025-12-08 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G12D抑制剂单药对照化疗III期研究","url":"https://stock-news.laohu8.com/highlight/detail?id=2589885635","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2589885635?lang=zh_cn&edition=full","pubTime":"2025-12-05 08:16","pubTimestamp":1764893771,"startTime":"0","endTime":"0","summary":"智通财经APP讯，劲方医药-B 发布公告，口服KRAS G12D 抑制剂GFH375治疗经治 KRAS G12D突变型转移性胰腺癌患者的注册性III期试验已在北京大学肿瘤医院启动。这项多中心、开放标签、随机对照的III期试验将在约40家中心开展，计划入组约320例既往接受至少一种标准系统性治疗的转移性胰腺癌患者。","market":"sh","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://www.zhitongcaijing.com/content/detail/1377969.html","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":"stock_zhitongcaijing","symbols":["BK1574","02595","BK4134","III","09939","BK1515","159938","BK1161"],"gpt_icon":0},{"id":"2589985521","title":"亚盛医药-B(06855)耐立克®一线治疗Ph+ ALL的全球注册III期临床研究获美国FDA和欧洲EMA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2589985521","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2589985521?lang=zh_cn&edition=full","pubTime":"2025-12-05 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III, Ltd. (Nasdaq: KOYN) 与 First Digital Group Ltd. 宣布就拟议业务合并签署意向书，以此打造全球稳定币与数字支付领军企业","url":"https://stock-news.laohu8.com/highlight/detail?id=2588037958","media":"GlobeNewswire","labels":["corporation"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2588037958?lang=zh_cn&edition=full","pubTime":"2025-12-02 19:30","pubTimestamp":1764675000,"startTime":"0","endTime":"0","summary":"公司成立于 2019 年，在 2022 年由总部位于直布罗陀的 First Digital Group Ltd. 完成重组。合并后，新公司计划加快 First Digital 的国际扩张速度，拓展其产品组合，并进一步完善其监管与合规体系。顾问 Cohen & Company Capital Markets 担任 First Digital 的独家资本市场及并购顾问。Loeb & Loeb LLP 担任 KOYN 的法律顾问。","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://www.globenewswire.com/news-release/2025/12/02/3197723/0/zh-hans/CSLM-Digital-Asset-Acquisition-Corp-III-Ltd-Nasdaq-KOYN-%E4%B8%8E-First-Digital-Group-Ltd-%E5%AE%A3%E5%B8%83%E5%B0%B1%E6%8B%9F%E8%AE%AE%E4%B8%9A%E5%8A%A1%E5%90%88%E5%B9%B6%E7%AD%BE%E7%BD%B2%E6%84%8F%E5%90%91%E4%B9%A6-%E4%BB%A5%E6%AD%A4%E6%89%93%E9%80%A0%E5%85%A8%E7%90%83%E7%A8%B3%E5%AE%9A%E5%B8%81%E4%B8%8E%E6%95%B0%E5%AD%97%E6%94%AF%E4%BB%98%E9%A2%86%E5%86%9B%E4%BC%81%E4%B8%9A.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU1668664300.SGD","DAAQ","LU0106831901.USD","KOYN","BK4134","LU1791807156.HKD","DAAQU","LU2360107671.USD","BK4023","CSLM","LU1861220207.SGD","III","LU1861217088.USD"],"gpt_icon":1},{"id":"2588701422","title":"君圣泰医药-B(02511)公布HTD1801与达格列净的头对头III期临床研究结果展现控糖优势及心血管代谢优效获益","url":"https://stock-news.laohu8.com/highlight/detail?id=2588701422","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2588701422?lang=zh_cn&edition=full","pubTime":"2025-12-02 08:03","pubTimestamp":1764633831,"startTime":"0","endTime":"0","summary":"智通财经APP讯，君圣泰医药-B 发布公告，HTD1801在2型糖尿病患者中开展的与达格列净头对头的临床III期试验取得了积极的结果，试验达到主要终点，并在多项关键心血管代谢指标的改善上优于达格列净。试验数据再次验证，HTD1801靶向2型糖尿病发生及发展的根源性问题，实现更全面的心血管代谢综合获益。HTD1801具有良好的安全性与耐受性，严重不良事件的发生率为3.8%。君圣泰医药计划于今年内启动HTD1801项目的新药上市申请。","market":"sh","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://www.zhitongcaijing.com/content/detail/1376294.html","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":"stock_zhitongcaijing","symbols":["BK1161","III","02511","BK4134"],"gpt_icon":0},{"id":"2586720005","title":"东诚药业(002675.SZ)：氟[18F]思睿肽注射液完成III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2586720005","media":"智通财经网","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2586720005?lang=zh_cn&edition=full","pubTime":"2025-11-28 17:27","pubTimestamp":1764322073,"startTime":"0","endTime":"0","summary":"智通财经APP讯，东诚药业(002675.SZ)公告，公司控股子公司烟台蓝纳成生物技术股份有限公司(简称“蓝纳成”)正在研发的氟[18F]思睿肽注射液是一种靶向PSMA的放射性体内诊断药物，适用于下述前列腺癌患者前列腺特异性膜抗原(PSMA)阳性病灶的正电子发射断层扫描(PET)成像：拟接受初始根治性治疗，怀疑存在转移灶的前列腺癌患者;血清前列腺特异性抗原(PSA)水平升高，怀疑生化复发的前列腺癌患者。更多港股重磅资讯，下载智通财经app更多港股及海外理财资讯，请点击www.zhitongcaijing.com（搜索“智通财经”）；欲加入智通港股投资群，请加智通客服微信(ztcjkf)","market":"sh","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://www.zhitongcaijing.com/content/detail/1375135.html","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":"highlight_zhitongcaijin","symbols":["002675","BK4134","III","BK0239"],"gpt_icon":0},{"id":"2586219474","title":"港股异动 | 宜明昂科-B(01541)午后涨超9% IMM0306的III期临床研究方案获CDE许可","url":"https://stock-news.laohu8.com/highlight/detail?id=2586219474","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2586219474?lang=zh_cn&edition=full","pubTime":"2025-11-27 13:52","pubTimestamp":1764222736,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，宜明昂科-B(01541)午后涨超9%，截至发稿，涨7.98%，报7.31港元，成交额1070.04万港元。消息面上，宜明昂科午间公告，公司已获得国家药监局药品审评中心批准IMM0306联合来那度胺治疗复发/难治性滤泡性淋巴瘤的III期临床研究方案，标志着复发/难治性滤泡性淋巴瘤创新疗法的发展加速。据悉，IMM0306是全球首个进入临床阶段的CD47和CD20双靶向双特异性分子，可阻断“别吃我”信号，激活巨噬细胞和NK细胞，优先结合CD20而非CD47，有效消除恶性B细胞，同时将毒性降至最低，从而可改善治疗效果。公司拥有IMM0306的全球知识产权及商业化权利。","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://www.zhitongcaijing.com/content/detail/1374362.html","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":"stock_zhitongcaijing","symbols":["LU1223082196.USD","BK4134","LU1223083913.SGD","CDE","III","BK1161","LU1223082519.USD","01541","BK4017"],"gpt_icon":0},{"id":"2586970219","title":"港股异动 | 基石药业-B(02616)现涨超5% 欧盟委员会批准舒格利单抗用于治疗III期非小细胞肺癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2586970219","media":"智通财经","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2586970219?lang=zh_cn&edition=full","pubTime":"2025-11-27 13:43","pubTimestamp":1764222201,"startTime":"0","endTime":"0","summary":"消息面上，基石药业宣布，欧盟委员会已批准舒格利单抗的新适应症：单药治疗肿瘤细胞PD-L1表达≥1%、无EGFR敏感突变或ALK、ROS1基因组变异、在含铂放化疗后未出现疾病进展的、不可切除的III期非小细胞肺癌成人患者。基石药业将继续推进舒格利单抗在全球的可及性，践行对患者的长期承诺。","market":"sh","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://www.zhitongcaijing.com/content/detail/1374355.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1161","02616","BK4134","BK1574","III"],"gpt_icon":0},{"id":"2586215237","title":"宜明昂科-B(01541)：药品审评中心批准IMM0306治疗复发╱难治性滤泡性淋巴瘤的III期临床研究方案","url":"https://stock-news.laohu8.com/highlight/detail?id=2586215237","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2586215237?lang=zh_cn&edition=full","pubTime":"2025-11-27 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后续拟申报上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2586284330","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2586284330?lang=zh_cn&edition=full","pubTime":"2025-11-26 11:09","pubTimestamp":1764126584,"startTime":"0","endTime":"0","summary":"消息面上，君实生物宣布，由公司自主研发的特瑞普利单抗注射液对比特瑞普利单抗注射液联合化疗一线治疗复发或转移性非鳞状非小细胞肺癌的多中心、开放、随机对照Ⅲ期临床研究达到主要研究终点。君实生物计划将于近期向监管部门递交该产品的上市许可申请。公开资料显示，JS001sc是公司在已上市产品特瑞普利单抗注射液的基础上开发的皮下注射制剂，为首款进入III期临床研究阶段的国产抗 PD-1 单抗皮下制剂，有望给患者带来用药的便捷性。","market":"sh","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://www.zhitongcaijing.com/content/detail/1373733.html","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":"stock_zhitongcaijing","symbols":["BK1515","688180","BK1161","01877","BK0239","BK4134","III","BK1583"],"gpt_icon":0},{"id":"2586540410","title":"港股异动 | 君实生物(01877)现涨近5% JS001sc肺癌III期临床达主要终点 公司近期将递交上市许可申请","url":"https://stock-news.laohu8.com/highlight/detail?id=2586540410","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2586540410?lang=zh_cn&edition=full","pubTime":"2025-11-25 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| 和誉-B(02256)尾盘涨超4% 公司展示匹米替尼临床III期MANEUVER研究长期疗效和安全性数据","url":"https://stock-news.laohu8.com/highlight/detail?id=2584900001","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2584900001?lang=zh_cn&edition=full","pubTime":"2025-11-20 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