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III 信息服务
交易中 12-30 10:13:06 EST
5.88
-0.18
-3.05%
最高
6.05
最低
5.88
成交量
4.10万
今开
6.05
昨收
6.06
日振幅
2.93%
总市值
2.81亿
流通市值
2.01亿
总股本
4,788万
成交额
24.33万
换手率
0.12%
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
--
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
汇量科技(01860)因PAGAC III Munich Holding (Cayman)Limited行使换股权发行约4746万股换股股份
智通财经 · 19:03
汇量科技(01860)因PAGAC III Munich Holding (Cayman)Limited行使换股权发行约4746万股换股股份
智飞生物德谷门冬双胰岛素注射液完成III期临床试验,有效性及安全性与原研药相当
中金财经 · 12-29 17:34
智飞生物德谷门冬双胰岛素注射液完成III期临床试验,有效性及安全性与原研药相当
北京软件和信息服务业协会AIGC工作委员会启动
北京商报 · 12-25
北京软件和信息服务业协会AIGC工作委员会启动
前11个月,崂山区规上软件信息服务业营收规模突破126亿元
观海新闻 · 12-24
前11个月,崂山区规上软件信息服务业营收规模突破126亿元
华硕GPU Tweak III新版发布:修复NVIDIA驱动问题、新增1%及0.1% Low帧
快科技 · 12-22
华硕GPU Tweak III新版发布:修复NVIDIA驱动问题、新增1%及0.1% Low帧
核药进展如潮涌!远大医药(00512)创新RDC药物TLX591-CDx国内III期达到主要临床终点,诊疗一体化布局蓄势待发
智通财经 · 12-21
核药进展如潮涌!远大医药(00512)创新RDC药物TLX591-CDx国内III期达到主要临床终点,诊疗一体化布局蓄势待发
远大医药(00512)用于诊断前列腺癌的创新在研放射性核素偶联药物TLX591-CDx中国 III 期临床研究成功达到主要临床终点
智通财经 · 12-21
远大医药(00512)用于诊断前列腺癌的创新在研放射性核素偶联药物TLX591-CDx中国 III 期临床研究成功达到主要临床终点
天坛生物旗下成都蓉生重组八因子新药启动III期临床
中金财经 · 12-20
天坛生物旗下成都蓉生重组八因子新药启动III期临床
G-III服装集团盘中异动 下午盘大幅下挫5.00%报30.01美元
市场透视 · 12-20
G-III服装集团盘中异动 下午盘大幅下挫5.00%报30.01美元
阿斯利康甲磺酸奥希替尼片启动II期临床 适应症为不适合或拒绝化疗的EGFR常见突变阳性III期不可切除NSCLC患者
新浪财经 · 12-19
阿斯利康甲磺酸奥希替尼片启动II期临床 适应症为不适合或拒绝化疗的EGFR常见突变阳性III期不可切除NSCLC患者
港股异动 | 诺诚健华(09969)涨超4% 自研新型TYK2抑制剂ICP-332治疗CSU获批准开展II/III期临床试验
智通财经 · 12-19
港股异动 | 诺诚健华(09969)涨超4% 自研新型TYK2抑制剂ICP-332治疗CSU获批准开展II/III期临床试验
新诺威(300765.SZ)子公司司库奇尤单抗注射液III期临床试验获得顶线分析数据
智通财经 · 12-18
新诺威(300765.SZ)子公司司库奇尤单抗注射液III期临床试验获得顶线分析数据
III期ARTISTRY-2研究达主要终点,吉利德新型HIV二联疗法展现潜力
药事纵横 · 12-18
III期ARTISTRY-2研究达主要终点,吉利德新型HIV二联疗法展现潜力
来凯医药-B(02105):LAE002 (AFURESERTIB)针对HR+/HER2-局部晚期或转移性乳腺癌的III期临床试验(AFFIRM-205)已完成入组
智通财经 · 12-15
来凯医药-B(02105):LAE002 (AFURESERTIB)针对HR+/HER2-局部晚期或转移性乳腺癌的III期临床试验(AFFIRM-205)已完成入组
复星医药控股子公司酮洛芬贴剂获准开展III期临床试验
中金财经 · 12-14
复星医药控股子公司酮洛芬贴剂获准开展III期临床试验
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
智通财经 · 12-08
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
劲方医药-B(02595):GFH375治疗转移性胰腺癌注册性临床试验在首家研究中心启动 为全球首个口服KRAS G12D抑制剂单药对照化疗III期研究
智通财经 · 12-05
劲方医药-B(02595):GFH375治疗转移性胰腺癌注册性临床试验在首家研究中心启动 为全球首个口服KRAS G12D抑制剂单药对照化疗III期研究
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
智通财经 · 12-05
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
CSLM Digital Asset Acquisition Corp 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
GlobeNewswire · 12-02
CSLM Digital Asset Acquisition Corp 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
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
智通财经 · 12-02
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
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公司概况
公司名称:
信息服务
所属市场:
NASDAQ
上市日期:
--
主营业务:
Information Services Group, Inc.于2006年7月20日在特拉华州注册成立。该公司是一家全球领先的技术研究和咨询公司。ISG是超过900家客户、超过75家百强企业值得信赖的商业伙伴,致力于帮助企业、公共部门组织以及服务和技术提供商实现卓越运营和更快增长。该公司专门从事数字化转型服务,包括自动化、云和数据分析;采购咨询;托管治理和风险服务;网络载体服务;技术战略和运营设计;变革管理;市场情报和技术研究与分析。
发行价格:
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Low帧统计。","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":"https://tech.ifeng.com/c/8pI15Vzje5c","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"fenghuang_stock","symbols":["BK4134","III"],"gpt_icon":0},{"id":"2593212811","title":"核药进展如潮涌!远大医药(00512)创新RDC药物TLX591-CDx国内III期达到主要临床终点,诊疗一体化布局蓄势待发","url":"https://stock-news.laohu8.com/highlight/detail?id=2593212811","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2593212811?lang=zh_cn&edition=full","pubTime":"2025-12-21 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期临床研究成功达到主要临床终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2593512143","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2593512143?lang=zh_cn&edition=full","pubTime":"2025-12-21 18:10","pubTimestamp":1766311834,"startTime":"0","endTime":"0","summary":"智通财经APP讯,远大医药 公布,集团用于诊断前列腺癌的创新在研放射性核素偶联药物 TLX591-CDx 在中国进行的 III 期临床试验,近日取得了积极的顶线结果,并成功达到了主要临床终点。这表明 TLX591-CDx 的 PET 成像检测对临床决策具有重要影响,可优化疑似生化复发的前列腺癌患者的临床治疗策略。","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":"http://www.zhitongcaijing.com/content/detail/1384112.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":["BK4134","III","00512","BK1191"],"gpt_icon":0},{"id":"2592811181","title":"天坛生物旗下成都蓉生重组八因子新药启动III期临床","url":"https://stock-news.laohu8.com/highlight/detail?id=2592811181","media":"中金财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2592811181?lang=zh_cn&edition=full","pubTime":"2025-12-20 10:42","pubTimestamp":1766198535,"startTime":"0","endTime":"0","summary":"中访网数据 北京天坛生物制品股份有限公司今日公告,其下属企业成都蓉生药业有限责任公司研发的“注射用重组人凝血因子Ⅷ-Fc融合蛋白”已于近日正式启动III期临床试验。该药品注册分类为治疗用生物制品,拟用于A型血友病患者的出血控制、预防及手术出血预防。根据公告,该产品研发累计投入已达9868.32万元。目前,国内市场尚无同类产品上市,国际市场主要有赛诺菲公司的Eloctate和Altuviiio两款产品。该药品后续仍需完成III期临床试验、提交上市申请并通过国家药监部门审评审批,方可实现上市销售。天坛生物提示,药品研发周期长且存在不确定性,投资者需注意相关风险。","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":"http://sc.stock.cnfol.com/ggzixun/20251220/31879523.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":"zhongjincaijing_highlight","symbols":["BK0239","BK4134","BK0168","BK0188","III","BK0082","BK0028","600161","BK0010","BK0046","BK0185"],"gpt_icon":0},{"id":"2592146209","title":"G-III服装集团盘中异动 下午盘大幅下挫5.00%报30.01美元","url":"https://stock-news.laohu8.com/highlight/detail?id=2592146209","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2592146209?lang=zh_cn&edition=full","pubTime":"2025-12-20 04:27","pubTimestamp":1766176076,"startTime":"0","endTime":"0","summary":"北京时间2025年12月20日04时27分,G-III服装集团股票出现异动,股价快速跳水5.00%。截至发稿,该股报30.01美元/股,成交量27.949万股,换手率0.66%,振幅4.75%。G-III服装集团股票所在的服装制造行业中,整体跌幅为1.21%。其相关个股中,文斯控股、兰亭集势、Xcel Brands, Inc涨幅较大,儿童之家、金铉集团、雷克兰医疗工业较为活跃,换手率分别为4.78%、3.71%、3.11%,振幅较大的相关个股有文斯控股、兰亭集势、金铉集团,振幅分别为14.49%、14.13%、13.31%。","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=nesSN2025122004275697a080a9&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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18:03","pubTimestamp":1766138580,"startTime":"0","endTime":"0","summary":"本次试验目的是评估不适合或拒绝化疗的EGFRm阳性III期不可切除NSCLC患者在放疗前使用奥希替尼作为诱导治疗及在放疗后继续使用奥希替尼直至疾病进展的有效性。甲磺酸奥希替尼片为化学药物,适应症为不适合或拒绝化疗的EGFR常见突变阳性III期不可切除NSCLC患者。","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=nesSN20251219185751a6b6da17&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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自研新型TYK2抑制剂ICP-332治疗CSU获批准开展II/III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2592134408","media":"智通财经","labels":["productRelease","dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2592134408?lang=zh_cn&edition=full","pubTime":"2025-12-19 11:17","pubTimestamp":1766114258,"startTime":"0","endTime":"0","summary":"消息面上,12月18日,据诺诚健华官微消息,公司宣布,自主研发的新型TYK2抑制剂soficitinib治疗慢性自发性荨麻疹获国家药品监督管理局药品审评中心批准开展II/III期临床试验。Soficitinib是诺诚健华自主研发的高效、高选择性的新型口服TYK2抑制剂,开发用于治疗多种T细胞相关的自身免疫性疾病,目前开发的适应症深度布局皮肤科这一广阔的市场,包括特应性皮炎、白癜风、结节性痒疹、荨麻疹等。","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/1383531.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease,dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["III","BK4134","688428","BK1161","BK1574","BK0239","09969"],"gpt_icon":0},{"id":"2592973845","title":"新诺威(300765.SZ)子公司司库奇尤单抗注射液III期临床试验获得顶线分析数据","url":"https://stock-news.laohu8.com/highlight/detail?id=2592973845","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2592973845?lang=zh_cn&edition=full","pubTime":"2025-12-18 15:45","pubTimestamp":1766043917,"startTime":"0","endTime":"0","summary":"智通财经APP讯,新诺威 发布公告,公司的控股子公司石药集团巨石生物制药有限公司开发的司库奇尤单抗注射液于近日在III期临床试验中获得顶线分析数据。该产品是巨石生物开发的全人源IgG1单克隆抗体药物,为可善挺的生物类似药。可善挺在中国获批的适应症包括6岁及以上斑块状银屑病、银屑病关节炎、强直性脊柱炎及化脓性汗腺炎,其疗效与安全性已获得广泛认可。有关详细数据将于后续学术会议及期刊上发布。","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://www.zhitongcaijing.com/content/detail/1383061.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":["III","300765","BK0226","BK4134"],"gpt_icon":0},{"id":"2592902308","title":"III期ARTISTRY-2研究达主要终点,吉利德新型HIV二联疗法展现潜力","url":"https://stock-news.laohu8.com/highlight/detail?id=2592902308","media":"药事纵横","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2592902308?lang=zh_cn&edition=full","pubTime":"2025-12-18 07:05","pubTimestamp":1766012717,"startTime":"0","endTime":"0","summary":"12月15日,吉利德宣布III期ARTISTRY-2研究取得积极顶线结果。吉利德计划将ARTISTRY研究的III期结果提交给监管机构,并将在未来的科学大会上公布详细数据。在ARTISTRY-2研究中,每日一次的单片复方方案BIC/LEN达到了主要成功标准,其疗效非劣于BIKTARVY。ARTISTRY-2的研究结果将与III期ARTISTRY-1研究的发现共同构成监管申报的基础。吉利德已于2025年11月公布了ARTISTRY-1的顶线结果,显示BIC/LEN组合耐受性良好,在疗效上非劣于多片式抗反转录病毒治疗方案。目前尚无治愈HIV或艾滋病的方法。","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=nesSN20251218071039a6afa5d0&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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(AFURESERTIB)针对HR+/HER2-局部晚期或转移性乳腺癌的III期临床试验(AFFIRM-205)已完成入组","url":"https://stock-news.laohu8.com/highlight/detail?id=2591869882","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2591869882?lang=zh_cn&edition=full","pubTime":"2025-12-15 08:17","pubTimestamp":1765757864,"startTime":"0","endTime":"0","summary":"智通财经APP讯,来凯医药-B 发布公告,集团已完成LAE002联合氟维司群针对治疗HR+/HER2-局部晚期或转移性乳腺癌伴随 PIK3CA/AKT1/PTEN基因改变患者的III期临床试验AFFIRM-205入组。III 期临床试验AFFIRM-205为一项多中心、随机、双盲、安慰剂对照的关键性研究,旨在评估该联合疗法的抗肿瘤疗效及安全性。集团与齐鲁制药有限公司已于 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":["02196","BK0188","BK0060","BK1191","BK0239","BK1515","BK0175","BK1593","BK4134","III","BK0183","600196","BK0196","BK0012","BK0187","BK0028","BK0096"],"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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