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NBP 新桥生物
盘前交易 09-14 04:23:43 EDT
1.59
-0.10
-5.92%
最高
1.71
最低
1.58
成交量
25.28万
今开
1.70
昨收
1.69
日振幅
7.69%
总市值
1.84亿
流通市值
1.03亿
总股本
1.16亿
成交额
40.72万
换手率
0.39%
流通股本
6,456万
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
新桥生物发布2026年上半年财务业绩,彰显管线动能与战略执行力
美股速递 · 08-20
新桥生物发布2026年上半年财务业绩,彰显管线动能与战略执行力
新桥生物将于2026年8月20日(周四)披露2026年上半年财务业绩并发布公司最新动态
美股速递 · 08-14
新桥生物将于2026年8月20日(周四)披露2026年上半年财务业绩并发布公司最新动态
新桥生物旗下Givastomig的注册性三期临床试验最早有望于2026年第四季度启动
美股速递 · 06-16
新桥生物旗下Givastomig的注册性三期临床试验最早有望于2026年第四季度启动
新桥生物Givastomig获FDA快速通道资格,用于一线治疗HER2阴性转移性胃癌
美股速递 · 06-16
新桥生物Givastomig获FDA快速通道资格,用于一线治疗HER2阴性转移性胃癌
新桥生物:FDA确认Givastomig有望符合加速审批资格
美股速递 · 03-16
新桥生物:FDA确认Givastomig有望符合加速审批资格
新桥生物计划于2026年第四季度启动以客观缓解率为主要终点的注册性三期联合试验
美股速递 · 03-16
新桥生物计划于2026年第四季度启动以客观缓解率为主要终点的注册性三期联合试验
新桥生物宣布与FDA就胃腺癌药物Givastomig加速审批路径达成建设性B类会议
美股速递 · 03-16
新桥生物宣布与FDA就胃腺癌药物Givastomig加速审批路径达成建设性B类会议
加载更多
公司概况
公司名称:
新桥生物
所属市场:
NASDAQ
上市日期:
--
主营业务:
新桥生物于2016年6月30日在开曼群岛注册成立。该公司是一家全球生物技术平台,专注于开发创新的免疫肿瘤疗法。其研发管线包括三个临床阶段项目,其中givastomig是一种用于治疗胃癌的CLDN18.2双特异性抗体,是公司的核心产品。通过其子公司Visara,公司还在开发用于视网膜疾病的VIS-101。
发行价格:
--
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Biosciences)计划于2026年8月20日(星期四)公布其2026年上半年财务报告,届时也将同步更新公司业务进展与战略部署。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["NBP","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1199400680","title":"新桥生物旗下Givastomig的注册性三期临床试验最早有望于2026年第四季度启动","url":"https://stock-news.laohu8.com/highlight/detail?id=1199400680","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1199400680?lang=zh_cn&edition=full","pubTime":"2026-06-16 19:01","pubTimestamp":1781607678,"startTime":"0","endTime":"0","summary":"新桥生物(NovaBridge Biosciences)宣布,其核心候选药物Givastomig的注册性三期临床试验,预计最早将于2026年第四季度开始。这一关键性试验的启动,标志着该药物在特定适应症研发进程中迈入决定性阶段,为后续的监管申报和潜在商业化铺平道路。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","NBP"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1148595922","title":"新桥生物Givastomig获FDA快速通道资格,用于一线治疗HER2阴性转移性胃癌","url":"https://stock-news.laohu8.com/highlight/detail?id=1148595922","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1148595922?lang=zh_cn&edition=full","pubTime":"2026-06-16 19:00","pubTimestamp":1781607647,"startTime":"0","endTime":"0","summary":"新桥生物宣布,其研发的Givastomig已获得美国食品药品监督管理局(FDA)授予的快速通道资格,该资格针对的适应症为一线治疗HER2阴性转移性胃癌。此项认定有望加速该药物的研发与审评进程。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","NBP"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1120501405","title":"新桥生物:FDA确认Givastomig有望符合加速审批资格","url":"https://stock-news.laohu8.com/highlight/detail?id=1120501405","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1120501405?lang=zh_cn&edition=full","pubTime":"2026-03-16 20:39","pubTimestamp":1773664740,"startTime":"0","endTime":"0","summary":"美国食品药品监督管理局(FDA)已正式确认,新桥生物(NovaBridge Biosciences)旗下在研药物Givastomig具备潜在资格,有望通过加速审批通道推进上市进程。\n这一进展意味着,若后续临床试验数据积极,Givastomig或可基于替代终点提前获批,从而缩短其进入市场的时间。加速审批路径通常适用于针对严重疾病、且现有治疗选择有限的创新疗法。\n新桥生物表示,将继续与FDA保持密切沟通,积极推进Givastomig的临床开发计划,以期早日为患者提供新的治疗选择。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"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":["BK4139","NBP"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1139570168","title":"新桥生物计划于2026年第四季度启动以客观缓解率为主要终点的注册性三期联合试验","url":"https://stock-news.laohu8.com/highlight/detail?id=1139570168","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1139570168?lang=zh_cn&edition=full","pubTime":"2026-03-16 19:03","pubTimestamp":1773658990,"startTime":"0","endTime":"0","summary":"新桥生物(NovaBridge Biosciences)宣布,公司将于2026年第四季度正式启动一项注册性三期联合疗法临床试验。该试验将采用客观缓解率(ORR)作为主要疗效终点,旨在评估创新疗法组合在目标患者群体中的治疗效果。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["NBP","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1106527073","title":"新桥生物宣布与FDA就胃腺癌药物Givastomig加速审批路径达成建设性B类会议","url":"https://stock-news.laohu8.com/highlight/detail?id=1106527073","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1106527073?lang=zh_cn&edition=full","pubTime":"2026-03-16 19:02","pubTimestamp":1773658924,"startTime":"0","endTime":"0","summary":"新桥生物(NovaBridge 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