新桥生物(NBP)_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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NBP 新桥生物

已收盘 07-06 16:00:00 EDT

2.01

-0.13

-6.07%

盘后2.00

-0.01-0.50%

19:59 EDT

最高2.26	最低1.99	成交量87.33万
今开2.26	昨收2.14	日振幅12.85%
总市值2.32亿	流通市值1.30亿	总股本1.15亿
成交额181.07万	换手率1.35%	流通股本6,448万
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--

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北京优虎网络科技有限公司

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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.laohu8.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.laohu8.com/m/news/1120501405?lang=zh_cn&edition=full","pubTime":"2026-03-16 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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":["NBP","BK4139"],"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.laohu8.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.laohu8.com/m/news/1106527073?lang=zh_cn&edition=full","pubTime":"2026-03-16 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Biosciences）近日披露，该公司与美国食品药品监督管理局（FDA）针对其在研药物Givastomig用于治疗胃腺癌的加速批准路径，成功举行了一场富有成效的B类会议。\n此次会议重点探讨了Givastomig通过加速审批通道上市的可能性，双方就后续临床开发策略及数据要求达成重要共识。该进展标志着Givastomig在胃腺癌治疗领域的商业化进程迈出关键一步。","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":"1184660068","title":"新桥生物公布二期a阶段顶线数据：Vis-101为湿性年龄相关性黄斑变性提供快速、强劲且持久的治疗反应","url":"https://stock-news.laohu8.com/highlight/detail?id=1184660068","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1184660068?lang=zh_cn&edition=full","pubTime":"2026-03-09 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19:02","pubTimestamp":1773054140,"startTime":"0","endTime":"0","summary":"新桥生物近日公布了其候选药物Vis-101的临床试验数据，结果显示其在治疗相关眼部疾病方面取得了显著成效。\n数据显示，接受Vis-101治疗的患者群体，其最佳矫正视力出现了具有临床意义的提升，平均改善幅度超过了10个ETDRS字母。与此同时，患者的中位中心凹厚度也呈现出显著下降，降低范围在100至150微米之间。\n这些积极的数据指标，为Vis-101后续的临床开发路径提供了有力的支持。","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":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","NBP"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1132480297","title":"新桥生物任命生物技术领袖埃米特·T·坎宁安博士为董事会副主席，加速全球生物技术平台发展","url":"https://stock-news.laohu8.com/highlight/detail?id=1132480297","media":"美股速递","labels":["executive"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1132480297?lang=zh_cn&edition=full","pubTime":"2026-02-19 20:02","pubTimestamp":1771502522,"startTime":"0","endTime":"0","summary":"新桥生物宣布任命生物技术领域的杰出领导者埃米特·T·坎宁安博士为董事会副主席。这一重要人事任命旨在进一步加速公司全球生物技术平台的拓展与创新。坎宁安博士在医学、科研及公共卫生领域拥有深厚的学术背景和丰富的行业经验，他的加入将为新桥生物的战略发展注入强劲动力。","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":"executive","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","NBP"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1106070252","title":"新桥生物全球首例患者入组：Givastomig联合免疫化疗治疗一线转移性胃癌的随机二期研究启动","url":"https://stock-news.laohu8.com/highlight/detail?id=1106070252","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1106070252?lang=zh_cn&edition=full","pubTime":"2026-02-18 05:07","pubTimestamp":1771362463,"startTime":"0","endTime":"0","summary":"新桥生物宣布，其全球性、随机二期临床研究已完成首例患者给药。该研究旨在评估Givastomig与免疫化疗联合方案，用于一线治疗转移性胃癌患者的疗效与安全性。","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":"2610254671","title":"新桥生物盘中异动 早盘急速下挫5.19%","url":"https://stock-news.laohu8.com/highlight/detail?id=2610254671","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2610254671?lang=zh_cn&edition=full","pubTime":"2026-02-10 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