美股详情

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7.82

-0.2200-2.74%

盘后：7.850.0300+0.38%19:57 EST

成交量：282.74万

成交额：2,225.27万

市值：7.18亿

市盈率：4.80

高：7.99

开：7.92

低：7.78

收：8.04

52周最高：19.75

52周最低：7.72

股本：9,177.68万

流通股本：8,727.34万

量比：0.59

换手率：3.24%

股息：- -

股息率：- -

每股收益(TTM):1.63

每股收益(LYR):-0.5920

净资产收益率：66.13%

总资产收益率：-0.59%

市净率：2.24

市盈率(LYR):-13.21

数据加载中...

总览公司新闻资讯公告

复宏汉霖PD-1新药“出海”日本最早将于2028年产生销售提成

复宏汉霖携手卫材就抗PD-1单抗汉斯状达成日本市场合作

南方财经网

释放pipeline in a drug潜力 NLRP3能否催生下一个“药王”?

智通财经网

阿斯利康(AZN.US)宣布PD-L1单抗在华获批新适应症针对子宫内膜癌

港股异动 | 维立志博-B(09887)涨超4% PD-L1/4-1BB双抗获FDA快速通道资格

维立志博-B(09887)：维利信™(PD-L1/4-1BB双特异性抗体奥帕替苏米单抗，LBL-024)获美国FDA授予快速通道资格认定

港股异动 | 复宏汉霖(02696)再涨超8% 广谱抗肿瘤PD-L1 ADC HLX43末线食管鳞癌II期数据首次发布

PD-1/VEGF双抗交易热潮回归？荣昌生物签下56亿美元授权

港股异动 | 复宏汉霖(02696)盘中涨超5% 公司首次公布PD-L1 ADC食管鳞状细胞癌Ⅱ期临床数据

维亚臻生物VSA012注射液启动II期临床适应症为活动性狼疮肾炎等疾病

天士力：PD-L1/VEGF双抗的实体瘤适应症IIa期、直肠癌适应症IIb期临床试验正在入组中

科伦博泰生物-B(06990)核心产品TROP2 ADC芦康沙妥珠单抗(SAC-TMT)联合免疫疗法帕博利珠单抗一线治疗PD-L1阳性局部晚期或转移性非小细胞肺癌获NMPA突破性疗法认定

达伯舒新适应症医保落地系晚期pMMR子宫内膜癌唯一医保抗PD-(L)1药物

中国网财经

【新股IPO】国元国际：瀚思艾泰-B(03378)CD47/PD-1双特异性抗体具备独特性建议谨慎申购

康辰药业(603590.SH)：KC1036联合PD-1抗体和含铂化疗一线治疗晚期复发或转移性食管鳞癌Ⅱ期临床研究完成首例受试者入组

产业新闻 | FDA授予百时美施贵宝PD-1疗法组合优先审评资格；创新帕金森病免疫疗法积极试验结果公布

港股异动 | 荣昌生物(09995)盘中涨超7% 公布PD-1/VEGF双抗非小细胞肺癌临床数据

和誉-B(02256)：和誉医药于ESMO Asia 2025公布口服PD-L1抑制剂ABSK043联合 EGFR抑制剂伏美替尼治疗NSCLC的II期临床初步结果

ADC药物与PD-1/VEGF双抗联用再添案例科伦博泰与Crescent达成双向授权协议

每日经济新闻

ADC与PD-1红海之外，宝济药业如何找到生物医药的“第二增长曲线”？

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16:35","pubTimestamp":1770280559,"startTime":"0","endTime":"0","summary":"近期，英硅智能(03696)宣布提名靶向NLRP3的外周限制性抑制剂ISM5059，该候选药物具有新颖母核，由英硅智能自有Pharma.AI平台驱动设计。","market":"sg","thumbnail":"https://img.zhitongcaijing.com/image/20260205/20260205163220_51027.png?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250","type":0,"news_type":0,"thumbnails":["https://img.zhitongcaijing.com/image/20260205/20260205163220_51027.png?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1402047.html","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":"highlight_zhitongcaijin","symbols":["BK4132","BK4135","LU1169590202.USD","PD","AD","BBB","IBD","CNS","LU1169589451.USD","BK4023"],"gpt_icon":0},{"id":"2605290194","title":"阿斯利康(AZN.US)宣布PD-L1单抗在华获批新适应症 针对子宫内膜癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2605290194","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2605290194?lang=zh_cn&edition=fundamental","pubTime":"2026-01-23 14:42","pubTimestamp":1769150545,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，1月22日，阿斯利康宣布，英飞凡已获中国国家药品监督管理局批准，与卡铂和紫杉醇联合用于错配修复缺陷的原发晚期或复发性子宫内膜癌成人患者的一线治疗，随后以本品单药维持治疗。截至目前该药已在美国获批 10 项适应症，在欧盟获批 11 项适应症，在国内获批 7 项。安全性方面，度伐利尤单抗联合化疗方案的总体安全性和耐受性良好，并且与此前临床试验结果总体一致，没有出现新的安全信号。","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/1396591.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":["LU2417539215.USD","BK4023","AZN","BK4007","LU0320765992.SGD","LU1169590202.USD","LU2456880835.USD","LU1169589451.USD","LU2462157665.USD","PD","LU1829250122.USD","BK4568","LU2236285917.USD","BK4588","BK4585","LU0889565916.HKD","LU0109394709.USD"],"gpt_icon":0},{"id":"2603621919","title":"港股异动 | 维立志博-B(09887)涨超4% PD-L1/4-1BB双抗获FDA快速通道资格","url":"https://stock-news.laohu8.com/highlight/detail?id=2603621919","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603621919?lang=zh_cn&edition=fundamental","pubTime":"2026-01-15 10:02","pubTimestamp":1768442529,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，维立志博-B涨超4%，截至发稿，涨4.26%，报56.3港元，成交额300.03万港元。消息面上，1月14日晚，维立志博宣布，公司自主研发的抗PD-L1/4-1BB双特异性抗体维利信获得美国食品药品监督管理局授予快速通道资格认定，用于治疗肺外神经内分泌癌。这一里程碑将有力推动其全球开发进程，加速药物上市，早日惠及全球患者。","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/1393120.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":["BK1161","PD","BK4023","09887","LU1169589451.USD","HK0000500386.USD","HK0000252152.HKD","LU1169590202.USD","HK0000252160.HKD"],"gpt_icon":0},{"id":"2603612075","title":"维立志博-B(09887)：维利信™(PD-L1/4-1BB双特异性抗体奥帕替苏米单抗，LBL-024)获美国FDA授予快速通道资格认定","url":"https://stock-news.laohu8.com/highlight/detail?id=2603612075","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603612075?lang=zh_cn&edition=fundamental","pubTime":"2026-01-14 22:52","pubTimestamp":1768402376,"startTime":"0","endTime":"0","summary":"智通财经APP讯，维立志博-B 发布公告，于2026年1月14日，PD-L1/4-1BB双特异性抗体维利信TM获美国食品药品监督管理局授予快速通道资格认定，用于治疗肺外神经内分泌癌。快速通道资格认定是FDA批准加速审查治疗严重或危及生命病情或解决未满足医疗需求的药物以助加快药物开发的方法。维利信TM是一种同时靶向PD-L1与4-1BB的双特异性抗体，为针对肺外神经内分泌癌的全球首款达到注册临床阶段的靶向4-1BB受体的疗法。","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/1393010.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":["HK0000252152.HKD","PD","BK4023","HK0000252160.HKD","LU1169589451.USD","BK1161","LU1169590202.USD","09887","HK0000500386.USD"],"gpt_icon":1},{"id":"2603539575","title":"港股异动 | 复宏汉霖(02696)再涨超8% 广谱抗肿瘤PD-L1 ADC HLX43末线食管鳞癌II期数据首次发布","url":"https://stock-news.laohu8.com/highlight/detail?id=2603539575","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603539575?lang=zh_cn&edition=fundamental","pubTime":"2026-01-13 10:12","pubTimestamp":1768270333,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，复宏汉霖再涨超8%，截至发稿，涨8.05%，报69.8港元，成交额1864.08万港元。消息面上，1月9日，复宏汉霖在2026年美国临床肿瘤学会胃肠道肿瘤研讨会上，首度公布了其PD-L1 ADC HLX43治疗复发/转移性食管鳞癌的II期概念验证数据，本次发布的数据初步验证了HLX43在经治的晚期ESCC患者中的治疗潜力，展现出令人鼓舞的疗效及良好的安全性。","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/1392033.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","BK4080","02696","ADC","HK0000165453.HKD","LU1169589451.USD","BK4231","PD","HK0000306701.USD","BK4023","LU1169590202.USD","HK0000320264.USD","HK0000320223.HKD","HK0000306685.HKD"],"gpt_icon":0},{"id":"2603357301","title":"PD-1/VEGF双抗交易热潮回归？荣昌生物签下56亿美元授权","url":"https://stock-news.laohu8.com/highlight/detail?id=2603357301","media":"第一财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603357301?lang=zh_cn&edition=fundamental","pubTime":"2026-01-13 10:03","pubTimestamp":1768269780,"startTime":"0","endTime":"0","summary":"艾伯维拿下荣昌生物的双抗授权。　　1月12日晚间，中国生物医药企业荣昌生物宣布，与艾伯维达成一笔总金额高达56亿美元的授权合作。　　RC148是荣昌生物研发的一款新型靶向PD-1/VEGF的双特异性抗体药物，其设计旨在激活抗肿瘤免疫反应的同时抑制肿瘤驱动的血管生成。通过同时靶向并抑制PD-1与VEGF通路，有望通过多机制增强免疫系统的抗肿瘤活性。　　值得一提的是，康方生物PD-1/VEGF再度传来新的进展消息。","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"sina","url":"https://finance.sina.com.cn/roll/2026-01-13/doc-inhhcntx9294031.shtml","rn_cache_url":null,"customStyle":"body{padding-top:10px;}.art_tit_h1{#titleStyle#}a{#lv2TextColor#}.art_time, .art_cite{#sourceStyle#;} .art_cite{margin-left: 3px;}","selectors":".module-article, article","filters":"header, .voice2, .tags, #norm_qrcode_link_auto, .unfold-box, 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11:18","pubTimestamp":1767842338,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，复宏汉霖盘中涨超5%，截至发稿，涨4.39%，报66.65港元，成交额2390.53万港元。其中，复宏汉霖首次公布其PD-L1 ADC药物HLX43治疗复发/转移性食管鳞状细胞癌中的临床数据。HLX43是靶向PD-L1的新型ADC药物，兼具免疫检查点抑制与细胞毒性双重作用，其I期临床已证实对免疫治疗无效患者具有前景疗效和良好耐受性。本项Ⅱ期研究旨在评估HLX43用于经治复发 / 转移性食管鳞状细胞癌患者的疗效与安全性。","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/1390237.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":["LU1169590202.USD","02696","BK1161","LU1169589451.USD","BK4231","ADC","BK4023","HK0000165453.HKD","PD","BK4080"],"gpt_icon":0},{"id":"2601387879","title":"维亚臻生物VSA012注射液启动II期临床 适应症为活动性狼疮肾炎等疾病","url":"https://stock-news.laohu8.com/highlight/detail?id=2601387879","media":"新浪财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2601387879?lang=zh_cn&edition=fundamental","pubTime":"2026-01-07 18:03","pubTimestamp":1767780180,"startTime":"0","endTime":"0","summary":"药物临床试验登记与信息公示平台数据显示，维亚臻生物技术（苏州）有限公司的评估VSA012注射液在中国活动性狼疮肾炎患者、原发性IgA肾病患者、C3肾小球病患者和免疫复合物介导的膜增生性肾小球肾炎患者中的有效性和安全性的多中心、开放设计的II期临床研究已启动。这些疾病均属肾脏病症，会损害肾功能，引发蛋白尿、血尿等症状，诊断依赖肾活检及相关检验。","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=nesSN20260107185357a6fe6d42&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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1月5日，天士力在互动平台回答投资者提问时表示，根据公司《2025年半年度报告》，PD-L1/VEGF双抗的实体瘤适应症IIa期、直肠癌适应症IIb期临床试验正在入组中；培重组人成纤维细胞生长因子21注射液，临床试验已进入Ib期。后续研发进展公司会根据信息披露相关规定进行公告。（文章来源：证券日报）\n\n\n海量资讯、精准解读，尽在新浪财经APP","market":"sg","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"sina","url":"https://finance.sina.com.cn/stock/relnews/cn/2026-01-05/doc-inhfhpmh6572122.shtml","rn_cache_url":null,"customStyle":"body{padding-top:10px;}.art_tit_h1{#titleStyle#}a{#lv2TextColor#}.art_time, .art_cite{#sourceStyle#;} .art_cite{margin-left: 3px;}","selectors":".module-article, article","filters":"header, .voice2, .tags, #norm_qrcode_link_auto, .unfold-box, 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系晚期pMMR子宫内膜癌唯一医保抗PD-(L)1药物","url":"https://stock-news.laohu8.com/highlight/detail?id=2600089095","media":"中国网财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2600089095?lang=zh_cn&edition=fundamental","pubTime":"2026-01-01 15:16","pubTimestamp":1767251765,"startTime":"0","endTime":"0","summary":"中国网财经1月1日讯今日，北京、上海、苏州、郑州等多地医院开出信迪利单抗注射液(达伯舒)新增子宫内膜癌适应症医保处方，标志着该适应症在被纳入《国家基本医疗保险、生育保险和工伤保险药品目录(2025年)》后正式落地执行医保价格。","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202601013607458241.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202601013607458241.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_eastmoney","symbols":["LU1169589451.USD","BK4585","LU0210528500.USD","PD","BK4588","LU0053666078.USD","BK4023","L","BK4107","LU1169590202.USD","LU2487616109.SGD"],"gpt_icon":0},{"id":"2592795703","title":"【新股IPO】国元国际：瀚思艾泰-B(03378)CD47/PD-1双特异性抗体具备独特性 建议谨慎申购","url":"https://stock-news.laohu8.com/highlight/detail?id=2592795703","media":"金吾财讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2592795703?lang=zh_cn&edition=fundamental","pubTime":"2025-12-17 10:55","pubTimestamp":1765940103,"startTime":"0","endTime":"0","summary":"2023 年5月获FDA批准开展 HX009 Ib/II 期治疗 DLBCL 研究。公司的管线有独特的竞争优势，截至2025年12 月 1 日，全球无已获批的 CD47/PD-1 双特异性抗体产品，HX009在该靶点组合中处于唯一性地位。上市后市值在 38.14-43.59 亿港元，但考虑到公司的 CD47/PD-1 双特异性抗体有一定的独特性，如果上市之后，产品有较大的潜力，建议谨慎申购。","market":"sh","thumbnail":"https://static.szfiu.com/news/20250107/NWEyNjUzNmNkZDE2ZjIxMDg2ODEwOTExNzY3Nw==.png","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20250107/NWEyNjUzNmNkZDE2ZjIxMDg2ODEwOTExNzY3Nw==.png"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"1971704","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":["BK1535","LU1169589451.USD","LU1169590202.USD","BK1173","PD","03378","BK4023"],"gpt_icon":1},{"id":"2591164645","title":"康辰药业(603590.SH)：KC1036联合PD-1抗体和含铂化疗一线治疗晚期复发或转移性食管鳞癌Ⅱ期临床研究完成首例受试者入组","url":"https://stock-news.laohu8.com/highlight/detail?id=2591164645","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2591164645?lang=zh_cn&edition=fundamental","pubTime":"2025-12-15 20:05","pubTimestamp":1765800325,"startTime":"0","endTime":"0","summary":"智通财经APP讯，康辰药业(603590.SH)发布公告，近日，公司自主研发的KC1036片(简称“KC1036”)，顺利完成“KC1036联合PD-1抗体和含铂化疗一线治疗晚期复发或转移性食管鳞癌临床试验(KC1036-COM-01)”首例受试者入组服药。KC1036是公司自主研发的化学药品1类创新药，公司拥有该产品的全球知识产权。KC1036通过抑制VEGFR2、AXL等多靶点实现抗肿瘤活性。KC1036具有较强的VEGFR血管靶向，抑制肿瘤细胞生长;通过抑制AXL，可以改善宿主的抗肿瘤免疫应答，从而避免肿瘤的免疫逃逸。","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/1381753.html","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":"stock_zhitongcaijing","symbols":["LU1169590202.USD","LU1169589451.USD","BK4023","PD","603590","BK0239"],"gpt_icon":0},{"id":"2590504741","title":"产业新闻 | FDA授予百时美施贵宝PD-1疗法组合优先审评资格；创新帕金森病免疫疗法积极试验结果公布","url":"https://stock-news.laohu8.com/highlight/detail?id=2590504741","media":"药明康德","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590504741?lang=zh_cn&edition=fundamental","pubTime":"2025-12-12 08:00","pubTimestamp":1765497601,"startTime":"0","endTime":"0","summary":"FDA授予百时美施贵宝PD-1疗法组合优先审评资格百时美施贵宝今日宣布，美国FDA已受理Opdivo的补充生物制品许可申请，用于与多柔比星、长春花碱和达卡巴嗪联合，治疗既往未接受治疗的III期或IV期经典型霍奇金淋巴瘤成人及儿童患者。FDA授予该申请优先审评资格，并将PDUFA日期确定为2026年4月8日。此次FDA受理及优先审评的决定，主要基于3期SWOG S1826研究的积极结果。","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=nesSN20251212092546a443889e&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, 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| 荣昌生物(09995)盘中涨超7% 公布PD-1/VEGF双抗非小细胞肺癌临床数据","url":"https://stock-news.laohu8.com/highlight/detail?id=2590563981","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590563981?lang=zh_cn&edition=fundamental","pubTime":"2025-12-11 10:45","pubTimestamp":1765421137,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，荣昌生物盘中涨超7%，截至发稿，涨5.57%，报81.5港元，成交额3.1亿港元。会上，由荣昌生物自主研发的PD-1/VEGF双特异性抗体RC148单药及联合方案一线或二线治疗非小细胞肺癌的一项Ⅰ/Ⅱ期临床研究数据，以壁报形式正式发布。据悉，今年8月，RC148已获FDA批准在美国开展II期临床试验。获得FDA的IND许可，标志着该药将进入全球临床开发阶段。","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/1380238.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","LU1169589451.USD","09995","LU2148510915.USD","LU2488822045.USD","BK1574","PD","BK4023","BK0239","BK1583","LU1064130708.USD","LU1969619763.USD","LU2328871848.SGD","LU1169590202.USD","LU1064131003.USD","688331"],"gpt_icon":0},{"id":"2589801094","title":"和誉-B(02256)：和誉医药于ESMO Asia 2025公布口服PD-L1抑制剂ABSK043联合 EGFR抑制剂伏美替尼治疗NSCLC的II期临床初步结果","url":"https://stock-news.laohu8.com/highlight/detail?id=2589801094","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589801094?lang=zh_cn&edition=fundamental","pubTime":"2025-12-08 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科伦博泰与Crescent达成双向授权协议","url":"https://stock-news.laohu8.com/highlight/detail?id=2589289437","media":"每日经济新闻","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589289437?lang=zh_cn&edition=fundamental","pubTime":"2025-12-05 19:52","pubTimestamp":1764935561,"startTime":"0","endTime":"0","summary":"12月4日，科伦博泰（HK06990）与CrescentBiopharma,Inc.（一家纳斯达克上市公司，以下简称Crescent）共同宣布，双方已建立战略合作伙伴关系。科伦博泰方面将ADC药物（抗体偶联药物）SKB105在中国以外权利授权Crescent，并预计将获得最高超13亿美元的授权收入。","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202512053584015760.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202512053584015760.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["PD","BK4023","LU1169590202.USD","ADC","LU1169589451.USD","BK4231","BK4080"],"gpt_icon":0},{"id":"2589865213","title":"ADC与PD-1红海之外，宝济药业如何找到生物医药的“第二增长曲线”？","url":"https://stock-news.laohu8.com/highlight/detail?id=2589865213","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589865213?lang=zh_cn&edition=fundamental","pubTime":"2025-12-05 13:33","pubTimestamp":1764912788,"startTime":"0","endTime":"0","summary":"而在ADC、PD-1等热门靶点赛道数百家企业拥挤厮杀，从临床入组速度到未来的市场定价无不白热化的竞争中，上海宝济药业股份有限公司选择了一条截然不同的差异化战略路径。与传统疗法相比，KJ103的革命性优势则在于其“快”。目前，其领先地位和临床价值已获得监管机构的高度认可。对于KJ017而言，其市场空间并不取决于自身的销量，而是与整个千亿级生物药市场的增长深度绑定，其商业模式堪称典型的“卖水人”逻辑。","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/1378061.html","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":"stock_zhitongcaijing","symbols":["161726","BK4231","ADC","BK4023","PD","399441","02659","LU1169590202.USD","LU1169589451.USD","BK4080"],"gpt_icon":1}],"pageSize":20,"totalPage":4,"pageCount":1,"totalSize":76,"code":"91000000","status":"200"}]}}