688062 迈威生物-U
盘后交易 08-12 15:00:01
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港股午评|恒生指数早盘跌0.63% CRO概念继续走高
智通财经 · 08-11 12:00
港股午评|恒生指数早盘跌0.63% CRO概念继续走高
每周股票复盘：迈威生物（688062）9MW5211注射液获临床试验批准
证券之星 · 08-02
每周股票复盘：迈威生物（688062）9MW5211注射液获临床试验批准
迈威生物-U：9MW5211注射液临床试验申请获国家药监局批准
投资观察 · 07-31
迈威生物-U：9MW5211注射液临床试验申请获国家药监局批准
迈威生物-U：9MW5211注射液临床试验申请获NMPA批准
美股速递 · 07-31
迈威生物-U：9MW5211注射液临床试验申请获NMPA批准
每周股票复盘：迈威生物（688062）9MW5211注射液获准开展白癜风临床试验
证券之星 · 07-19
每周股票复盘：迈威生物（688062）9MW5211注射液获准开展白癜风临床试验
迈威生物-U新药9MW5211注射液临床试验申请获国家药监局批准
美股速递 · 07-15
迈威生物-U新药9MW5211注射液临床试验申请获国家药监局批准
每周股票复盘：迈威生物（688062）9MW5211注射液获批T1DM临床试验
证券之星 · 07-12
每周股票复盘：迈威生物（688062）9MW5211注射液获批T1DM临床试验
迈威生物-U新药9MW5211注射液临床试验申请获国家药监局批准
美股速递 · 07-07
迈威生物-U新药9MW5211注射液临床试验申请获国家药监局批准
迈威生物(688062.SH)：9MW5211注射液临床试验申请获批准
智通财经 · 07-07
迈威生物(688062.SH)：9MW5211注射液临床试验申请获批准
迈威生物：9MW5211注射液获国家药监局批准开展1型糖尿病临床试验
格隆汇 · 07-07
迈威生物：9MW5211注射液获国家药监局批准开展1型糖尿病临床试验
迈威生物（688062）2607万股限售股将于7月3日解禁，占总股本5.84%
证券之星 · 07-03
迈威生物（688062）2607万股限售股将于7月3日解禁，占总股本5.84%
迈威生物（688062）披露首次公开发行部分限售股上市流通公告，6月25日股价上涨0.14%
证券之星 · 06-25
迈威生物（688062）披露首次公开发行部分限售股上市流通公告，6月25日股价上涨0.14%
迈威生物-U获国家药监局批准开展6MW5311注射液临床试验申请
投资观察 · 06-23
迈威生物-U获国家药监局批准开展6MW5311注射液临床试验申请
迈威生物(688062.SH)：注射用6MW5311临床试验申请获国家药监局批准
智通财经 · 06-23
迈威生物(688062.SH)：注射用6MW5311临床试验申请获国家药监局批准
迈威生物（688062）披露召开2025年度暨2026年第一季度业绩说明会公告，6月22日股价下跌1.24%
证券之星 · 06-22
迈威生物（688062）披露召开2025年度暨2026年第一季度业绩说明会公告，6月22日股价下跌1.24%
每周股票复盘：迈威生物（688062）9MW2821临床数据亮相ESMO Gynae
证券之星 · 06-20
每周股票复盘：迈威生物（688062）9MW2821临床数据亮相ESMO Gynae
迈威生物宣布胡慧国将卸任执行董事
投资观察 · 06-19
迈威生物宣布胡慧国将卸任执行董事
迈威生物第三届董事会选举唐春山、刘大涛、吴海、华军为执行董事 决议现已生效
美股速递 · 06-18
迈威生物第三届董事会选举唐春山、刘大涛、吴海、华军为执行董事 决议现已生效
迈威生物-U（688062）6MW5311临床试验申请获国家药监局受理审评
美股速递 · 06-12
迈威生物-U（688062）6MW5311临床试验申请获国家药监局受理审评
迈威生物-U获美国FDA批准开展临床试验
美股速递 · 06-12
迈威生物-U获美国FDA批准开展临床试验
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公司概况
公司名称：
迈威(上海)生物科技股份有限公司
所属行业：
医药制造业
上市日期：
2022-01-18
主营业务：
迈威(上海)生物科技股份有限公司的主营业务是研发、生产以及销售创新型药物和生物类似药。公司的主要产品是抗体、ADC药物和重组蛋白、小分子化学药等药物。
发行价格：
34.80
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01:46","pubTimestamp":1785606376,"startTime":"0","endTime":"0","summary":"截至2026年7月31日收盘，迈威生物报收于28.68元，较上周的31.09元下跌7.75%。本周，迈威生物7月27日盘中最高价报32.64元。迈威生物当前最新总市值128.12亿元，在化学制药板块市值排名35/149，在两市A股市值排名1397/5202。公司公告汇总迈威生物自愿披露关于9MW5211注射液临床试验申请获得国家药品监督管理局批准的公告。9MW5211注射液用于原发性胆汁性胆管炎适应症的临床试验申请已获批准。","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":"https://stock.stockstar.com/RB2026080200000348.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":"stockstar","symbols":["BK0239","BK1161","02493","688062"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1132577846","title":"迈威生物-U：9MW5211注射液临床试验申请获国家药监局批准","url":"https://stock-news.laohu8.com/highlight/detail?id=1132577846","media":"投资观察","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1132577846?lang=zh_cn&edition=full","pubTime":"2026-07-31 20:36","pubTimestamp":1785501414,"startTime":"0","endTime":"0","summary":"北京时间7月31日消息——迈威生物（上海）生物科技股份有限公司（688062.SS）正式对外披露，其自主研发的9MW5211注射液已获得国家药品监督管理局（NMPA）的临床试验申请批准。这一进展标志着该候选药物正式迈入临床试验阶段，有望为相关疾病领域带来新的治疗选择。\n","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK0239","688062"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1103867558","title":"迈威生物-U：9MW5211注射液临床试验申请获NMPA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=1103867558","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1103867558?lang=zh_cn&edition=full","pubTime":"2026-07-31 20:12","pubTimestamp":1785499955,"startTime":"0","endTime":"0","summary":"迈威生物（上海）生物科技股份有限公司宣布，其研发的9MW5211注射液已获得国家药品监督管理局（NMPA）的临床试验批准通知书。这一进展标志着该候选药物正式进入临床开发阶段，为后续研究铺平了道路。","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":["688062","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2652237484","title":"每周股票复盘：迈威生物（688062）9MW5211注射液获准开展白癜风临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2652237484","media":"证券之星","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2652237484?lang=zh_cn&edition=full","pubTime":"2026-07-19 01:35","pubTimestamp":1784396110,"startTime":"0","endTime":"0","summary":"截至2026年7月17日收盘，迈威生物报收于31.0元，较上周的31.87元下跌2.73%。本周，迈威生物7月16日盘中最高价报36.0元。此前，该药品用于炎症性肠病、多发性硬化和1型糖尿病适应症的临床试验申请已获国家药监局批准，其中IBD适应症还获得FDA许可。9MW5211为全球首个靶向该分子的临床阶段候选药物，临床前研究显示其在多种自身免疫疾病模型中具有显著治疗潜力，且安全性良好。","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":"https://stock.stockstar.com/RB2026071900000285.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":"stockstar","symbols":["BK1161","BK0239","02493","688062"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1123562061","title":"迈威生物-U新药9MW5211注射液临床试验申请获国家药监局批准","url":"https://stock-news.laohu8.com/highlight/detail?id=1123562061","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1123562061?lang=zh_cn&edition=full","pubTime":"2026-07-15 20:03","pubTimestamp":1784117023,"startTime":"0","endTime":"0","summary":"迈威生物（上海）股份有限公司宣布，其研发的9MW5211注射液的临床试验申请，已正式获得国家药品监督管理局的批准。\n这一进展标志着公司的一款在研新药向临床开发阶段迈出了关键一步。9MW5211注射液是迈威生物管线中的重要候选药物，其获批开展临床试验，为后续的研发进程奠定了基础。\n公司后续将按照国家相关法律法规和要求，积极开展该药物的临床试验工作。","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":["688062","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2650115423","title":"每周股票复盘：迈威生物（688062）9MW5211注射液获批T1DM临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2650115423","media":"证券之星","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2650115423?lang=zh_cn&edition=full","pubTime":"2026-07-12 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18:37","pubTimestamp":1782211020,"startTime":"0","endTime":"0","summary":"智通财经APP讯，迈威生物(688062.SH)发布公告，近日，公司收到国家药品监督管理局核准签发的《药物临床试验批准通知书》，注射用6MW5311用于血液瘤(急性髓系白血病(AML)、慢性粒单核细胞白血病(CMML)以及多发性骨髓瘤(MM))适应症的临床试验申请获得批准。6MW5311是基于公司T Cell Engager(TCE)技术平台开发的一款靶向LILRB4/CD3的双特异性抗体，拟开发适应症为：血液瘤(AML、CMML以及MM)。","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/1457612.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","688062","02493","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2645073615","title":"迈威生物（688062）披露召开2025年度暨2026年第一季度业绩说明会公告，6月22日股价下跌1.24%","url":"https://stock-news.laohu8.com/highlight/detail?id=2645073615","media":"证券之星","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2645073615?lang=zh_cn&edition=full","pubTime":"2026-06-22 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Gynae以口头报告形式公布宫颈癌临床数据。职工代表大会选举桂勋先生为第三届董事会职工代表董事，其任期自非职工代表董事就任之日起至本届董事会任期届满。迈威生物在2026年欧洲肿瘤内科学会妇科肿瘤年会上以口头报告和壁报形式公布9MW2821治疗复发性或转移性宫颈癌的最新临床数据。","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://stock.stockstar.com/RB2026062000002013.shtml","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":"stockstar","symbols":["688062","BK1161","02493","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1143771369","title":"迈威生物宣布胡慧国将卸任执行董事","url":"https://stock-news.laohu8.com/highlight/detail?id=1143771369","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1143771369?lang=zh_cn&edition=full","pubTime":"2026-06-19 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