688062 迈威生物-U
已收盘 07-21 15:00:01
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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 01:35
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
迈威生物(688062.SH)：注射用6MW5311临床试验申请获得FDA许可
智通财经 · 06-12
迈威生物(688062.SH)：注射用6MW5311临床试验申请获得FDA许可
每周股票复盘：迈威生物（688062）召开两次临时股东会
证券之星 · 06-07
每周股票复盘：迈威生物（688062）召开两次临时股东会
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 · 06-04
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国家药监局批准
美股速递 · 06-04
迈威生物-U：9MW5211注射液临床试验申请获国家药监局批准
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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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01:35","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":"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/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":["688062","02493","BK1161","BK0239"],"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.laohu8.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.laohu8.com/m/news/2650115423?lang=zh_cn&edition=full","pubTime":"2026-07-12 02:49","pubTimestamp":1783795748,"startTime":"0","endTime":"0","summary":"截至2026年7月10日收盘，迈威生物报收于31.87元，较上周的32.06元下跌0.59%。本周关注点公司公告汇总：9MW5211注射液用于1型糖尿病适应症的临床试验申请获国家药监局批准公司公告汇总：该药品此前已获批用于炎症性肠病和多发性硬化适应症的临床试验公司公告汇总：9MW5211注射液针对多种自身免疫性疾病核心病理机制，具高度特异性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。","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/RB2026071200000973.shtml","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":"stockstar","symbols":["688062","02493","BK1161","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1198547368","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=1198547368","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1198547368?lang=zh_cn&edition=full","pubTime":"2026-07-07 21:16","pubTimestamp":1783430197,"startTime":"0","endTime":"0","summary":"迈威生物-U (688062) 宣布，其研发的9MW5211注射液临床试验申请已获得中国国家药品监督管理局的正式批准。\n这一进展标志着该创新药物将进入临床开发阶段，为后续的疗效与安全性评估铺平了道路。公司致力于推进其生物制药产品管线，此次获批是其研发进程中的重要里程碑。","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":["688062","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2649987609","title":"迈威生物(688062.SH)：9MW5211注射液临床试验申请获批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2649987609","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2649987609?lang=zh_cn&edition=full","pubTime":"2026-07-07 20:15","pubTimestamp":1783426507,"startTime":"0","endTime":"0","summary":"智通财经APP讯，迈威生物 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》，9MW5211注射液用于1型糖尿病适应症的临床试验申请获得批准，此前，其用于炎症性肠病适应症的临床试验申请已分别获得国家药品监督管理局批准和FDA许可，用于多发性硬化适应症的临床试验申请已获得国家药品监督管理局批准。通过选择性识别并清除这群致病性细胞，9MW5211可有效阻断免疫级联反应，进而缓解疾病进展并改善临床症状。","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/1464336.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":["688062","IBBQ","BMED","02493","BK0239","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2649079984","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=2649079984","media":"格隆汇","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2649079984?lang=zh_cn&edition=full","pubTime":"2026-07-07 19:36","pubTimestamp":1783424169,"startTime":"0","endTime":"0","summary":null,"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://www.gelonghui.com/rss/live/live.xml","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":"live_gelonghui","symbols":["688062","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2648963169","title":"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%","url":"https://stock-news.laohu8.com/highlight/detail?id=2648963169","media":"证券之星","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2648963169?lang=zh_cn&edition=full","pubTime":"2026-07-03 08:02","pubTimestamp":1783036924,"startTime":"0","endTime":"0","summary":"证券之星消息，根据市场公开信息整理，迈威生物于7月3日将有2607.0万股限售股份解禁，为公司追加承诺限售股份上市流通，占公司总股本5.84%。本次解禁后，公司还有1.69亿股限售股份，占总股本37.91%。本文数据来源于迈威生物公告，仅供参考不构成投资建议。","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/RB2026070300008547.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":"stockstar","symbols":["BK0239","688062","BK1161","02493"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2646646809","title":"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%","url":"https://stock-news.laohu8.com/highlight/detail?id=2646646809","media":"证券之星","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2646646809?lang=zh_cn&edition=full","pubTime":"2026-06-25 22:27","pubTimestamp":1782397637,"startTime":"0","endTime":"0","summary":"截至2026年6月25日收盘，迈威生物报收于27.72元，较前一交易日上涨0.14%，最新总市值为123.83亿元。近日，迈威（上海）生物科技股份有限公司发布《首次公开发行部分限售股上市流通公告》。公告显示，公司首次公开发行部分限售股将于2026年7月3日上市流通，本次上市流通数量为26,070,000股，占公司A股股本的6.52%，占总股本的5.84%。上述股东已履行相关承诺，保荐机构对本次限售股上市流通无异议。","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/RB2026062500044214.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":["BK0239","688062","BK1161","02493"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1100490246","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=1100490246","media":"投资观察","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1100490246?lang=zh_cn&edition=full","pubTime":"2026-06-23 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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":["BK0239","BK1161","02493","688062"],"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.laohu8.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","02493","BK1161","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.laohu8.com/m/news/1143771369?lang=zh_cn&edition=full","pubTime":"2026-06-19 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