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49.76

+0.85001.74%

盘后：49.760.00000.00%16:05 EDT

成交量：1.71万

成交额：85.43万

市值：16.75亿

市盈率：20.65

高：51.08

开：49.27

低：48.92

收：48.91

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总览公司新闻公告

GLP-1降糖药深陷“视力门”：风险几何？机制何解？诺和诺德回应了

21世纪经济报道

诺和诺德回应降糖版司美格鲁肽或致失明：确诊病例非常少不存在不利于公司GLP-1类产品的失衡问题

诺和诺德回应降糖版司美格鲁肽或致失明：确诊病例非常少，不存在不利于公司GLP-1类产品的失衡问题

人源超长效GLP-1降糖减重新药上市阿里健康大药房线上首发

四川双马：司美格鲁肽原料药价格逐步回落是必然公司有较充分应对空间

江海证券：糖尿病新药怡诺轻开出全国首张处方建议关注GLP-1类药物产业链相关企业

上海自研GLP-1糖尿病新药开出首张处方，或将挑战司美格鲁肽

GLP-1“带飞”，礼来业绩大增

国际金融报

新股解读|派格生物：不足三年亏损近8亿元核心GLP-1单品能否上演造富神话？

MNC年报扫描｜“明星”产品替尔泊肽营收大增礼来能否在GLP-1竞赛中称霸？

21世纪经济报道

【众生药业：控股子公司RAY1225注射液获美国FDA临床试验批准，针对超重或肥胖适应症开展II期试验】金融界2月7日消息，近日，众生药业控股子公司众生睿创自主研发的一类创新多肽药物RAY1225注射液收到美国FDA签发的药物临床试验批准通知书，同意其直接在美国开展超重或肥胖适应症的II期临床试验。RAY1225注射液是具有全球自主知识产权的创新结构多肽药物，属于长效GLP-1类药物，有GLP-1受体和GIP受体双重激动活性。RAY1225注射液治疗中国肥胖/超重患者与2型糖尿病患者的两项II期临床研究的较高剂量递增和扩展研究部分仍在进行中。众生睿创于2024年12月向FDA递交相关数据申请，并于近日获得批准。根据规定，该注射液获得在美临床试验资格后，尚需开展临床试验并经审批通过方可上市销售，对公司短期财务和经营业绩不构成重大影响，对公司业绩产生影响的时间不确定。

礼来公布2024年业绩，GLP-1大卖200多亿美元

【博济医药：通过GLP认证复查并获得《药物GLP认证证书》】博济医药公告，公司近日收到国家药品监督管理局颁发新的《药物GLP认证证书》，编号为GLP039010219。公司顺利通过GLP认证复查，并获得了《药物GLP认证证书》，共8项认证资质。具体开展药物非临床安全性评价研究的机构名称为博济医药科技股份有限公司药物评价中心，机构地址为广州黄埔区科学城南翔一路62号（二、三、四、五）栋。试验项目包括单次和重复给药毒性试验、生殖毒性试验、遗传毒性试验、局部毒性试验、免疫原性试验、安全药理学试验、毒代动力学试验。认证结论为公司符合药物非临床研究质量管理规范的要求，有效期至2030年1月22日。本次通过GLP认证复查，有利于公司对外承接药物非临床安全性评价业务，持续巩固公司为客户提供新药研发一站式服务的能力。

Global Partners盘中异动大幅上涨5.00%

美国总统特朗普的卫生部长提名人小肯尼迪：支持为患有重度肥胖和糖尿病的成年人开具GLP药物处方，但前提是结合锻炼。

市场消息：美国食品药品监督管理局（FDA）批准Ozempic作为唯一一种GLP-1受体激动剂，以降低2型糖尿病和慢性肾病

【国家药监局批准依苏帕格鲁肽α注射液上市】近日，国家药品监督管理局批准上海银诺医药技术有限公司申报的依苏帕格鲁肽α注射液（商品名：怡诺轻）上市。适用于成人2型糖尿病患者的血糖控制。依苏帕格鲁肽α注射液是一种长效胰高血糖素样肽-1受体激动剂（GLP-1RA），是人胰高血糖素样肽-1（GLP-1）与人免疫球蛋白G2（IgG2）的Fc片段融合形成的重组蛋白，可以血糖依赖性地增加胰岛素分泌，抑制胰高血糖素释放，用于2型糖尿病的治疗。该品种的上市为相关患者提供了新的治疗选择。

经济日报刊评：减肥药要慎用

【经济日报刊评：减肥药要慎用】日前，口服司美格鲁肽片获国家药监局批准在中国全面上市，这是目前国内首个且唯一获批上市的口服GLP-1药物。记者在采访中了解到，近日前往医院咨询这款口服司美格鲁肽的患者增多，其中一些患者希望可以通过这款药物实现减重。“无论是司美格鲁肽注射液还是口服制剂都会有一些副作用，最常见的不良反应为恶心、腹泻、呕吐、胃食管反流病和2型糖尿病患者低血糖。有消化系统疾病、甲状腺癌疾病史或家族史等人群使用该药物有风险。”专家提醒，司美格鲁肽需要在医生指导下合理用药，切勿自行在网上购买使用。

【研究：流行减重药获益与风险共存】最新一期《自然·医学》杂志发表了一项观察性研究，科学家对使用胰高血糖素样肽1受体激动剂的健康影响进行了分析，结论是42种健康风险下降以及19种健康风险上升。 GLP-1RA在过去几年里因宣称具有减重效果而广为流行。人们也在研究GLP-1RA的更广泛疗效，包括治疗阿尔茨海默病、骨关节炎和睡眠呼吸暂停等疾病。但一些不良事件如自杀倾向和胃肠道问题也有所报道。因此有必要进一步研究GLP-1RA的健康获益和风险。

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15:20","pubTimestamp":1739431238,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，江海证券发布研报称，上海银诺医药技术有限公司自主研发的糖尿病新药怡诺轻正式获批上市，并开出全国首张处方。随着国内糖尿病患者增多、政策大力扶持，相关创新药市场潜力巨大，建议关注GLP-1类药物研发等相关企业，随着国内政策不断加码，以及中国创新药企业的积极应对，中国药企相关创新药的不断上市将会挑战司美格鲁肽产品的全球地位。","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/1249324.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":["02196","GLP","BK1191","161027","BK1593","BK1515","BK4144","BK4590"],"gpt_icon":0},{"id":"2510821844","title":"上海自研GLP-1糖尿病新药开出首张处方，或将挑战司美格鲁肽","url":"https://stock-news.laohu8.com/highlight/detail?id=2510821844","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2510821844?lang=zh_cn&edition=fundamental","pubTime":"2025-02-11 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20:06","pubTimestamp":1739189216,"startTime":"0","endTime":"0","summary":"近日，跨国药企礼来发布2024年财报。GLP-1“带飞”第四季度业绩单从第四季度数据来看，礼来实现营收135.33亿美元，同比增长45%；净利润实现翻倍达44.1亿美元。截至目前，礼来共有两款GLP-1/GIP双重激动剂获批上市，分别为降糖版Mounjaro和减重版Zepbound。公司披露的数据显示，截至今年2月4日，礼来共有70余条临床在研管线，分布在糖尿病、肿瘤、免疫、神经四大疾病领域。礼来在2025年业绩指引称，公司预计今年收入将在580亿至610亿美元之间。","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=nesSN20250210200729961ddf06&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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核心GLP-1单品能否上演造富神话？","url":"https://stock-news.laohu8.com/highlight/detail?id=2510027834","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2510027834?lang=zh_cn&edition=fundamental","pubTime":"2025-02-10 18:14","pubTimestamp":1739182468,"startTime":"0","endTime":"0","summary":"派格生物预计，PB-119一旦被纳入国家医保药品目录，其定价将更接近公司的定价估算的下限。换句话说，于往绩记录期间内及截至最后实际可行日期，派格生物没有任何商业化产品。截至2024年9月30日，派格生物持有的现金及现金等价物为2744万元，上年同期为2.19亿元，可发现，派格生物的资金链面临着断裂危险。派格生物之所以获得众多机构投资，与火热GLP-1赛道不无关系。","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/1247897.html","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":"stock_zhitongcaijing","symbols":["BK4144","GLP","BK4590"],"gpt_icon":1},{"id":"2509712618","title":"MNC年报扫描｜“明星”产品替尔泊肽营收大增 礼来能否在GLP-1竞赛中称霸？","url":"https://stock-news.laohu8.com/highlight/detail?id=2509712618","media":"21世纪经济报道","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509712618?lang=zh_cn&edition=fundamental","pubTime":"2025-02-07 19:53","pubTimestamp":1738929196,"startTime":"0","endTime":"0","summary":"2月6日，礼来发布2024年第四季度及全年业绩报告。报告显示，2024年第四季度营收为135.3亿美元，同比增长45%；净利润为44.1亿美元，同比增长101%。2024年全年营收为450.4亿美元，同比增长32%；净利润为105.9亿美元，同比增长102%。从具体的产品看，礼来的“明星”产品替尔泊肽推动了其收入的增长。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202502073313656993.html","rn_cache_url":null,"directOrigin":true},"property":["earning"],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202502073313656993.html","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":"stock_eastmoney","symbols":["GLP","LLY"],"gpt_icon":1},{"id":"2509716421","title":"【众生药业：控股子公司RAY1225注射液获美国FDA临床试验批准，针对超重或肥胖适应症开展II期试验】金融界2月7日消息，近日，众生药业控股子公司众生睿创自主研发的一类创新多肽药物RAY1225注射液收到美国FDA签发的药物临床试验批准通知书，同意其直接在美国开展超重或肥胖适应症的II期临床试验。RAY1225注射液是具有全球自主知识产权的创新结构多肽药物，属于长效GLP-1类药物，有GLP-1受体和GIP受体双重激动活性。RAY1225注射液治疗中国肥胖/超重患者与2型糖尿病患者的两项II期临床研究的较高剂量递增和扩展研究部分仍在进行中。众生睿创于2024年12月向FDA递交相关数据申请，并于近日获得批准。根据规定，该注射液获得在美临床试验资格后，尚需开展临床试验并经审批通过方可上市销售，对公司短期财务和经营业绩不构成重大影响，对公司业绩产生影响的时间不确定。","url":"https://stock-news.laohu8.com/highlight/detail?id=2509716421","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509716421?lang=zh_cn&edition=fundamental","pubTime":"2025-02-07 18:51","pubTimestamp":1738925508,"startTime":"0","endTime":"0","summary":"金融界2月7日消息，近日，众生药业控股子公司众生睿创自主研发的一类创新多肽药物RAY1225注射液收到美国FDA签发的药物临床试验批准通知书，同意其直接在美国开展超重或肥胖适应症的II期临床试验。RAY1225注射液治疗中国肥胖/超重患者与2型糖尿病患者的两项II期临床研究的较高剂量递增和扩展研究部分仍在进行中。众生睿创于2024年12月向FDA递交相关数据申请，并于近日获得批准。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://24h.jrj.com.cn/2025/02/07185148019793.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":"jinrongjie_stock","symbols":["002317","03347","BK4144","BK0239","BK1583","BK4590","GLP","BK1141","BK1576","BK0188","BK0077"],"gpt_icon":0},{"id":"2509787608","title":"礼来公布2024年业绩，GLP-1大卖200多亿美元","url":"https://stock-news.laohu8.com/highlight/detail?id=2509787608","media":"药事纵横","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509787608?lang=zh_cn&edition=fundamental","pubTime":"2025-02-07 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18:53","pubTimestamp":1738752829,"startTime":"0","endTime":"0","summary":"公司顺利通过GLP认证复查，并获得了《药物GLP认证证书》，共8项认证资质。具体开展药物非临床安全性评价研究的机构名称为博济医药科技股份有限公司药物评价中心，机构地址为广州黄埔区科学城南翔一路62号栋。认证结论为公司符合药物非临床研究质量管理规范的要求，有效期至2030年1月22日。本次通过GLP认证复查，有利于公司对外承接药物非临床安全性评价业务，持续巩固公司为客户提供新药研发一站式服务的能力。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://24h.jrj.com.cn/2025/02/05185347963848.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":"jinrongjie_stock","symbols":["BK0216","BK4590","BK4144","GLP","300404"],"gpt_icon":0},{"id":"2507438608","title":"Global Partners盘中异动 大幅上涨5.00%","url":"https://stock-news.laohu8.com/highlight/detail?id=2507438608","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2507438608?lang=zh_cn&edition=fundamental","pubTime":"2025-01-31 05:02","pubTimestamp":1738270933,"startTime":"0","endTime":"0","summary":"北京时间2025年01月31日05时02分，Global Partners股票出现异动，股价急速上涨5.00%。Global Partners股票所在的油气中游产业行业中，整体涨幅为1.19%。其相关个股中，Pyxis Tankers Inc C/Wts 13/10/2025 、Genesis Energy, L.P.、Global Partners涨幅较大，Enlink Midstream, Llc、Plains All American Pipeline, L.P.、International Seaways, Inc.较为活跃，换手率分别为5.07%、1.80%、1.58%，振幅较大的相关个股有Venture Global, Inc.、Global Partners、Genesis Energy, L.P.，振幅分别为10.48%、9.32%、7.45%。Global Partners公司简介：Global Partners 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