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美股
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本页面由Tiger Fintech (Singapore) Pte. Ltd.提供服务
Global Partners Lp
53.11
+0.1100
0.21%
成交量:
2.62万
成交额:
139.06万
市值:
18.06亿
市盈率:
20.42
高:
53.25
开:
52.99
低:
52.26
收:
53.00
52周最高:
60.00
52周最低:
40.66
股本:
3,399.56万
流通股本:
2,767.42万
量比:
0.37
换手率:
0.09%
股息:
2.97
股息率:
5.59%
每股收益(TTM):
2.60
每股收益(LYR):
2.45
净资产收益率:
16.33%
总资产收益率:
4.09%
市净率:
2.96
市盈率(LYR):
21.71
数据加载中...
总览
公司
新闻
公告
歌礼制药-B(01672)将在第61届欧洲糖尿病研究协会(EASD)年会上报告ASC30 口服小分子GLP-1R激动剂28天多剂量递增研究结果
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减重赛道全球前沿进展跟踪(二):ORFORGLIPRON领跑全球小分子GLP-1RA赛道 国内管线价值逐渐凸显
开源证券
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19小时前
司美格鲁肽最新临床数据出炉!GLP-1战火延伸至心血管赛道
21世纪经济报道
·
昨天
在GLP-1(胰高血糖素样肽-1)减肥药的竞争中诺和诺德的司美格鲁肽终于凭借心血管方面的获益扳回一局。9月1日记者从诺和
智通财经
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昨天
礼来终止2项口服GLP-1药二期试验
生物药大时代
·
昨天
礼来口服GLP-1药物orforglipron III期研究成功
药事纵横
·
08/28
谁在网购减重版GLP-1?京东健康:90后购买量排第一,未来电商渠道预计超过七成
时代财经
·
08/27
映恩生物上半年调整后利润1.46亿元,现金37.47亿元;礼来口服GLP-1一项3期临床成功
Ofweek维科网
·
08/27
Viking Therapeutics股价下跌3.8%竞争对手礼来的GLP - 1药片在糖尿病患者后期研究中助力减轻体重
智通财经
·
08/26
礼来公司(Eli Lilly)在晚期试验中发现其GLP - 1片剂使2型糖尿病患者体重减轻10.5%该公司股价上涨3.2
智通财经
·
08/26
礼来公布口服GLP-1RA III期临床结果,肥胖适应症预计今年在美提交
时代财经
·
08/26
礼来公司周二表示其每日服用的减肥药丸在后期试验中帮助肥胖和2型糖尿病患者减轻了体重达到了研究的主要目标为该公司在全球范围
智通财经
·
08/26
浙商证券:看好国内细分领域布局药企出海BD机遇 关注GLP-1多靶点国内一梯队BD进展
智通财经
·
08/26
信达生物小分子GLP-1R激动剂获批临床|亚盛医药Bcl-2抑制剂欧美获批全球注册3期临床|荣昌生物再破局
中国医药创新促...
·
08/25
信达生物小分子GLP-1R激动剂在中国获批临床
药渡
·
08/24
贝莱德的 Levy-Odom 将领导美洲地区的监管工作
路透中文
·
08/23
贝莱德的 Levy-Odom 将领导美洲地区的监管工作
路透中文
·
08/23
研报掘金丨开源证券:华东医药创新药收入快速增长,维持“买入”评级
格隆汇
·
08/21
总数跌破70万家,零售药店上演“鱿鱼游戏”!有门店下场做药妆、开卖GLP-1减肥药
时代财经
·
08/21
更多
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14:14","pubTimestamp":1756275278,"startTime":"0","endTime":"0","summary":"8月26日,映恩生物公告,上半年总营收12.29亿元,调整后利润1.46亿元,现金总额达到37.47亿元。康诺亚也是在同一天宣布,上半年营收4.99亿元,同比暴增812%,其中包括合作收入3.29亿元。研发支出3.60亿元,同比增长9%。礼来口服GLP-1一项3期临床成功。8月26日,礼来公布了其在研GLP-1受体激动剂orforglipron的3期临床试验ATTAIN-2的积极顶线结果。2)复星医药上半年净利润同比增长38.96%8月26日,复星医药公告,2025年上半年营业收入195.14亿元,净利润17.02亿元,同比增长38.96%。","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=nesSN2025082714144297641811&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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Lilly)在晚期试验中发现其GLP - 1片剂使2型糖尿病患者体重减轻10.5%该公司股价上涨3.2","url":"https://stock-news.laohu8.com/highlight/detail?id=2562734322","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2562734322?lang=zh_cn&edition=fundamental","pubTime":"2025-08-26 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III期临床结果,肥胖适应症预计今年在美提交","url":"https://stock-news.laohu8.com/highlight/detail?id=2562851736","media":"时代财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2562851736?lang=zh_cn&edition=fundamental","pubTime":"2025-08-26 20:06","pubTimestamp":1756209973,"startTime":"0","endTime":"0","summary":"本文来源:时代财经8月26日晚间,时代财经获悉,礼来制药公布了每日一次口服小分子GLP-1受体激动剂orforglipron的III期临床试验ATTAIN-2的积极顶线结果。据悉,礼来计划于2025年向美国食品药品管理局提交 orforglipron用于肥胖症治疗的上市许可申请,并于2026年初针对糖尿病治疗启动申报流程。此外,礼来全球高级副总裁、礼来中国药物开发及医学事务中心负责人王莉博士表示,中国已同步加入了orforglipron的全球研发,期待 orforglipron 能早日在中国获批,为中国患者带来新的治疗选择。","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=nesSN2025082620085194fde36f&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description 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19:58","pubTimestamp":1756209527,"startTime":"0","endTime":"0","summary":null,"market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"1562215406f683d19f5eb2345c8cc126","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.zhitongcaijing.com/immediately.html?type=usstock","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_zhitongcaijing","symbols":["LU1804176565.USD","LU1720051017.SGD","LU0203201768.USD","IE00BJLML261.HKD","LU1093756325.SGD","LU2237443465.HKD","LU2237443895.HKD","SGXZ51526630.SGD","LU2106854487.HKD","LU0323591593.USD","LU0820561909.HKD","LU1551013342.USD","LU2108987350.USD","LU1868837136.USD","LU2750360641.GBP","LU1917777945.USD","LU2063271972.USD","LU0079474960.USD","SG9999015986.USD","LU0096364046.USD","SGXZ57979304.SGD","LU0823434740.USD","BK4581","LU2491050154.USD","IE00BK4W5M84.HKD","SG9999014880.SGD","GLP","LU2237443622.USD","LU0234572021.USD","LU0889565916.HKD","LU0471298694.HKD","LU0466842654.USD","BK4144","LU0456855351.SGD","LU0256863811.USD","LU1868837300.USD","NVO","BK4590","LU1057294990.SGD","LU0316494557.USD","LLY","LU0820561818.USD","LU2491049909.HKD","LU0882574055.USD","LU2360106947.USD","LU0320765059.SGD","LU0061475181.USD","LU0097036916.USD","LU0354030511.USD","LU0672654240.SGD"],"gpt_icon":0},{"id":"2562205808","title":"浙商证券:看好国内细分领域布局药企出海BD机遇 关注GLP-1多靶点国内一梯队BD进展","url":"https://stock-news.laohu8.com/highlight/detail?id=2562205808","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2562205808?lang=zh_cn&edition=fundamental","pubTime":"2025-08-26 11:15","pubTimestamp":1756178124,"startTime":"0","endTime":"0","summary":"浙商证券主要观点如下:一、从MNC的GLP-1布局梳理看BD机会全球GLP-1药物市场由诺和诺德和礼来主导,其他MNC正在加速布局中。同时,上述部分MNC在GLP-1领域的技术路径、新靶点、新适应症等方面的布局仍有较大提升空间,该行看好国内细分领域布局药企出海BD机遇。GLP-1多靶点:全球进度靠前,关注国内一梯队BD进展。","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/1335094.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":["BK0276","BK4144","BK4590","601878","GLP"],"gpt_icon":0},{"id":"2562249689","title":"信达生物小分子GLP-1R激动剂获批临床|亚盛医药Bcl-2抑制剂欧美获批全球注册3期临床|荣昌生物再破局","url":"https://stock-news.laohu8.com/highlight/detail?id=2562249689","media":"中国医药创新促...","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2562249689?lang=zh_cn&edition=fundamental","pubTime":"2025-08-25 16:22","pubTimestamp":1756110166,"startTime":"0","endTime":"0","summary":"信达生物 IBI30328月18日,信达生物申报的1类新药IBI3032获得临床试验默示许可,拟用于成人超重或肥胖患者的长期体重控制。8月21日,泽璟制药宣布,其注射用ZG005、注射用ZGGS18与盐酸吉卡昔替尼片联合用于晚期实体瘤的临床试验获得NMPA批准。8月19日,复宏汉霖宣布与启德医药达成战略合作。8月22日,思路迪医药已与楷拓生物签署战略合作协议。","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=nesSN20250825162811a6f9f675&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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07:30","pubTimestamp":1755991846,"startTime":"0","endTime":"0","summary":"中国国家药监局药品审评中心官网近日公示,信达生物申报的1类新药IBI3032获得临床试验默示许可,拟用于成人超重或肥胖患者的长期体重控制。公开资料显示,这是信达生物研发的创新口服小分子GLP-1R激动剂,已经于今年8月初在美国获批IND。作为其自主研发的口服小分子GLP-1药物,IBI3032在临床前动物模型中展现了令人期待的特质,其消除半衰期更长,在相同剂量下的药物暴露水平更高,也展现出了和代谢领域其他靶点小分子更加适合联用的独特潜力。","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=nesSN20250824073313a6f7b306&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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全球最大的资产管理公司贝莱德最近晋升了其管理团队的一名高级成员,作为一系列更广泛的管理层变动的一部分,负责领导公司与美洲数千家企业的互动。贝莱德周五证实,董事总经理 Tanya Levy-Odom 目前在纽约领导贝莱德美洲投资管理团队。今年 7 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