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美股
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Global Partners Lp
53.64
+0.4900
0.92%
成交量:
3.81万
成交额:
203.34万
市值:
18.19亿
市盈率:
17.15
高:
54.34
开:
53.42
低:
52.46
收:
53.15
数据加载中...
总览
公司
新闻
公告
GLP-1市场激战!“减肥药双雄”下调2025年预期
国际金融报
·
05-08
礼来盘前涨超1% 口服GLP-1降压药在华获批临床
金吾资讯
·
05-07
司美格鲁肽全球销售额超过抗癌药物K药 暂时坐上了全球“药王”宝座
美港电讯
·
05-07
首次将减肥药纳入基本药物目录?世卫组织回应:相关方案正在制定 预计最早8月份出台
美港电讯
·
05-07
速递|礼来全球首个口服GLP-1降压药,在华获批临床!
GLP1减重宝典
·
05-07
翰宇药业:利拉鲁肽原料药获韩国MFDS受理
美港电讯
·
05-06
礼来2025Q1:营收增长45%,GLP-1美国市场处方量超过诺和诺德
动脉网
·
05-02
礼来一季度净利增近三成,明星GLP-1药物替尔泊肽贡献近半收入
澎湃新闻
·
05-01
RWA永续产品危机:为什么GLP模式注定撑不住RWA永续?
Blockbeats
·
04-30
【益诺思:子公司通过美国FDA检查】益诺思公告,公司全资子公司益诺思南通于2024年10月28日至2024年11月1日期间接受了来自美国食品药品监督管理局(FDA)的良好实验室规范(GLP)全面现场检查。近日,公司收到FDA签发的现场检查报告(EIR,Establishment Inspection Report),该报告表明公司通过了本次美国FDA的GLP检查。益诺思南通首次通过美国FDA GLP现场检查,GLP体系建设得到进一步完善。公司及全资子公司益诺思南通已均具备了开展符合NMPA、美国FDA以及OECD GLP要求的药物非临床安全性评价研究的能力,公司的国际化服务水平得到了全面提升,可为全球的医药企业和科研机构提供全方位的符合国内及国际申报标准的新药研究服务。本次全资子公司益诺思南通通过美国FDA GLP现场检查对公司的当期经营业绩不构成重大影响。
金融界
·
04-29
口服GLP-1“上桌”,电商成新战场?
CHC医疗传媒
·
04-29
加入GLP-1混战,“中国本土丙肝药一哥”换赛道,歌礼制药欲靠减肥药翻身
时代财经
·
04-28
机构报告:我国去年投资交易总额达470亿美元
美港电讯
·
04-27
迎战礼来,诺和诺德抢先递交口服 GLP-1减重上市申请
动脉网
·
04-23
歌礼制药-B(01672):小分子口服GLP-1R激动剂ASC30美国Ib期多剂量递增研究取得积极顶线结果及已向FDA递交IIa期研究方案(13周疗程)
智通财经
·
04-23
Global Partners盘中异动 急速下跌5.18%
市场透视
·
04-22
GLP-1竞争新动向:礼来后来居上?
健识局
·
04-21
医药行业周报:礼来首个小分子口服GLP-1药物3期临床研究成功 有望改变减重药物格局
平安证券股份有...
·
04-20
医药行业周报:本周医药下跌0.4% 人民时评要求保证药企药店利润空间 礼来口服GLP-1治疗糖尿病研发成功
上海申银万国证...
·
04-20
诺和诺德、礼来“二王争霸”,国产GLP-1抢夺新适应症,恒瑞医药们不想只做减肥神药
时代财经
·
04-19
更多
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18:39","pubTimestamp":1746700740,"startTime":"0","endTime":"0","summary":"近日,“减肥药双雄”礼来和诺和诺德先后发布2025年一季报。不过,值得注意的是,尽管GLP-1产品销量一路高歌猛进,但两家药企对于2025年公司的整体预期仍持保守态度。GLP-1产品销量大增当地时间5月7日,诺和诺德发布公司2025年第一季度业绩报告。口服剂型预备上市GLP-1药物市场上“减肥药双雄”激战正酣,目前来看双方都把重心寄予在了口服剂型上。礼来的口服小分子GLP-1药物Orforglipron目前也已进入临床末期。","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=nesSN20250508185103a6d790e4&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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11:41","pubTimestamp":1746589262,"startTime":"0","endTime":"0","summary":"目前,礼来正围绕Orforglipron推进多项三期研究,涵盖2型糖尿病治疗、体重相关合并症的体重控制,以及阻塞性睡眠呼吸暂停与高血压等适应症。根据ClinicalTrials.gov网站信息,礼来于2025年5月1日注册了一项三期试验,评估该药在超重或肥胖且患有高血压的成年患者中的疗效。此外,今年4月21日,礼来公布了Orforglipron在2型糖尿病治疗中的三期临床数据,显示该药在安全性和耐受性方面与注射类GLP-1药物相当。","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=nesSN20250507151017a6d5f8df&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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21:28","pubTimestamp":1746019680,"startTime":"0","endTime":"0","summary":"对于用加密衍生品做多或做空 RWA 的需求已经非常明显了。而且不同于 HLP 模式可以在链上部分对冲敞口,OLP 模式下没有稳定机制去对冲 RWA 的风险暴露。在我个人看来,作为一个热爱 RWA 永续概念的人,这才是 RWA 永续产品唯一可持续的长期模式,不仅是对 Ostium,对 Gains,以及所有相关项目都是如此。GLP/\"赌场式\"模式只能用于冷启动阶段,长期发展是不现实的,这已经被多次验证了。","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":"https://www.theblockbeats.info/news/58016","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":"theblockbeats_zh_highlight","symbols":["BK4590","BK4144","GLP"],"gpt_icon":0},{"id":"2531375872","title":"【益诺思:子公司通过美国FDA检查】益诺思公告,公司全资子公司益诺思南通于2024年10月28日至2024年11月1日期间接受了来自美国食品药品监督管理局(FDA)的良好实验室规范(GLP)全面现场检查。近日,公司收到FDA签发的现场检查报告(EIR,Establishment Inspection Report),该报告表明公司通过了本次美国FDA的GLP检查。益诺思南通首次通过美国FDA GLP现场检查,GLP体系建设得到进一步完善。公司及全资子公司益诺思南通已均具备了开展符合NMPA、美国FDA以及OECD GLP要求的药物非临床安全性评价研究的能力,公司的国际化服务水平得到了全面提升,可为全球的医药企业和科研机构提供全方位的符合国内及国际申报标准的新药研究服务。本次全资子公司益诺思南通通过美国FDA GLP现场检查对公司的当期经营业绩不构成重大影响。","url":"https://stock-news.laohu8.com/highlight/detail?id=2531375872","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2531375872?lang=zh_cn&edition=fundamental","pubTime":"2025-04-29 21:50","pubTimestamp":1745934648,"startTime":"0","endTime":"0","summary":"近日,公司收到FDA签发的现场检查报告,该报告表明公司通过了本次美国FDA的GLP检查。公司及全资子公司益诺思南通已均具备了开展符合NMPA、美国FDA以及OECD GLP要求的药物非临床安全性评价研究的能力,公司的国际化服务水平得到了全面提升,可为全球的医药企业和科研机构提供全方位的符合国内及国际申报标准的新药研究服务。本次全资子公司益诺思南通通过美国FDA GLP现场检查对公司的当期经营业绩不构成重大影响。","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":"https://24h.jrj.com.cn/2025/04/29215050019076.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":"jinrongjie_stock","symbols":["BK0216","BK4590","688710","BK4144","GLP"],"gpt_icon":0},{"id":"2531224178","title":"口服GLP-1“上桌”,电商成新战场?","url":"https://stock-news.laohu8.com/highlight/detail?id=2531224178","media":"CHC医疗传媒","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2531224178?lang=zh_cn&edition=fundamental","pubTime":"2025-04-29 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07:23","pubTimestamp":1745364228,"startTime":"0","endTime":"0","summary":"智通财经APP讯,歌礼制药-B 发布公告,公司董事会宣布其ASC30每日一次口服片在美国肥胖症受试者中开展的随机、双盲、安慰剂对照Ib期多剂量递增 研究取得积极顶线结果。该Ib期MAD研究包含3个队列,每一个队列采用不同的周剂量递增方案,治疗期4周及随访1周。ASC30片Ib期研究的耐受性与疗效数据均支持ASC30每日一次口服片IIa期研究设计采用“更低起始剂量与更缓递增速度”的策略。公司预计美国IIa期研究将于2025年第三季度初开展。","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/1282831.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":["BK4144","BK1574","01672","BK1191","GLP","BK1161","01477","BK1515","BK4590"],"gpt_icon":0},{"id":"2529339385","title":"Global Partners盘中异动 急速下跌5.18%","url":"https://stock-news.laohu8.com/highlight/detail?id=2529339385","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529339385?lang=zh_cn&edition=fundamental","pubTime":"2025-04-22 01:55","pubTimestamp":1745258158,"startTime":"0","endTime":"0","summary":"北京时间2025年04月22日01时55分,Global Partners股票出现异动,股价急速下挫5.18%。Global Partners股票所在的油气中游产业行业中,整体跌幅为4.24%。其相关个股中,Imperial Petroleum Inc (Marshall Is 8.75% Cum Red Perp Pfd A、BPT信托、Imperial Petroleum Inc.涨幅较大,Scorpio Tankers Inc.、Viper Energy, Inc.、Kinetik Holdings Inc.较为活跃,换手率分别为0.57%、0.50%、0.49%,振幅较大的相关个股有Cbl International Limited、Robin Energy Ltd.、Dynagas Lng Partners Lp,振幅分别为15.79%、14.03%、9.44%。Global Partners公司简介:Global Partners LP是一家作为中游物流和营销公司的有限合伙企业。","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=nesSN20250422015558973fa34a&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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11:05","pubTimestamp":1745204734,"startTime":"0","endTime":"0","summary":"尽管GLP-1火遍全球,但实际上,现在还没有任何一款GLP-1口服版药物获批了减重适应症。GLP-1尽管看来已经接近完美,但依然有很大的不足。口服药就完全规避了以上所有劣势,从诺和诺德、礼来的开发劲头可以看出,今后GLP-1药物的竞争会逐渐从注射剂转到口服制剂上。口服减肥GLP-1可能会成为礼来反超的一张王牌。","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=nesSN20250421110753a4606b12&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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有望改变减重药物格局","url":"https://stock-news.laohu8.com/highlight/detail?id=2528386165","media":"平安证券股份有...","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528386165?lang=zh_cn&edition=fundamental","pubTime":"2025-04-20 00:00","pubTimestamp":1745078400,"startTime":"0","endTime":"0","summary":"行业观点礼来首个小分子口服GLP-1药物3期临床研究成功,有望改变减重药物格局4月17日,全球制药巨头礼来公司公布了3期临床研究ACHIEVE-1的积极顶线结果,该研究评估了Orforglipron与安慰剂相比,在患有2型糖尿病和仅通过饮食和运动控制不足的成人中的安全性和有效性。鉴于患者在研究结束时尚未达到体重平台期,可能表明尚未实现完全减重。公司目前也在研究Orforglipron对非糖尿病患者的减重效果。若获批,Orforglipron将成为第二款在美国上市的GLP-1口服药。","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=nesSN20250420221112973e6626&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, 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人民时评要求保证药企药店利润空间 礼来口服GLP-1治疗糖尿病研发成功","url":"https://stock-news.laohu8.com/highlight/detail?id=2528003866","media":"上海申银万国证...","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528003866?lang=zh_cn&edition=fundamental","pubTime":"2025-04-20 00:00","pubTimestamp":1745078400,"startTime":"0","endTime":"0","summary":"礼来口服GLP-1 治疗糖尿病研发成功:4 月17 日,礼来宣布首个小分子口服GLP-1RA药物Orforglipron 3 期临床研究成功,ACHIEVE-1 取得了积极的顶线结果。Orforglipron 成为了首个成功完成3 期试验、对饮食或饮水不加以限制的口服小分子GLP-1 受体激动剂。礼来预计将在今年年底前向全球监管机构提交Orforglipron 用于体重管理的上市申请,预计于2026 年提交其用于治疗2 型糖尿病的上市申请。要求国会山调整IRA 药品谈判,旨在进一步降低处方药价格。","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=nesSN2025042021145194dbdd41&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description 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