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美股
详情
本页面由Tiger Fintech (Singapore) Pte. Ltd.提供服务
全球合伙
48.91
-1.8600
-3.66%
成交量:
3.66万
成交额:
179.68万
市值:
16.47亿
市盈率:
20.29
高:
50.98
开:
50.98
低:
48.14
收:
50.77
数据加载中...
总览
公司
新闻
公告
Global Partners盘中异动 急速下跌5.18%
市场透视
·
17小时前
GLP-1竞争新动向:礼来后来居上?
健识局
·
昨天
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
两大跨国巨头称霸GLP-1市场,国产减肥药的机会在哪?
澎湃新闻
·
04-19
减重GLP-1制剂将进入每日一次“口服”时代 礼来回应:已在准备产能计划
每日经济新闻
·
04-18
翰宇药业:全资子公司替尔泊肽原料药获韩国MFDS受理
美港电讯
·
04-18
【翰宇药业:全资子公司替尔泊肽原料药获韩国MFDS受理】翰宇药业公告,全资子公司翰宇药业(武汉)有限公司的替尔泊肽原料药获得韩国食品药品安全厅(MFDS)的审批受理。替尔泊肽是一种新型GLP-1/GIP双受体激动剂,适用于2型糖尿病、肥胖症等治疗。该药品的受理将完善公司产品版图,提升公司竞争力,有望对公司业绩增长和行业地位产生积极影响。
金融界
·
04-18
礼来预计年底前向全球监管机构提交orforglipron用于体重管理的上市申请
美港电讯
·
04-18
GLP-1减肥药市场博弈:礼来领航突破、辉瑞折戟沉沙,创新战如何取胜?
21世纪经济报道
·
04-18
礼来首个小分子口服GLP-1药物3期临床研究成功 有望颠覆减重药物格局
证券日报
·
04-18
美联邦法官裁定谷歌非法垄断部分广告技术市场;礼来首款GLP-1口服药报告积极三期试验结果丨全球科技早参
每日经济新闻
·
04-18
太平洋医药日报:礼来口服GLP-1受体激动剂ORFORGLIPRON三期临床成功
太平洋证券股份...
·
04-18
礼来(LLY.US)口服小分子GLP-1R激动剂III期研究成功
智通财经
·
04-17
【通化东宝利拉鲁肽注射液获哥伦比亚GMP证书】 近日,通化东宝与合作伙伴科兴生物制药股份有限公司携手的出海产品—利拉鲁肽注射液,正式获得哥伦比亚国家食品药品监督管理局颁发的GMP证书,为后续该产品在哥伦比亚的获批上市,以及拉美其他国家的市场准入打下坚实基础。利拉鲁肽注射液作为GLP-1受体激动剂,凭借其降糖、减重及心血管保护的多重疗效,已成为全球糖尿病治疗的一线药物,受到患者的广泛认可。
金融界
·
04-17
下一代减肥药:跨越GLP-1巅峰
医药魔方
·
04-16
辉瑞再终止GLP-1药物开发!罗氏、艾伯维等弯道超车?
医药经济报
·
04-15
1名受试者出现肝损伤,辉瑞终止一款口服减肥药临床开发,死磕小分子GLP-1
时代财经
·
04-15
辉瑞又双叒叕放弃一款口服 GLP-1,肥胖管线仅剩 1 款药物
Insight数据库
·
04-15
更多
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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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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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07:46","pubTimestamp":1745019966,"startTime":"0","endTime":"0","summary":"吃药减肥正在催生一个千亿级别的黄金赛道。高盛曾预估称,到2030年,全球抗肥胖症药物的市场规模可能会增长到约1000亿美元。在这条热门赛道,除了诺和诺德、礼来两大巨头你追我赶,另一边是包括更多中国药企也已跑步进场,展开竞速。国内已经有仁会生物的贝那鲁肽和华东医药的利拉鲁肽两款GLP-1药物正式获批减重适应证。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202504193381868266.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202504193381868266.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_eastmoney","symbols":["GLP","BK4590","BK4144"],"gpt_icon":0},{"id":"2528096721","title":"减重GLP-1制剂将进入每日一次“口服”时代 礼来回应:已在准备产能计划","url":"https://stock-news.laohu8.com/highlight/detail?id=2528096721","media":"每日经济新闻","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528096721?lang=zh_cn&edition=fundamental","pubTime":"2025-04-18 23:22","pubTimestamp":1744989770,"startTime":"0","endTime":"0","summary":"4月17日,礼来制药公布旗下口服GLP-1(胰高血糖素样肽-1)制剂“Orforglipron”的临床数据,在最高剂量下,每日服用一次Orforglipron的患者实现了平均减重7.3kg(7.9%)。这一表现超过了礼来之前预计的减重范围。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202504183381594279.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202504183381594279.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_eastmoney","symbols":["IE00BFTCPJ56.SGD","LU0096364046.USD","SG9999014898.SGD","LU1712237335.SGD","LU0943347566.SGD","LU2211815571.USD","LU1127390331.HKD","LU0708995401.HKD","LU2063271972.USD","LU1974910355.USD","LU2023250504.SGD","LU0238689110.USD","LLY","LU1623119135.USD","SG9999001176.USD","LU1061106388.HKD","LU0471298777.SGD","SG9999015945.SGD","LU2361044949.HKD","LU0385154629.USD","LU2265009873.SGD","LU0106261372.USD","SGXZ31699556.SGD","LU1720051017.SGD","BK4533","SGXZ51526630.SGD","LU0466842654.USD","LU1267930730.SGD","LU0882574139.USD","LU2324357040.USD","SG9999018857.SGD","LU0006306889.USD","SG9999014906.USD","LU1064131342.USD","BK4590","GLP","LU1868836914.USD","LU2089984988.USD","SGXZ81514606.USD","LU0079474960.USD","LU2491050071.SGD","LU1868836591.USD","LU2491050154.USD","SG9999014914.USD","LU1983299246.USD","LU2471134523.USD","LU1551013342.USD","LU2471134879.HKD","LU2602419157.SGD","LU0114720955.EUR"],"gpt_icon":1},{"id":"2528633910","title":"翰宇药业:全资子公司替尔泊肽原料药获韩国MFDS受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2528633910","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528633910?lang=zh_cn&edition=fundamental","pubTime":"2025-04-18 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15:37","pubTimestamp":1744961820,"startTime":"0","endTime":"0","summary":"全球GLP-1减肥药市场正迎来新一轮格局重塑。礼来在GLP-1赛道实现突破性进展之际,辉瑞却因安全性问题终止了口服GLP-1药物Danuglipron的研发,这也标志着其在该赛道的再次失利。在安全性方面,ACHIEVE-1研究中,orforglipron的整体安全性与GLP-1类药物一致。在礼来有效性、安全性均获得较好反响的同时,辉瑞安全性问题致口服赛道折戟。这是辉瑞在GLP-1减重药上的再次折戟。","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=nesSN2025041815395094d9c96c&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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有望颠覆减重药物格局","url":"https://stock-news.laohu8.com/highlight/detail?id=2528080431","media":"证券日报","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528080431?lang=zh_cn&edition=fundamental","pubTime":"2025-04-18 14:07","pubTimestamp":1744956431,"startTime":"0","endTime":"0","summary":"本报讯(记者李春莲见习记者梁傲男)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。4月17日,礼来股价收涨超14%,创下自2023年8月份以来的最大单日涨幅。","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://finance.eastmoney.com/a/202504183381169424.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_eastmoney","symbols":["LU0289739699.SGD","LU1988902786.USD","LU2211815571.USD","LLY","IE00B2B36J28.USD","LU0094547139.USD","LU1023059063.AUD","LU0006306889.USD","LU2357305700.SGD","SG9999014880.SGD","LU1366192091.USD","LU1057294990.SGD","LU1720051108.HKD","SG9999018865.SGD","IE00BK4W5L77.USD","SG9999013999.USD","BK4533","IE00BK4W5M84.HKD","LU2237443549.SGD","IE0004445239.USD","BK4581","LU2471134523.USD","IE0009355771.USD","SG9999015945.SGD","LU0882574055.USD","LU1232071149.USD","SG9999014898.SGD","IE00BJLML261.HKD","LU0820561818.USD","LU1127390331.HKD","LU0114720955.EUR","LU1064131342.USD","SG9999017495.SGD","SGXZ31699556.SGD","GLP","LU0417517546.SGD","LU0203202063.USD","LU2237443465.HKD","LU1814569148.SGD","LU1093756168.USD","LU0079474960.USD","LU2552382132.HKD","LU0385154629.USD","LU0471298694.HKD","LU0689472784.USD","LU1983299246.USD","LU2468319806.SGD","LU2237438978.USD","LU0061475181.USD","LU1280957306.USD"],"gpt_icon":1},{"id":"2528708741","title":"美联邦法官裁定谷歌非法垄断部分广告技术市场;礼来首款GLP-1口服药报告积极三期试验结果丨全球科技早参","url":"https://stock-news.laohu8.com/highlight/detail?id=2528708741","media":"每日经济新闻","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528708741?lang=zh_cn&edition=fundamental","pubTime":"2025-04-18 07:59","pubTimestamp":1744934384,"startTime":"0","endTime":"0","summary":"|2025年4月18日星期五|NO.1美联邦法官裁定谷歌非法垄断部分广告技术市场当地时间4月17日,美国一位联邦法官表示,谷歌公司非法垄断了两个在线广告技术市场。据悉,该裁决为检察官能够主张拆分谷歌公司的广告产品提供了可能性。当天晚些时候,谷歌在一份声明中表示,将对上述裁决提起上诉,称不同意法院关于其发布商工具的裁决。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202504183380604595.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202504183380604595.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["LU0234570918.USD","LU0444971666.USD","LU0957791311.USD","LU0690374961.EUR","LU0114720955.EUR","LU2097344357.USD","LU0648001328.SGD","GLP","LU0238689110.USD","LU0082616367.USD","LU0314106906.USD","LU1691799644.USD","LU0128525689.USD","LLY","LU0557290698.USD","LU1699723380.USD","IE00BJTD4N35.SGD","LU0006306889.USD","LU0203202063.USD","LU0251142724.SGD","LU0690374615.EUR","LU1267930490.SGD","BK4550","SGXZ31699556.SGD","LU0122379950.USD","LU2362541513.USD","LU2404859667.USD","IE00BYQQ9H92.USD","LU0225283273.USD","LU1435385759.SGD","LU1506573853.SGD","LU2360106947.USD","USJW.SI","GOOG","LU1066051498.USD","LU1814569148.SGD","GOOGL","SG9999014898.SGD","LU0308772762.SGD","LU1244550494.USD","LU0385154629.USD","IE00BK4W5L77.USD","LU0175139822.USD","SG9999014880.SGD","LU2362541273.HKD","LU0251132253.USD","LU2242650005.HKD","LU0788109477.HKD","GB00BDT5M118.USD","LU2471134952.CNY"],"gpt_icon":1},{"id":"2528080941","title":"太平洋医药日报:礼来口服GLP-1受体激动剂ORFORGLIPRON三期临床成功","url":"https://stock-news.laohu8.com/highlight/detail?id=2528080941","media":"太平洋证券股份...","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528080941?lang=zh_cn&edition=fundamental","pubTime":"2025-04-18 00:00","pubTimestamp":1744905600,"startTime":"0","endTime":"0","summary":"行业要闻:4 月17 日,礼来宣布,公司口服GLP-1受体激动剂Orforglipron 奥格列龙在一项关键的III 期临床试验中取得了具有统计学意义的积极结果。这项研究评估了Orforglipron 与安慰剂相比,在仅通过饮食和运动控制血糖不佳的成人2 型糖尿病患者中的安全性和有效性。Orforglipron 是一种研究性的、每日一次口服的小分子(非肽)胰高血糖素样肽-1 受体激动剂,可在一天中的任何时间服用,且不受食物和饮水限制。","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=nesSN2025041814031994d9b2b4&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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21:12","pubTimestamp":1744895544,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,4月17日,礼来宣布III期ACHIEVE-1研究取得积极结果,该研究评估了orforglipron与安慰剂相比在饮食和运动单独控制不佳的2型糖尿病成人中的安全性和疗效。Orforglipron是首个成功完成III期研究的口服小分子胰高血糖素样肽-1受体激动剂,服用时无需食物和水限制。礼来表示未来该药如果获批,将对其能够在全球范围内推出orforglipron且不受供应限制充满信心。","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/1280426.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":["LU0466842654.USD","LU2357305700.SGD","SG9999014898.SGD","LU0079474960.USD","LU1974910355.USD","LU1868836914.USD","IE00BK4W5L77.USD","LU0096364046.USD","SG9999014914.USD","LU2471134796.USD","LU0820561909.HKD","BK4007","LU2063271972.USD","LU2468319806.SGD","LU0203201768.USD","LU2552382058.USD","LU0256863902.USD","SGXZ99366536.SGD","IE00B2B36J28.USD","IE00BJLML261.HKD","LU1267930730.SGD","LU1868837300.USD","BK4581","SG9999015978.USD","SG9999015986.USD","SG9999015952.SGD","LU1548497426.USD","LU2112291526.USD","SG9999013999.USD","LU1989771016.USD","III","LU2361044865.SGD","LU1061106388.HKD","LU0320765059.SGD","SG9999014880.SGD","LU2324357040.USD","LU1814569148.SGD","LLY","LU2552382132.HKD","LU0097036916.USD","BK4533","SGXZ31699556.SGD","LU2471134523.USD","LU1064131342.USD","LU2750360997.AUD","GLP","LU2237443978.SGD","LU1917777945.USD","LU1868836757.USD","SG9999014906.USD"],"gpt_icon":1},{"id":"2528376858","title":"【通化东宝利拉鲁肽注射液获哥伦比亚GMP证书】 近日,通化东宝与合作伙伴科兴生物制药股份有限公司携手的出海产品—利拉鲁肽注射液,正式获得哥伦比亚国家食品药品监督管理局颁发的GMP证书,为后续该产品在哥伦比亚的获批上市,以及拉美其他国家的市场准入打下坚实基础。利拉鲁肽注射液作为GLP-1受体激动剂,凭借其降糖、减重及心血管保护的多重疗效,已成为全球糖尿病治疗的一线药物,受到患者的广泛认可。","url":"https://stock-news.laohu8.com/highlight/detail?id=2528376858","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528376858?lang=zh_cn&edition=fundamental","pubTime":"2025-04-17 15:41","pubTimestamp":1744875705,"startTime":"0","endTime":"0","summary":"近日,通化东宝与合作伙伴科兴生物制药股份有限公司携手的出海产品—利拉鲁肽注射液,正式获得哥伦比亚国家食品药品监督管理局颁发的GMP证书,为后续该产品在哥伦比亚的获批上市,以及拉美其他国家的市场准入打下坚实基础。利拉鲁肽注射液作为GLP-1受体激动剂,凭借其降糖、减重及心血管保护的多重疗效,已成为全球糖尿病治疗的一线药物,受到患者的广泛认可。","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/2025/04/17154149616448.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":["BK4139","BK0188","BK4144","600867","01477","BK1574","BK0196","SVA","BK0239","GLP","BK1191","BK4590"],"gpt_icon":0},{"id":"2527716404","title":"下一代减肥药:跨越GLP-1巅峰","url":"https://stock-news.laohu8.com/highlight/detail?id=2527716404","media":"医药魔方","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527716404?lang=zh_cn&edition=fundamental","pubTime":"2025-04-16 09:41","pubTimestamp":1744767666,"startTime":"0","endTime":"0","summary":"下一代减肥药的研发图谱,已然展开。相较于已诞生替尔泊肽这一明星药物的GLP-1/GIP组合,GLP-1与amylin的联用是更为新颖的尝试。罗氏明确表示,petrelintide具备单药治疗以及与GLP-1/GIP受体双重激动剂CT-388形成固定剂量组合的潜力。这并非礼来首次涉足三靶点减肥药研发。临床前数据显示,LX9851单药治疗可显著降低肥胖小鼠的体重、食物摄入量和脂肪量,与司美格鲁肽联合使用时,减重效果进一步增强,并有效减轻了GLP-1药物治疗后的体重反弹现象。","market":"us","thumbnail":"http://imgcloud.jrjimg.cn/2025/04/cms_20250416094106543.jpg","type":0,"news_type":0,"thumbnails":["http://imgcloud.jrjimg.cn/2025/04/cms_20250416094106543.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://ky.jrj.com.cn/2025/04/16094149570264.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":["GLP","BK4590","BK4144"],"gpt_icon":0},{"id":"2527490432","title":"辉瑞再终止GLP-1药物开发!罗氏、艾伯维等弯道超车?","url":"https://stock-news.laohu8.com/highlight/detail?id=2527490432","media":"医药经济报","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2527490432?lang=zh_cn&edition=fundamental","pubTime":"2025-04-15 19:34","pubTimestamp":1744716855,"startTime":"0","endTime":"0","summary":"4月14日,辉瑞宣布终止开发口服GLP-1激动剂Danuglipron,该药物此前正在研究用于慢性体重管理。这是辉瑞在GLP-1减重药上的再次折戟。在审查了全部信息后,包括迄今为止Danuglipron的所有临床数据以及监管机构的最新意见,辉瑞决定终止开发该分子。不可否认的是,摆在GLP-1赛道选手眼前的一大难关是肝损伤、胃肠道反应高等安全性问题。Petrelintide 耐受性良好,未发生严重或严重不良事件。","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=nesSN20250415194538a459a501&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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18:55","pubTimestamp":1744714542,"startTime":"0","endTime":"0","summary":"一款口服减重药折戟。图片来源:图虫创意跨国药企辉瑞又终止一款口服GLP-1R激动剂的临床开发。时代财经从辉瑞获悉,美国时间4月14日,辉瑞宣布决定终止开发每日一次的口服GLP-1R激动剂Danuglipron,该药物用于减重管理。由于安全性问题待解,辉瑞经多方考虑后选择终止开发这一小分子药物。而在Danuglipron之前,早在2023年6月,辉瑞就终止了其旗下另一款GLP-1R小分子激动剂项目Lotiglipron的后续研发。","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=nesSN20250415185615973879d2&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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