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Global Partners Lp

54.00

+0.36000.67%

盘后：54.000.00000.00%16:04 EDT

成交量：7.11万

成交额：383.72万

市值：18.31亿

市盈率：17.26

高：54.60

开：53.28

低：52.46

收：53.64

数据加载中...

总览公司新闻公告

【众生药业：RAY1225注射液III期临床试验伦理批件获批】众生药业公告，控股子公司众生睿创自主研发的RAY1225注射液在超重/肥胖参与者的安全性和有效性的多中心、随机、双盲、安慰剂对照的III期临床试验(REBUILDING-2)获得组长单位北京大学人民医院和共同组长单位中山大学孙逸仙纪念医院伦理审查批件，批准项目开展。RAY1225注射液是众生睿创研发的、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，具有GLP-1受体和GIP受体双重激动活性，可通过刺激胰岛素分泌、延缓胃排空等机制调节人体代谢和控制血糖，有望用于降糖、减肥、代谢综合征等多种代谢性疾病的治疗。

野村升翰森制药目标价2%至18.36港元维持中性评级

通化东宝(600867.SH)：GLP-1/GIP双靶点受体激动剂获得降糖适应症Ib期临床试验总结报告

华东医药：GLP-1/GIP双靶点长效激动剂HDM1005注射液新适应症中国IND获得批准

华泰证券：全球GLP-1产品空缺较大，并购潮有望持续

华泰证券：全球GLP-1产品空缺较大，并购潮有望持续

GLP-1研发风云录：MetaBio折戟沉沙，辉瑞缘何错失良机？

【华东医药：HDM1005注射液临床试验申请获批】华东医药公告，2025年2月24日，全资子公司杭州中美华东制药有限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》，由中美华东申报的HDM1005注射液临床试验申请获得批准。HDM1005注射液用于阻塞性睡眠呼吸暂停（OSA）合并肥胖或超重成人患者的治疗，是多肽类人GLP-1受体和GIP受体的双靶点长效激动剂。该药物在中国的临床试验于2024年3月获得批准，适应症为2型糖尿病、超重或肥胖人群的体重管理。目前，HDM1005注射液正在积极推进II期临床试验相关工作。

华泰证券：国产GLP-1产品有望抢占全球市场份额

中信建投：出海迎来新机会，持续看好创新药行业

【中信建投：出海迎来新机会，持续看好创新药行业】中信建投研报表示，近年来，创新药企营业收入逐步增长，亏损实现缩窄，研发费用基本持平。在政策上，集采与医保谈判常态化，商保带来潜在增量，对创新药的支持力度有望进一步增加。在技术上，全球ADC药物2023年销售额达104亿美元，中国相关公司加速ADC布局与推进，逐渐迎来收获期；GLP-1减重赛道发展成熟，竞争从单一减重升级到多重获益，新靶点存在潜在出海机会；IO多抗赛道AK112率先实现突破，TCE技术从血液瘤走向实体瘤和自免。我国创新药全球竞争力持续增强，NewCo模式成为创新药出海新选择。国家政策鼓励创新药发展，新技术推动行业快速发展，出海迎来新机会，我们持续看好创新药行业。

金十数据整理：每日港股市场要闻速递（2月20日周四）

服用GLP-1降糖药后失明？诺和诺德回应：不能证实存在因果关系

每日经济新闻

歌礼制药-B(01672)宣布小分子口服GLP-1R激动剂ASC30美国Ib期多剂量递增研究前两个队列取得积极期中结果

Websea启动全球合伙人招募计划，携手共建加密生态新未来

Websea启动全球合伙人招募计划，携手共建加密生态新未来

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

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周四）","url":"https://stock-news.laohu8.com/highlight/detail?id=2512452187","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2512452187?lang=zh_cn&edition=fundamental","pubTime":"2025-02-20 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