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诺华肾病治疗创新药诺锐达®(盐酸阿曲生坦片)在京东健康全网首发
证券日报之声· 2025-12-12 18:14
未来,京东健康将继续依托其坚实的医药健康服务生态,在肾病等慢性疾病管理领域深耕。通过与诺华 这样的全球领先药企深化合作,京东健康不仅将持续引入如诺锐达®这样的前沿治疗药物,更将聚焦于 为患者提供覆盖全病程的数字化健康管理解决方案,有效提升我国肾病患者乃至更广泛慢病人群的生命 质量。 (编辑 张明富) 本报讯 (记者袁传玺)12月12日,诺华公司旗下创新药物诺锐达®(盐酸阿曲生坦片)在京东健康线 上首发。该药物是中国首个获批、用于降低有疾病快速进展风险的原发性免疫球蛋白A肾病(IgA肾 病)成人患者蛋白尿的非免疫性疗法,也是国内目前唯一针对此适应症的高选择性内皮素A(ETA)受 体拮抗剂。京东健康将依托"新特药全网首发第一站"的能力优势,凭借其强大的供应链履约能力、专业 药师服务,助力创新药物更快速、更精准、更可及地触达全国患者。 据了解,IgA肾病作为一种常见的原发性肾小球疾病,在我国青壮年人群中高发,尤其集中于20至30岁 年龄阶段。疾病初期症状隐匿,但病情持续进展风险高。临床研究显示,若未能有效控制,约半数伴有 持续性蛋白尿的IgA肾病患者可能在确诊后的10至20年内发展至肾衰竭,最终不得不依赖终身透析或 ...
Novartis AG (NVS) Gets Upgraded to Overweight from Neutral by JPMorgan
Yahoo Finance· 2025-12-11 00:28
公司评级与目标价调整 - 摩根大通将诺华公司评级从“中性”上调至“增持” [1] - 摩根大通将诺华公司目标价从95瑞士法郎大幅上调至125瑞士法郎 [1] - 此次评级调整是摩根大通对欧洲制药板块2026年展望的一部分 [1] 核心产品进展与市场地位 - 诺华公司的基因疗法Itvisma于11月24日获得美国FDA批准 [3] - Itvisma获批用于治疗2岁及以上儿童、青少年和成人脊髓性肌萎缩症患者 [3] - 该疗法是首个也是唯一一个适用于该广泛人群的基因替代疗法 [3] - 在三期研究中,无论患者SMA治疗史如何,Itvisma均显示出运动功能改善和病情稳定 [4] - 该疗法为一次性给药,可替代SMN1基因,可能减少对慢性SMA治疗的需求 [4] - 目前该基因替代疗法已适用于所有符合条件的SMA患者,不受年龄限制 [4] 行业与公司背景 - 摩根大通预计制药板块表现将由研发管线进展驱动 [2] - 摩根大通下调了那些在2026年缺乏研发管线进展的公司的评级 [2] - 诺华公司总部位于瑞士巴塞尔,业务涵盖开发、营销和制造医疗保健及医药产品 [5] - 公司运营分为创新药物、山德士和公司总部三大板块 [5]
Novartis' Investigational Drug Reports Longer Disease Control In Patients With Rare Blood Disorder
Benzinga· 2025-12-10 03:32
Novartis AG (NYSE:NVS) on Tuesday shared results from the VAYHIT2 Phase 3 trial of ianalumab plus eltrombopag in patients with primary immune thrombocytopenia (ITP) previously treated with corticosteroids.In August, Novartis shared topline results from the VAYHIT2 trial.Ianalumab (9 mg/kg) plus eltrombopag extended ITP disease control by 45%, based on the primary endpoint of time to treatment failure (TTF), which assesses how long patients maintain safe platelet levels during and after the treatment period. ...
Novartis AG (NVS) Announces US FDA Approval of Itvisma®
Yahoo Finance· 2025-12-10 00:19
Novartis AG (NYSE:NVS) is one of the Most Undervalued Stocks to Buy Right Now. On November 24, the company announced that the US FDA approved Itvisma® (onasemnogene abeparvovec-brve) for treating children of 2 years and older, teens, and adults having spinal muscular atrophy (SMA) with a confirmed mutation in the survival motor neuron 1 (SMN1) gene. Novartis AG (NYSE:NVS) highlighted that Itvisma has been uniquely designed to address the genetic root cause of SMA with a one-time fixed dose that doesn’t req ...
Tiny Biotech Terns Takes Aim At Novartis' Leukemia Blockbuster
Benzinga· 2025-12-09 20:51
Terns Pharmaceuticals, Inc. (NASDAQ:TERN) on Monday presented updated and expanded data from the ongoing CARDINAL trial of TERN-701 in previously treated chronic myeloid leukemia (CML) patients at the American Society of Hematology Annual Meeting and Exposition.As of the cutoff date of September 13, 2025, 63 patients were enrolled.DataOf 38 efficacy-evaluable patients, the overall (cumulative) major molecular response (MMR) rate was 74% (28/38) by 24 weeks, with 64% (18/28) achieving MMR and 100% (10/10) ma ...
Novartis ianalumab significantly extends disease control in patients with immune thrombocytopenia with only four once-monthly doses
Globenewswire· 2025-12-09 20:30
Ianalumab (9 mg/kg) plus eltrombopag extended ITP disease control by 45% with patients maintaining disease control 2.8 times longer than with placebo plus eltrombopag1,2 62% of patients treated with ianalumab plus eltrombopag achieved sustained platelet response at six months compared to 39% with placebo plus eltrombopag1,2Ianalumab, administered as four once-monthly intravenous doses in the ITP setting, has the potential to reduce the need for chronic treatment and deliver durable disease control in ITPNov ...
1 in 4 metastatic breast cancer patients treated with Novartis Kisqali® remain progression-free beyond 4 years
Globenewswire· 2025-12-09 20:15
Progression-free response stayed consistent across age, BMI, and menopausal status in MONALEESA pooled analysis1 KISQALI is only CDK4/6i to demonstrate statistically significant overall survival (OS) in MBC across all Phase III trials2-12New NATALEE 5-year sub-analysis data reinforce sustained reduction in distant disease-free survival in broadest population of EBC patients13 Basel, December 9, 2025 – Novartis today announced results showing that one in four patients with hormone receptor-positive, human e ...
【美股盘前】美国将允许对华出售H200芯片,英伟达涨1.6%;拟发20亿美元可转债,CoreWeave跌1.3%;AI借贷狂潮愈演愈烈,穆迪警告:整个金...
每日经济新闻· 2025-12-09 18:24
美股股指期货表现 - 截至发稿,道指期货涨0.05%、标普500指数期货涨0.13%、纳指期货涨0.14% [1] 中概股市场动态 - 中概股盘前普跌,阿里巴巴跌1.92%,拼多多跌1.38%,百度跌3.88%,京东跌1.3%,小鹏汽车跌2.58% [1] 美国对华AI芯片销售政策 - 美国总统特朗普表示,美国将允许英伟达向中国“经批准的客户”出售H200人工智能芯片,芯片销售收入的25%将上缴美国政府 [1] - 此举同样适用于超威半导体公司(AMD)、英特尔和其他美国公司 [1] - 截至发稿,英伟达股价涨1.6%,AMD涨1.3%,英特尔涨0.7% [1] 伊拉克油田股权潜在变动 - 遭美国制裁的俄罗斯卢克石油公司在伊拉克一座油田项目中的股权可能由美国石油巨头接手 [2] - 伊拉克方面属意埃克森美孚,雪佛龙公司也是潜在接盘方 [2] 汽车行业合作与产品开发 - 跨国汽车制造商Stellantis与欧洲移动出行平台Bolt宣布合作,共同探索在欧洲开发和部署用于商业运营的L4级无人驾驶汽车 [2] - 双方计划从2026年开始部署测试车辆,初步目标是在2029年实现量产 [2] - 截至发稿,Stellantis股价跌近1% [2] - 雷诺将与福特汽车携手,针对欧洲市场合作开发平价小型电动车,并联合生产商用货车 [3] - 计划推出的两款小型电动车中,首款将在法国北部的雷诺工厂生产,预计将在2028年展示 [3] 生物科技与制药合作 - 英国生物科技公司Relation Therapeutics与诺华达成合作,旨在发现并推进特应性疾病的新靶点 [3] - Relation将获得5500万美元初始款项,并有资格获得至多17亿美元的里程碑付款及产品净销售额的分级特许权使用费 [3] - 截至发稿,诺华股价涨1.8% [3] 公司融资与债务动态 - CoreWeave计划通过私募方式发行2031年到期的可转换优先票据,规模为20亿美元 [4] - 截至9月底,CoreWeave的债务总额已达140亿美元 [4] - 截至发稿,CoreWeave股价跌1.3% [4] - 美国医疗用品巨头Medline计划通过发行1.79亿股股票筹集至多53.7亿美元,公司估值最高可达553亿美元 [4] AI行业债务风险警示 - 穆迪首席经济学家马克•赞迪表示,2025年人工智能超大规模企业通过创纪录的债券发行累积了高额债务,债务规模超过互联网泡沫破裂前夕科技企业的借贷水平 [4] - 警告称,人工智能公司的借贷问题可能成为整个金融体系和经济增长的潜在威胁 [4]
美股异动丨诺华制药盘前涨近2%,布局过敏性疾病新靶点
格隆汇· 2025-12-09 17:30
诺华制药(NVS.US)盘前涨近2%,报132.73美元。消息面上,诺华制药与英国生物技术公司 Relation Therapeutics达成一项高达逾17亿美元的交易,以帮助寻找治疗过敏性疾病的药物靶点。该交易旨在将 诺华制药在免疫皮肤病学方面的专业知识与Relation的药物发现人工智能平台相结合,后者借助包括人 体组织在内的患者数据来揭示疾病表现的遗传基础。(格隆汇) ...
Relation announces strategic collaboration with Novartis to advance therapeutics for atopic diseases
Globenewswire· 2025-12-09 16:00
LONDON, Dec. 09, 2025 (GLOBE NEWSWIRE) -- Relation today announced a multi-program, strategic collaboration with Novartis to discover and advance novel targets for atopic diseases. Under the terms of the agreement, Relation will receive $55 million, comprising an upfront payment, equity investment and additional R&D funding. In addition, Relation is eligible to receive preclinical, development, regulatory, and commercial sales milestones of up to $1.7 billion, along with tiered royalties on net sales of pro ...