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Inventiva to Host Analyst and Investor Event on October 8, 2025
Globenewswire· 2025-09-24 20:00
公司战略活动 - 公司将于2025年10月8日举办分析师与投资者活动,提供战略更新 [1] - 活动将在纽约市举行,并通过网络直播进行,时间为美国东部时间上午11:30至下午2:00 [1] - 活动议程包括公司管理层演讲以及代谢功能障碍相关脂肪性肝炎领域主要意见领袖和患者代表的见解 [2][5] 核心产品管线 - 公司主要资产为lanifibranor,一种用于治疗代谢功能障碍相关脂肪性肝炎的新型泛PPAR激动剂 [3] - 该药物正处于关键的NATiV3三期临床试验阶段,预计将在2026年下半年公布顶线结果 [5] - 活动将深入探讨lanifibranor的作用机制、二期临床试验的关键发现以及三期试验的设计与进展 [6] 行业专家参与 - 活动将邀请多位国际知名专家参与,包括哈佛医学院医学教授Nezam Afdhal博士 [6] - 伦敦玛丽女王大学肝病学教授兼研究主任William Alazawi博士也将出席 [6] - 三期NATiV3研究的共同主要研究者、弗吉尼亚联邦大学医学院的Arun Sanyal博士将参与讨论 [6] 市场定位与潜力 - 活动将讨论lanifibranor在巨大的全球代谢功能障碍相关脂肪性肝炎市场中的预期定位 [6] - 将重点介绍该药物因其独特的肝内和肝外双重活性,如何满足代谢功能障碍相关脂肪性肝炎治疗领域未满足的关键需求 [6] - 专家将阐述影响代谢功能障碍相关脂肪性肝炎治疗格局的关键趋势 [5]
Incyte Corporation (NASDAQ:INCY) Overview: Strategic Leadership and Market Performance
Financial Modeling Prep· 2025-09-24 18:00
公司概况 - 公司为专注于发现、开发和商业化专有治疗药物的生物制药企业 在肿瘤学及其他严重疾病领域拥有创新疗法[1] - 公司在行业中与大型制药公司竞争 通过战略领导和产品开发维持市场地位[1] 评级与股价表现 - RBC Capital于2025年9月24日将评级调整为"行业表现" 维持持有建议 同时将目标价从72美元上调至81美元[2] - 当前股价84.49美元 较前日下跌0.05美元(跌幅0.06%) 日内交易区间为84美元至84.72美元[4] - 过去52周股价波动区间为53.56美元至87.99美元 显示较大波动性[4] 管理层变动 - 公司任命Dave Gardner为执行副总裁兼首席战略官 该举措旨在加强领导团队建设[3] - 此次任命体现公司通过增强高管团队支持业务目标的战略承诺[3] 市场数据 - 公司市值约165亿美元 在生物制药行业具有重要市场地位[5] - 当日交易量为58,964股 显示中等投资者关注度[5]
Vor Biopharma upgraded to Buy at Stifel on telitacicept prospects
Seeking Alpha· 2025-09-24 16:04
股价表现 - 公司股价今日迄今上涨13% [3] 分析师评级与核心资产 - Stifel将公司评级从持有上调至买入 [3] - 评级上调源于对公司长期潜力信心增强 主要基于其核心资产telitacicept的前景 [3]
Rosen Law Firm Urges Cytokinetics, Inc. (NASDAQ: CYTK) Stockholders to Contact the Firm for Information About Their Rights
Businesswire· 2025-09-24 15:51
NEW YORK--(BUSINESS WIRE)--Rosen Law Firm, a global investor rights law firm, announces that a shareholder filed a class action on behalf of purchasers of common stock of Cytokinetics, Inc. (NASDAQ: CYTK) between December 27, 2023 and May 6, 2025. Cytokinetics describes itself as a "biopharmaceutical company focused on discovering, developing, and commercializing first-in-class muscle activators and next-in- class muscle inhibitors as potential treatments for debilitating diseases in which muscl. ...
Why Alnylam Pharmaceuticals (ALNY) is a Top Momentum Stock for the Long-Term
ZACKS· 2025-09-24 14:51
Zacks Premium服务 - 提供Zacks Rank和Zacks Industry Rank每日更新服务 [1] - 包含Zacks 1 Rank List、股票研究报告和高级选股筛选器 [1] - 提供Zacks Style Scores评分系统作为投资辅助工具 [1] Style Scores评分体系 - 采用字母评级系统(A/B/C/D/F)评估股票价值、成长和动量特性 [3] - 价值评分基于P/E、PEG、Price/Sales等比率识别折价股票 [3] - 成长评分综合预测和历史收益、销售额及现金流指标 [4] - 动量评分利用周价格变动和盈利预测月变化等因子 [5] - VGM评分整合所有风格评分形成综合指标 [6] 评分与排名协同应用 - Zacks Rank 1(强力买入)股票自1988年来年均回报达+23.64% [7] - 每日有超过200家Strong Buy和600家Buy评级公司 [8] - 建议优先选择Zacks Rank 1/2且Style Scores A/B的组合 [9] - 即使评分优异,4(Sell)或5(Strong Sell)评级股票仍存在下行风险 [10] Alnylam Pharmaceuticals案例 - 公司专注于RNA干扰技术治疗药物开发 [11] - 2018年Onpattro获美欧批准治疗hATTR淀粉样变性 - 2019年Givlaari获FDA批准治疗急性肝卟啉症 - 2020年Oxlumo获批治疗原发性高草酸尿症1型 - 2022年Amvuttra获FDA和EC批准并扩展适应症 - 当前Zacks Rank 3(Hold)评级且VGM评分B级 [12] - 动量评分A级,过去四周股价上涨0.7% [12] - 10位分析师60天内上调2025财年盈利预测2.06美元 [12] - 共识预期升至每股3.66美元,平均盈利惊喜达+348.4% [12]
Vivani Medical to Present at the Emerging Growth Conference on September 25, 2025
Globenewswire· 2025-09-24 13:15
ALAMEDA, Calif., Sept. 24, 2025 (GLOBE NEWSWIRE) -- Vivani Medical, Inc. (NASDAQ: VANI) (“Vivani” or the “Company”), a clinical-stage biopharmaceutical company developing miniature, ultra long-acting drug implants, today announced that it will present at the Emerging Growth Conference 86 on September 25, 2025. Vivani welcomes individual and institutional investors, along with advisors and analysts, to join its interactive presentation. This live online event will offer existing shareholders and the investme ...
New Data for BRIUMVI® Demonstrate 89.9% of Patients with Relapsing Multiple Sclerosis Were Free from Disability Progression After 6 Years of Continuous BRIUMVI Treatment
Globenewswire· 2025-09-24 13:10
During year 6 of continuous treatment with BRIUMVI the annualized relapse rate was 0.012, equivalent to one relapse occurring every 83 years of patient treatment Overall safety profile of BRIUMVI remained consistent over 6 years of continuous treatment, with no new safety signals emerging with prolonged treatment NEW YORK, Sept. 24, 2025 (GLOBE NEWSWIRE) -- TG Therapeutics, Inc. (NASDAQ: TGTX), today announced updated data presentations including new six-year data from the ULTIMATE I & II Phase 3 trials eva ...
Kyverna Therapeutics Highlights Potential of KYV-101 in Multiple Sclerosis with Data from Phase 1 Investigator-Initiated Trials to be Presented at ECTRIMS
Globenewswire· 2025-09-24 13:05
KYV-101 IIT data demonstrate promising clinical activity, including robust CAR T penetration into the central nervous system (CNS) and improved expanded disability status scale scores (EDSS) KYV-101 continues to demonstrate a tolerable safety profile, consistent with observations from the first 100 patients treated with KYV-1011 Encouraging early data of KYV-101 in multiple sclerosis highlights broader potential within neuroimmunology autoimmune diseases EMERYVILLE, Calif., Sept. 24, 2025 (GLOBE NEWSWIRE) - ...
Tiziana Life Sciences Announces Poster Presentation on Intranasal Foralumab Clinical Trial at the 41st ECTRIMS Congress
Globenewswire· 2025-09-24 12:30
BOSTON, Sept. 24, 2025 (GLOBE NEWSWIRE) -- Tiziana Life Sciences, Ltd. (Nasdaq: TLSA) (“Tiziana” or the “Company”), a biotechnology company developing breakthrough immunomodulation therapies with its lead development candidate, intranasal foralumab, a fully human, anti-CD3 monoclonal antibody, today announced that it will present a scientific poster at the 41st Congress of the European Committee for Treatment and Research of Multiple Sclerosis (ECTRIMS), being held September 24-26, 2025, in Barcelona, Spain ...
Cellectar and Evestia Clinical Announce Partnership to Support Auger-Emitting Radiopharmaceutical Clinical Trial in Triple-Negative Breast Cancer (TNBC)
Globenewswire· 2025-09-24 12:30
临床开发合作 - Cellectar Biosciences与合同研究组织Evestia Clinical达成协议,Evestia将为Cellectar的CLR 125治疗三阴性乳腺癌的1b期临床试验提供全面的CRO服务 [1] - 该合作将利用Evestia Clinical在肿瘤学领域的专业知识和全球能力,其经验涵盖超过300项涉及实体瘤和血液恶性肿瘤的研究 [2] - Cellectar计划于2025年第四季度在梅奥诊所启动针对三阴性乳腺癌的1b期临床试验 [1] 试验药物与方案 - CLR 125是一种靶向实体瘤的碘-125奥杰电子发射候选药物,其靶向适应症包括三阴性乳腺癌、肺癌和结直肠癌 [1] - Cellectar已选择梅奥诊所网络站点作为1b期临床试验的治疗中心,并任命Pooja Advani博士为首席研究员,确保患者由经验丰富的临床专家治疗 [3] 公司战略与背景 - Cellectar Biosciences是一家晚期临床生物制药公司,专注于利用其专有的磷脂药物偶联物平台开发靶向癌细胞的下一代治疗方法 [7] - 公司产品管线包括已获FDA突破性疗法认定的iopofosine I 131、基于锕-225的CLR 121225项目以及CLR 121125等项目 [8] - Evestia Clinical是一家全球专业CRO,通过近期与Atlantic Research Group合并,增强了其治疗专业知识和美国市场布局,能为肿瘤等复杂治疗领域提供定制化服务 [2][3] 疾病背景与市场机会 - 三阴性乳腺癌是一种侵袭性乳腺癌亚型,其特征在于缺乏雌激素受体、孕激素受体和HER2蛋白表达,使其治疗选择有限 [4] - 在美国,约12%的乳腺癌诊断属于三阴性乳腺癌,研究表明约25%(40,540例)的病例在标准治疗后会出现复发,存在对创新靶向疗法的迫切需求 [4]