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Will Reblozyl Enable BMY to Offset the Impact of Generic Competition?
ZACKS· 2025-07-23 23:55
Key Takeaways BMY's Reblozyl posted Q1 sales of $478M, up 35% year over year, highlighting strong growth momentum. Reblozyl missed the primary endpoint in a phase III study for myelofibrosis-associated anemia treatment. BMY aims to consult FDA and EMA despite mixed phase III study results.Bristol Myers’ ((BMY) is striving hard for the label expansion of its key drugs. The company’s growth portfolio comprises Opdivo, Orencia, Yervoy, Reblozyl, Opdualag, Abecma, Zeposia, Breyanzi, Camzyos, Sotyku, Krazati a ...
Rising Cash Flows Make These 4 Stocks Worth Choosing Now
ZACKS· 2025-07-23 23:36
Key Takeaways CPRX, STKL, GAMB and ORN show rising cash flow trends versus their 5-year per-share averages. Each stock meets criteria, including price above $5, top broker ratings and a VGM Score of B or better. EPS estimates for 2025 have been revised upward recently, reflecting positive sentiment and momentum.We are already into the second-quarter reporting cycle, and stocks with top-line growth and increasing profit numbers might be popular choices. Moreover, choosing stocks based on a company’s effici ...
European Commission Approved DARZALEX Faspro® for Adult Patients with Smouldering Multiple Myeloma
Prnewswire· 2025-07-23 23:36
DARZALEX Faspro® is co-formulated with Halozyme's ENHANZE® drug delivery technologyApproval represents critical advancement in early intervention for multiple myelomaSAN DIEGO, July 23, 2025 /PRNewswire/ -- Halozyme Therapeutics, Inc. (NASDAQ: HALO) (Halozyme) today announced that Janssen-Cilag International NV, a Johnson & Johnson company, received European Commission (EC) approval of a new indication for DARZALEX Faspro® (daratumumab) co-formulated with ENHANZE®, as monotherapy for the treatment of adult ...
Why Array Technologies, Inc. (ARRY) is a Top Momentum Stock for the Long-Term
ZACKS· 2025-07-23 22:51
Zacks Premium服务概述 - Zacks Premium提供每日更新的Zacks Rank和Zacks Industry Rank、Zacks 1 Rank List的完全访问权限、股票研究报告和高级股票筛选工具,帮助投资者更明智、更自信地进行投资 [1] - 该服务还包括对Zacks Style Scores的访问权限 [1] Zacks Style Scores详解 - Zacks Style Scores是一套独特的指导方针,根据价值、增长和动量三种投资类型对股票进行评级,旨在作为Zacks Rank的补充指标,帮助投资者选择未来30天最有可能跑赢市场的证券 [2] - 每只股票根据其价值、增长和动量特征获得A、B、C、D或F的评级,评级越高,股票表现越好的可能性越大 [3] - Style Scores分为四个类别:价值评分、增长评分、动量评分和VGM评分 [3][4][5][6] 价值评分 - 价值评分考虑P/E、PEG、Price/Sales、Price/Cash Flow等多种比率,以突出最具吸引力和折扣的股票 [3] 增长评分 - 增长评分考察公司财务实力、健康状况和未来前景,包括预测和历史收益、销售额和现金流,以寻找可持续增长的股票 [4] 动量评分 - 动量评分利用一周价格变化和月度盈利预测百分比变化等因素,帮助确定买入高动量股票的有利时机 [5] VGM评分 - VGM评分结合价值、增长和动量三种评分,帮助投资者找到最具吸引力价值、最佳增长预测和最有望动量的公司 [6] Zacks Rank与Style Scores的结合 - Zacks Rank利用盈利预测修订的力量帮助投资者构建成功的投资组合,自1988年以来,1(强力买入)股票的平均年回报率为+23.62%,是同期标普500表现的两倍多 [7] - 每天可能有超过200家公司被评为1(强力买入),另有600家公司被评为2(买入),投资者可以从800多家顶级评级股票中选择 [8] - 投资者应选择Zacks Rank 1或2且Style Scores为A或B的股票,以最大化成功概率 [9] - 即使股票具有A或B的Style Scores,但如果其Zacks Rank为4(卖出)或5(强力卖出),其盈利前景仍呈下降趋势,股价下跌的可能性较大 [10] 关注股票:Array Technologies, Inc. (ARRY) - ARRY是一家专注于发现、开发和商业化靶向小分子药物的生物制药公司,用于治疗癌症和其他高负担疾病,其产品组合包括一种已上市的组合疗法Braftovi加Mektovi [11] - ARRY在Zacks Rank上被评为2(买入),VGM评分为A,动量评分为B,过去四周股价上涨10.8% [12] - 对于2025财年,三位分析师在过去60天内上调了盈利预测,Zacks共识估计增加了0.03美元至每股0.66美元,ARRY的平均盈利惊喜为+40% [12] - 凭借强劲的Zacks Rank和顶级的动量及VGM评分,ARRY应成为投资者的重点关注对象 [13]
Nkarta to Participate in the H.C. Wainwright “HCW@Home” Series
Globenewswire· 2025-07-23 20:01
文章核心观点 临床阶段生物制药公司Nkarta宣布参加H.C. Wainwright "HCW@Home"系列活动 [1] 活动信息 - 活动名称为H.C Wainwright "HCW@Home with Nkarta, Inc." [2] - 活动时间为2025年7月30日上午11:00(美国东部时间),形式为炉边谈话 [2] - 可在此处注册网络直播,活动将在Nkarta网站投资者板块同步直播,录像将在网站存档约90天 [2] 公司介绍 - Nkarta是临床阶段生物技术公司,致力于开发用于自身免疫性疾病的同种异体现成自然杀伤(NK)细胞疗法 [3] - 公司结合细胞扩增和冷冻保存平台、专有细胞工程技术和基于CRISPR的基因组工程能力,构建未来细胞疗法管线 [3] - 公司网址为www.nkartatx.com [3] 媒体/投资者联系方式 - 联系人是Nadir Mahmood,邮箱为nmahmood@nkartatx.com [4]
Novel Human Genetics Evidence Confirms Estimates of Genetic Prevalence, Underdiagnosis, and Potentially Greater Symptom Burden of Gain-of-Function CASR Variants Associated with ADH1
Globenewswire· 2025-07-23 19:30
- By examining over 100 unique variants associated with the CASR gene causative of ADH1, the average frequency of gain-of-function CASR variants was ~3.7 per 100,000, closely aligned to previously published estimates1 (3.9 per 100,000), which equates to approximately 25,000 carriers of ADH1-causing variants in the US and EU - Only ~20% of individuals with genetic variants linked to ADH1 were found to have an established diagnosis, highlighting a major gap in disease recognition and care - Nine novel gain-of ...
Clearside Biomedical Announces Approval of XIPERE® Suprachoroidal Treatment for Uveitic Macular Edema in Canada
Globenewswire· 2025-07-23 19:05
- XIPERE Now Approved for Use in Multiple Global Markets - - Continued Global Expansion and Validation of Clearside’s Suprachoroidal Space Injection Platform Featuring its Commercially Proven SCS Microinjector® - ALPHARETTA, Ga., July 23, 2025 (GLOBE NEWSWIRE) -- Clearside Biomedical, Inc. (Nasdaq: CLSD), a biopharmaceutical company revolutionizing the delivery of therapies to the back of the eye through the suprachoroidal space (SCS®), announced today that Health Canada has granted approval for XIPERE® (tr ...
Veeva OpenData and Veeva Network Enable Coordinated Customer Engagement for Boehringer Ingelheim
Prnewswire· 2025-07-23 19:03
PLEASANTON, Calif., July 23, 2025 /PRNewswire/ -- Veeva Systems (NYSE: VEEV) today announced Boehringer Ingelheim is the latest top 20 biopharma to standardize customer data across more than 100 countries with Veeva OpenData and Veeva Network. Accurate and comprehensive customer reference data from OpenData will equip Boehringer Ingelheim's teams with the insights needed to engage healthcare professionals (HCPs) with relevant information, while laying the data foundation to scale AI."Extending our trusted p ...
Scientist Dr. Akiko Iwasaki Joins SPEAR Study Group to Investigate Monoclonal Antibodies for Long COVID and COVID-19 Post-Vaccination Syndrome
Globenewswire· 2025-07-23 19:01
文章核心观点 公司宣布耶鲁大学医学院免疫生物学教授Akiko Iwasaki博士加入SPEAR研究小组 该小组聚焦与SARS-CoV-2病毒或COVID - 19疫苗刺突抗原持续存在相关的生物学和临床疾病或损伤 公司将利用单克隆抗体技术推动相关研究 探索针对长新冠和COVID - 19疫苗接种后综合征的治疗方案 [1][3] 公司动态 - 公司宣布Akiko Iwasaki博士加入SPEAR研究小组 [1] - SPEAR研究小组本月早些时候成立 旨在聚焦与SARS-CoV-2病毒或COVID - 19疫苗刺突抗原持续存在相关的生物学和临床疾病或损伤 [1] - SPEAR研究小组将构建并指导预期的临床试验 以严格评估单克隆抗体在长新冠和PVS患者中的安全性和探索性疗效 [3] - SPEAR研究小组正积极开展使用下一代抗体(如公司的研究性单克隆抗体候选药物VYD2311)对长新冠和PVS进行多中心转化临床研究 [4] 专家介绍 - Akiko Iwasaki博士在病毒发病机制、人类免疫生物学和病毒后慢性疾病(包括长新冠和COVID - 19疫苗接种后综合征)方面的开创性研究获得国际认可 [2] - 她是耶鲁大学COVID - 19康复研究的联合首席研究员 还领导了多项关于长新冠病理生物学的开创性研究 [2] 产品信息 PEMGARDA - PEMGARDA(pemivibart)是一种半衰期延长的研究性单克隆抗体 由adintrevimab工程改造而来 已证明对主要SARS-CoV-2变体具有体外中和活性 靶向SARS-CoV-2刺突蛋白受体结合域 [5] - PEMGARDA已获美国FDA紧急使用授权 用于某些中度至重度免疫功能低下的成人和青少年(12岁及以上 体重至少40公斤)的COVID - 19暴露前预防 [6] - PEMGARDA未获治疗COVID - 19、长新冠或暴露后预防COVID - 19的授权 暴露前预防不能替代推荐接种COVID - 19疫苗的人群接种疫苗 [7] - 支持PEMGARDA紧急使用授权采用了免疫桥接方法 但支持其益处的数据存在局限性 [9] VYD2311 - VYD2311是为COVID - 19开发的新型单克隆抗体候选药物 其药代动力学特征和抗病毒效力可能使其能够通过更方便患者的途径(如肌肉注射)提供具有临床意义的滴度水平 [11] - VYD2311使用公司专有的综合技术平台设计 利用了与pemivibart和adintrevimab相同的抗体骨架 [12] 公司概况 - 公司是一家生物制药公司 致力于提供针对严重病毒传染病(从SARS-CoV-2开始)的防护 采用行业独特的专有综合技术平台 [13] - 2024年3月 公司一款单克隆抗体获得美国FDA紧急使用授权 [13]
Neumora Therapeutics to Report Second Quarter 2025 Financial Results on Wednesday, August 6, 2025
Globenewswire· 2025-07-23 19:00
文章核心观点 Neumora Therapeutics公司将于2025年8月6日下午4点30分举办电话会议和网络直播公布2025年第二季度财务结果并进行业务更新 [1] 公司情况 - 公司是临床阶段生物制药公司,有七条脑部疾病治疗管线,其中三条处于临床阶段 [1][3] - 公司采取不同方法应对全球脑部疾病危机,工作由一系列工具支持以实现精准医疗 [3] - 公司使命是重新定义神经科学药物开发,为脑部疾病患者带来新一代疗法 [3] 会议信息 - 网络直播可在公司网站events and presentations板块观看,直播结束后有回放并存档30天 [2] - 参与者可在此处注册电话会议,建议提前至少10分钟注册 [2] 公司联系方式 - 联系人Helen Rubinstein,电话617 - 402 - 5700,邮箱Helen.Rubinstein@neumoratx.com [4]