Ad hoc announcement pursuant to Art. 53 LR Scemblix, a new first-line option for adults with CML, is first to show superior efficacy and favorable safety and tolerability profile in a Phase III trial vs. all standard of care (SoC) therapies1-3 Patients on Scemblix also had fewer dose reductions and half the rate of adverse reactions leading to treatment discontinuation1-3 Nearly 50% of CML patients do not meet efficacy milestones (MMR) with current SoC and almost 25% discontinue or switch the

2024年10月30日，临床超声AI领先企业北京视知觉智能科技有限公司（下称“视知觉”或“公司”）宣布完成新一轮数千万元融资，投资方为亦尚汇成投资基金（下称“亦尚汇成”）。本轮融资体现了医疗专业投资机构对AI赋能超声进入临床科室趋势的高度关注，以及对视知觉管理团队的高度认可。强云资本担任视知觉融资独家财务顾问并继续负责后续融资。 视知觉致力于为面向超声的诊断与治疗提供一站式人工智能解决方案，是临床超声AI领域的领航者。公司秉持医智融合理念，以中国研究型医院学会肌骨及浅表超声专委会医学专家为引领，以中国科学院自动化研究所智能技术专家为核心，在众多一流三甲医院的鼎力支持下，针对临床科室的实际需求，成功研发出肌骨超声实时动态人工智能辅助诊疗系统，实现了多组织实时动态分割，成功将疼痛、麻醉、康复、中医等临床治疗所需的活体解剖信息，转化为易懂、易用的结构化可视信息。 视知觉的肌骨超声实时动态人工智能辅助诊疗系统，为临床医生应用超声、超声医生走向临床提供了活体精细解剖（六大关节）可视化及辅助精准诊疗功能。这将大大缩短临床学习周期，提高医生工作效率。本系统使得疼痛（麻醉）可视化、康复可量化、外科

RMAT Designation Follows Positive Proof-of-Concept Data from the ALLO-316 TRAVERSE Trial in Adult Patients with Advanced or Metastatic CD70 Positive Renal Cell Carcinoma (RCC) Who Received Prior Immune Checkpoint Inhibitor and VEGF-Targeting Therapy ALLO-316 Advances Scientific Understanding and Applicability of the Dagger® Technology as the Next-Generation Allogeneic Platform to Maximize the Potential of a Single Infusion of an “Off-the-Shelf” CAR T Product Company to Present Updated Phase 1 Da

Findings offer potential mechanistic and clinical insights in the development of cellular therapy Lomecel-B™ for mild Alzheimer’s disease (AD) Lomecel-B™ capacity to inhibit MMP14 correlates with improved clinical and biomarker outcomes in mild AD Immunomodulatory and pro-vascular effects of Lomecel-B™ in mild AD potentially driven by ability to exert MMP14 inhibition which may protect TIE2 receptor integrity in human AD patients Oct. 29, 2024 -- Longeveron Inc. (NASDAQ: LGVN), a clinical stage

October 28, 2024 – BioPorto A/S (“BioPorto” or the “Company”) (CPH:BIOPOR), an in vitro diagnostics company focused on empowering the early detection of Acute Kidney Injury (AKI), today announced that it has entered into a global distribution partnership with Beckman Coulter, Inc., a global clinical diagnostics leader. Beckman Coulter will distribute BioPorto’s neutrophil gelatinase-associated lipocalin (NGAL) tests for use on Beckman Coulter family of DxC and AU clinical chemistry analyzers.

Oct. 28, 2024 -- Shuttle Pharmaceuticals Holdings, Inc. (Nasdaq: SHPH) (“Shuttle Pharma”), a discovery and development stage specialty pharmaceutical company focused on improving outcomes for cancer patients treated with radiation therapy (RT), announced today it has finalized agreements with all six of the planned site enrollment locations to administer the Phase 2 clinical trial of Ropidoxuridine for the treatment of patients with glioblastoma following the entry into agreements with Georgeto

Orally administered small molecule condensate modulators (c-mods) are a novel class of therapeutic agents designed to target condensates to modify disease DPTX3186 is Dewpoint’s first development candidate inhibiting beta catenin activity through a novel condensate mechanism for the treatment of Wnt-driven cancers DPTX3186 shows significant tumor growth inhibition, stasis, and regression in preclinical models of Wnt-driven cancers IND anticipated in mid-2025 followed by Phase 1 initiation in 2H

艾伯维（AbbVie）与Aliada Therapeutics宣布达成最终协议，艾伯维将以约14亿美元款项收购Aliada，并获得其主要项目阿尔茨海默病（AD）疗法ALIA-1758，目前该疗法正在1期试验当中受检视。此收购预计将在2024年第四季度完成。 Aliada是一家致力于利用新型血脑屏障（BBB）穿越技术开发治疗中枢神经系统（CNS）疾病创新疗法的生物技术公司。该公司专有的Modular Delivery（MODEL）平台专为高精度CNS药物递送而设计，其新型BBB穿越技术通过优化设计靶向转铁蛋白（TfR）和CD98受体的接合器，将各种生物载荷（如治疗性抗体和基因药物siRNA）递送至大脑。这些受体在脑部内皮细胞中高度表达。 ALIA-1758是一款采用该公司的创新递送技术，通过TfR将靶向焦谷氨酸化淀粉样蛋白（3pE-Aβ）抗体运输穿越BBB的在研AD疗法，该疗法旨在实现降解和清除淀粉样蛋白斑块，这是AD的病理特征。目前，该疗法正处于1期临床试验阶段，以评估其在健康受试者中的安全性和耐受性。 艾伯维执行副总裁、研发主管兼首席科学官Roopal Thakkar博士表示：

随着人口老龄化，以糖尿病性周围神经病理性疼痛（DPNP）、带状疱疹后神经痛（PHN） 为代表的周围神经病理性疼痛 （pNP）的发病率逐年增加。与此同时，过去20年对疼痛和痛觉的神经生物学研究也不断取得积极的进展，生物制药行业在探索不同机制pNP新药开发方面初见成效。 尽管已获批上市超过20年，加巴喷丁、普瑞巴林仍旧是周围神经病理性疼痛临床治疗的金标准。普瑞巴林作为第二代钙离子通道调节剂，与加巴喷丁相比，增强了与α2-δ 亚基的亲和力，滴定和起效更快，但仍旧不可避免嗜睡、头晕、周围性水肿、视物模糊等不良反应的发生。 第三代钙离子通道调节剂，通过提高对中枢神经系统α2δ亚基靶点亲和力，可进而提高疗效和降低不良反应发生率。2款第三代钙离子通道调节剂近年相续获得批准上市： 第一三共开发的Tarlige（Mirogabalin/美洛加巴林）2019年1月首次在日本获批上市用于神经性疼痛治疗。2024年6月在我国获批进口上市用于DPNP（商品名德力静）。 美洛加巴林对钙离子通道α2δ亚基具有较高的亲和力，且其与α2δ-1亚基解离缓慢，与α2δ-2亚基解离快速，该机制可能是其具有较好的镇痛治

– DURAVYU 2.7mg demonstrated an early and sustained improvement in BCVA with a gain of +8.9 letters compared to baseline - – DURAVYU 2.7mg demonstrated an early and sustained anatomical improvement mirroring BCVA results with a 68 micron reduction in CST - – Favorable safety profile continues with no DURAVYU-related ocular or systemic SAEs to date – – Full topline data anticipated in Q1 2025 – Oct. 28, 2024 -- EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT), a company committed to developing and