基于新加坡Hummingbird Bioscience独家授权的多有效载荷抗体-药物偶联技术和项目，Frazier Life Sciences推出Callio Therapeutics 融资由Frazier Life Sciences牵头，Jeito Capital以及包括Novo Holdings A/S、Omega Funds、ClavystBio、Platanus、Norwest、Pureos Bioventures、SEEDS Capital和EDBI在内的其他生命科学投资者大力参与 公司将推进创新的多有效载荷项目，通过克服现有单一有效载荷疗法的局限性，最大限度地提高癌症患者的治疗效果 2025年3月3日 -- 作为一家专注于通过多有效载荷抗体-药物偶联物（ADC）改善癌症治疗的生物技术公司，Callio Therapeutics今日宣布完成1.87亿美元A轮融资并正式启动。 此次融资由Frazier Life Sciences领投，Jeito Capital以及Novo Holdings A/S、Omega Funds、ClavystBio、Platanus、Norwest、

3月3日，丹擎医药 (“Danatlas Pharmaceuticals”）刚刚宣布完成新一轮1.5亿元人民币融资。本轮融资由康君资本领投，阿斯利康中金医疗产业基金、国方创新、磐霖资本等多家知名投资机构跟投，老股东红杉中国持续加注。根据新闻稿，本次融资将用于加速核心管线的临床研究、拓展创新技术平台及全球化战略布局。 丹擎医药自2021年成立以来，搭建了“合成致死”药物研发平台和转化医学平台。其核心产品PARG抑制剂（DAT-2645）已经获得中国NMPA和美国FDA批准开展临床1期研究，该产品正在中国开展临床1期的剂量递增研究，目前展示出良好的安全性、耐受性和抗肿瘤活性。同时，公司有多款创新候选药物研发管线推进至IND阶段。 据丹擎医药此前新闻稿介绍，DAT-2645的适应症包括乳腺癌、卵巢癌、胰腺癌、前列腺癌、子宫癌、胃癌、结直肠癌等多种常见癌症，并且有望拓展PARP抑制剂无效的适应症和解决PARP抑制剂耐药的痛点，具有潜在的“广谱治疗性”的临床应用前景。 除了DAT-2645，丹擎医药官网显示其管线中还包括了其他几款靶向“合成致死”靶点的新药，靶点包括了Polθ、WRN等等。

Specialist fund SCI Ventures, backed by major spinal cord injury foundations, together with existing investors, also participated in this round Proceeds will finance phase 1b/2a study of EG110A through safety and early efficacy results Opens way for clinical development across multiple medically important neuro-urology pathologies Funding will also support the company’s early-stage pipeline based on its proprietary HERMES vector technology platform. February 20, 2025 – EG 427, a biotechnology co

$3.7 Million Private Placement Financing from Existing Investors $2.0 Million Funding Advance from the Cancer Prevention and Research Institute of Texas (CPRIT) Feb. 18, 2025 Plus Therapeutics, Inc. (Nasdaq: PSTV) (the “Company,” or “Plus Therapeutics”), a clinical-stage pharmaceutical company developing targeted radiotherapeutics with advanced platform technologies for central nervous system (CNS) cancers, announced today that it has closed a private placement with aggregate initial upfront p

Bioxodes raises €2.7 million from existing investors in Series A extension Interim data from BIRCH intracerebral hemorrhage (ICH) Phase 2a trial in Q1 2025 Recruitment of up to 16 additional patients continues in BIRCH BIOX-101 Phase IIb ICH study preparations ongoing, to start upon close of Series B 12 February 2025 – Bioxodes SA, a clinical stage biopharmaceutical company developing novel therapies for the prevention and treatment of thrombotic and inflammatory diseases, has raised €2.7 millio

Feb. 10, 2025 -- ENA Respiratory, a clinical-stage pharmaceutical company developing antiviral host defence immune enhancers to minimize the impact of viral respiratory infections, announces today it has received a US$5 million investment from Flu Lab. Flu Lab, a California-based organization founded to advance innovative approaches for the prevention and treatment of influenza, provided the funding to support ENA’s clinical development of INNA-051. A simple to administer, virus-agnostic, sea

Feb. 03, 2025 Aplagon, a clinical stage biopharmaceutical company developing a first-in-class therapeutic for thrombo-inflammatory diseases, known as APAC, a heparin proteoglycan mimetic with antiplatelet and anticoagulant effects, announced today it has closed a EUR 7 million financing. The funding round was led by new investors Fåhraeus Startup and Growth AB (FSG), a Nordic venture capital fund, and European Innovation Council (EIC) Fund. FSG and EIC Fund were joined by leading Finnish inve

The Company has secured nearly $20 million in gross proceeds in 2025 ensuring complete funding for its pivotal CLARITY trial CLARITY is a prospective, randomized, multicenter study to validate Nociscan’s ability to improve surgical outcomes Nociscan aims to become the gold standard in identifying sources of low back pain through MR Spectroscopy (MRS) and Augmented Intelligence (AI) Feb. 04, 2025 -- Aclarion, Inc., (“Aclarion” or the “Company”) (Nasdaq: ACON, ACONW), a healthcare technology comp

Auron Therapeutics公司今日宣布，该公司完成2700万美元的B轮融资。同时，其潜在“first-in-class”的KAT2A/B蛋白降解剂AUTX-703的IND申请已经获得美国FDA的许可。该公司正在启动AUTX-703治疗血液恶性肿瘤的临床试验。 本次B轮融资由DCVC Bio领投，并得到了Apollo Health Ventures、Arkin Bio Ventures、BrightEdge、Casdin Capital、Franklin Berger、Mubadala Capital、Polaris Partners以及启明创投美国部的支持。 融资获得的资金将用于推进AUTX-703在急性髓系白血病（AML）患者中进行的1期临床概念验证试验，该试验将于今年第一季度开始患者招募。此外，部分资金还将用于评估靶向KAT2A/B在治疗自身免疫性疾病中的潜力，并推动利用该公司独有的AURIGIN药物发现平台针对上皮间质转化（EMT）肿瘤靶点的药物研发工作。 AUTX-703是一款潜在“first-in-class”口服KAT2A/B蛋白降解剂，由Auron通过其A

Dr Heather Preston, seasoned healthcare investor with over 30 years’ experience as a scientist, physician, management consultant, and Board adviser, joins as Chair Funding recognises Harness’ significant progress in unexplored targets for CNS disease and accelerates selection of clinical candidate for lead programme (FAN1) in Huntington’s Disease Harness’ unique approach builds on recent research published in Nature Medicine and Cell 27 January 2025: Harness Therapeutics (‘Harness’), a biotechno