NEW YORK and CAMBRIDGE, Mass., Nov. 04, 2025 (GLOBE NEWSWIRE) -- Royalty Pharma plc (Nasdaq: RPRX) today announced that it has acquired a royalty interest in Alnylam’s AMVUTTRA from funds managed by Blackstone Life Sciences (“Blackstone”) for $310 million. The royalty interest being sold stems from Blackstone’s 2020 financing collaboration with Alnylam, in which Blackstone invested to support AMVUTTRA’s pivotal Phase 3 HELIOS-B trial. AMVUTTRA is an FDA-approved RNAi therapeutic for the treatment of ATTR am ...

MONACO, Nov. 04, 2025 (GLOBE NEWSWIRE) -- Costamare Inc. (“Costamare” or the “Company”) (NYSE: CMRE) today reported unaudited financial results for the third quarter and nine-month period ended September 30, 2025. Discontinued operations as a result of Costamare Bulkers Holdings Limited Spin-Off The financial results for the nine-month period ended September 30, 2025, reflect the spin-off of Costamare’s dry bulk business (consisting of Costamare’s dry bulk owned fleet and its dry bulk operating platform, Co ...

Company expands partnership for employing a strategic focus on Bitcoin-native fintech, treasury services, and digital asset infrastructureLAS VEGAS, Nov. 04, 2025 (GLOBE NEWSWIRE) -- Bitcoin Bancorp. (OTC: BCBC) (“Bitcoin Bancorp” or the “Company”), a leading advisor in Bitcoin treasury strategies and institutional digital asset management, today announced a groundbreaking platform in partnership with Sailo Technologies to unveil a comprehensive Bitcoin treasury management system. This innovative crypto tre ...

Revenues increased 92% to $252 million YoYNet income increased to $123 million from ($125) million in Q3 2024Bitcoin holdings increased 98% YoY to 52,850 from 26,747 at the end of Q3 2024 Miami, FL, Nov. 04, 2025 (GLOBE NEWSWIRE) -- MARA Holdings, Inc. (NASDAQ: MARA) ("MARA" or the "Company"), a leading digital energy and infrastructure company, today announced its third quarter 2025 financial results in a letter to shareholders. Investors are invited to access the third quarter 2025 shareholder letter at M ...

CORAL GABLES, Fla., Nov. 04, 2025 (GLOBE NEWSWIRE) -- Relmada Therapeutics, Inc. (Nasdaq: RLMD, “Relmada” or the “Company”), a clinical-stage biotechnology company advancing innovative therapies for oncology and central nervous system indications, today announced the pricing of its underwritten offering of 40,142,000 shares of its common stock and, in lieu of common stock to certain investors, pre-funded warrants to purchase up to 5,315,000 shares of common stock. The shares of common stock are being sold a ...

Delivered $37.3 million total revenue in Q3 2025, representing 11% adjusted pro forma revenue growth versus Q3 2024 Generated Greenbrook clinic revenue of $21.8 million in Q3 2025, an increase of 25% on an adjusted pro forma basis versus Q3 2024 Continued cash management improvement, with cash used in operations of $0.8 million in Q3 2025 Strengthened balance sheet in Q3 2025, ending the quarter with $34.5 million of total cash, consisting of cash, cash equivalents, and restricted cash MALVERN, Pa., Nov. 04 ...

Q3 revenue increased 28% year-over-year to a record $181 million, driven by robust marketplace growth.Q3 marketplace revenue growth accelerated to 31% year-over-year, driven by strong enterprise growth and expanded networks of buyers and suppliers.Q3 gross profit increased 29% year-over-year to a record $72.0 million, driven by record marketplace gross margin of 35.7%.Q3 Adjusted EBITDA improved $6.8 million year-over-year to Adjusted EBITDA of $6.1 million driven by expanding marketplace gross margin and s ...

Prelude to prioritize development of mutant selective JAK2V617F JH2 inhibitor and KAT6A selective degrader programs Pausing further clinical development of SMARCA2 selective degrader programs JAK2V617F option agreement with Incyte, as previously announced, includes upfront payment of $35 million, a $25 million equity investment and $100 million if option is exercised Cumulative capital expected to fund planned operations into 2027 based on the Company’s preliminary estimates, and potentially into the third ...

MINNEAPOLIS, Nov. 04, 2025 (GLOBE NEWSWIRE) -- Celcuity Inc. (Nasdaq: CELC), a clinical-stage biotechnology company pursuing development of targeted therapies for oncology, today announced its participation in the Stifel 2025 Healthcare Conference to be held in New York on November 11-13, 2025. Brian Sullivan, Chief Executive Officer, and Co-founder of Celcuity, is scheduled for a fireside chat at 10:00 a.m. ET on Tuesday, November 11, 2025. A live webcast of the event will be available using this weblink h ...

核心观点 - 公司近期投资者日活动强调了其核心产品AXPAXLI™基于潜在优效标签、市场扩张和即时可应用性，有望重新定义视网膜疾病治疗标准[1] - 公司在湿性年龄相关性黄斑变性（wet AMD）的注册性临床项目中执行出色，SOL-1试验顶线数据预计在2026年第一季度读出，SOL-R试验顶线数据预计在2027年上半年读出[1] - 公司财务状况强劲，截至2025年9月30日现金余额为3.448亿美元，加上2025年10月股权融资获得的约4.45亿美元净收益，预计现金足以支撑运营至2028年[1][5] 临床项目进展 - **SOL-1试验（湿性AMD，优效性）**：试验按计划进行，顶线数据预计2026年第一季度读出，受试者保留率极高，超过95%的随机化受试者至今仍在研究中[3] - **SOL-R试验（湿性AMD，非劣效性）**：已完成555名受试者的目标随机化，顶线数据预计2027年上半年读出，试验设计包含24周筛选和导入期以降低患者变异性[3][4] - **HELIOS项目（NPDR）**：注册性项目即将启动，采用与FDA通过特殊方案评估（SPA）达成一致的新型有序糖尿病视网膜病变严重程度评分（DRSS）主要终点，旨在提高成功概率[1][7] - **SOL-X扩展研究**：一项为期36个月的开放标签扩展研究，旨在评估AXPAXLI的长期安全性和疗效，已完成SOL-1或SOL-R两年随访的受试者可入组进行额外三年随访[7] 市场机会与产品定位 - 抗VEGF药物的真实市场机会可能远超当前约150亿美元的年市场规模，市场扩张可能由数百万因当前治疗方案不可持续而停止治疗或治疗不足的湿性AMD患者驱动[2] - 非增殖性糖尿病视网膜病变（NPDR）的患病人数是湿性AMD的三倍，且目前无标准护理方案，为AXPAXLI提供了显著的扩张机会[2] - AXPAXLI有潜力成为首个在湿性AMD领域获得优于单剂量阿柏西普（2mg）优效性声明的产品标签[3] 财务状况 - **现金状况**：截至2025年9月30日，现金及现金等价物为3.448亿美元，加上2025年10月股权融资获得的约4.45亿美元净收益，公司预计现有资金可支持计划支出至2028年[5][7] - **第三季度业绩**：2025年第三季度净收入为1450万美元，较2024年同期的1540万美元下降5.8%，收入下降主要源于DEXTENZA在2025年面临更具挑战性的报销环境[6] - **运营支出**：2025年第三季度研发费用为5240万美元，高于2024年同期的3710万美元，增长主要源于持续进行的SOL-X扩展研究相关临床费用增加[7] 销售及营销费用为1310万美元，一般及行政费用为1600万美元[9][10] - **净亏损**：2025年第三季度净亏损为6940万美元，每股基本和摊薄净亏损均为0.38美元，2024年同期净亏损为3650万美元，每股亏损0.22美元[11] 产品与管线概述 - **AXPAXLI（OTX-TKI）**：一种研究性的、可生物降解的玻璃体内水凝胶，含有小分子多靶点酪氨酸激酶抑制剂阿西替尼，具有抗血管生成特性，目前正针对湿性AMD、糖尿病视网膜病变等视网膜疾病进行三期临床试验[14][34] - **DEXTENZA**：公司已上市产品，一种FDA批准的皮质类固醇，用于治疗成人和儿科患者眼科手术后的眼部炎症和疼痛，以及与过敏性结膜炎相关的眼部瘙痒[35] - **OTX-TIC**：研究中的曲伏前列素前房内水凝胶，已完成针对开角型青光眼或高眼压的二期临床试验，公司正在评估该项目的后续步骤[35]