当前位置:首页 > 报告详情

EYPT JPM2026 Presentation_vF.pdf

上传人: 明**** 编号:1069754 2026-01-17 27页 2.53MB

1、 2026 EyePoint.All Rights Reserved.J.P.Morgan Healthcare Conference PresentationJanuary 13,2026Jay S.Duker,M.D.President and CEO 2026 EyePoint.All Rights Reserved.2Legal DisclaimersVarious statements made in this presentation are forward-looking,within the meaning of the U.S.Private Securities Litig

2、ation Reform Act of 1995,and are inherently subject to risks,uncertainties and potentially inaccurate assumptions.All statements that address activities,events or developments that we intend,expect,plan or believe may occur in the future,are forward-looking statements,including but not limited to st

3、atements regarding:our expectations regarding our clinical development and regulatory plans;our belief that DURAVYUis on track to be the first-to-market of the current investigational sustained release treatments for wet AMD;our belief that DURAVYU has two potential blockbuster indications;our belie

4、f that DURAVYU is the only TKI in development for DME;our belief that DURAVYU is uniquely positioned to potentially address both VEGF-mediated vascular leakage and IL-6 mediated inflammatory drivers of DME as a sustained delivery therapy;our belief that DURAVYUs potential real-world application in m

5、ultiple retinal disease indications and de-risked trial designs position DURAVYU for clinical and commercial success;our expectations regarding timing for commencement of DME clinical trial enrollment and the timing of the availability and release of wet AMD clinical data;our expected cash runway;ou

6、r belief that DURAVYU has the potential to maintain a majority of patients with active disease with no supplemental anti-VEGF therapy for six months or longer;our expectations regarding our manufacturing capabilities;and our expectations regarding the timing and clinical development of our other pro

word格式文档无特别注明外均可编辑修改,预览文件经过压缩,下载原文更清晰!
三个皮匠报告文库所有资源均是客户上传分享,仅供网友学习交流,未经上传用户书面授权,请勿作商用。
1. **核心产品与进展**:DURAVYU(vorolanib玻璃体体内植入物)处于III期临床,用于湿年龄相关性黄斑变性(wet AMD)和糖尿病性黄斑水肿(DME),预计wet AMD顶线数据2026年中公布,DME III期试验2026年Q1启动。 2. **市场定位**:wet AMD和DME全球市场规模超150亿美元,DURAVYU定位为首个且唯一在研的TKI疗法,具有6个月持久性及多机制(抗VEGF、抗PDGF、抗IL-6)优势。 3. **财务与制造**:现金储备约3亿美元,支撑运营至2027年Q4;美国马萨诸塞州先进制造设施已投产。 4. **临床数据**:II期试验显示,DURAVYU可减少80%以上治疗负担,63%-88%患者6个月内无需补充抗VEGF注射,安全性良好(无相关严重不良事件)。
**DURAVYU前景如何?** **湿AMD疗法有何突破?** **DME治疗新选择?**
客服
商务合作
小程序
服务号
折叠