Verve Therapeutics to Present at the 43rd Annual J.P. Morgan Healthcare Conference
Verve Therapeutics to Present at the 43rd Annual J.P. Morgan Healthcare Conference
BOSTON, Jan. 08, 2025 (GLOBE NEWSWIRE) -- Verve Therapeutics, a clinical-stage company developing a new class of genetic medicines for cardiovascular disease, today announced that Sekar Kathiresan, M.D., co-founder and chief executive officer, will present at the 43rd Annual J.P. Morgan Healthcare Conference on Wednesday, January 15, 2025 at 11:15 a.m. PT in San Francisco.
波士顿,2025年1月8日(GLOBE NEWSWIRE)——开发心血管疾病新基因药物的临床阶段公司Verve Therapeutics今天宣布,联合创始人兼首席执行官Sekar Kathiresanwand.D.将于太平洋时间2025年1月15日星期三上午11点15分出席在旧金山举行的第43届摩根大通医疗年度会议。
A live webcast will be available in the investor section of the company's website at . The webcast will be archived for 30 days following the presentation.
公司网站的 “投资者” 部分将提供网络直播,网址为。网络直播将在演讲结束后存档30天。
About Verve Therapeutics
Verve Therapeutics, Inc. (Nasdaq: VERV) is a clinical-stage company developing a new class of genetic medicines for cardiovascular disease with the potential to transform treatment from chronic management to single-course gene editing medicines. The company's lead programs – VERVE-101, VERVE-102, and VERVE-201 – target genes that have been extensively validated as targets for lowering low-density lipoprotein cholesterol (LDL-C), a root cause of atherosclerotic cardiovascular disease (ASCVD). VERVE-101 and VERVE-102 are designed to permanently turn off the PCSK9 gene in the liver and are being developed initially for heterozygous familial hypercholesterolemia (HeFH) and ultimately to treat patients with established ASCVD who continue to be impacted by high LDL-C levels. VERVE-201 is designed to permanently turn off the ANGPTL3 gene in the liver and is initially being developed for refractory hypercholesterolemia, where patients still have high LDL-C despite treatment with maximally tolerated standard of care therapies, and homozygous familial hypercholesterolemia (HoFH). For more information, please visit .
关于 Verve 疗法
Verve Therapeutics, Inc.(纳斯达克股票代码:VERV)是一家处于临床阶段的公司,正在开发一种新的心血管疾病基因药物,有可能将治疗从慢性治疗转变为单疗程基因编辑药物。该公司的主要项目 — VERVE-101、VERVE-102 和 VERVE-201 — 靶向的基因已被广泛验证为降低低密度脂蛋白胆固醇 (LDL-C) 的靶标,低密度脂蛋白胆固醇是动脉粥样硬化性心血管疾病 (ASCVD) 的根本原因。VERVE-101 和 VERVE-102 旨在永久关闭肝脏中的 PCSK9 基因,最初是针对杂合子家族性高胆固醇血症 (HeFH) 而开发的,最终用于治疗仍受高低密度脂蛋白-C 水平影响的 ASCVD 患者。VERVE-201 旨在永久关闭肝脏中的 ANGPTL3 基因,最初是针对难治性高胆固醇血症而开发的,尽管采用了最大耐受性的标准护理疗法和纯合子家族性高胆固醇血症 (HoFH) 进行治疗,但患者仍有较高的低密度脂蛋白 (LDL-C)。欲了解更多信息,请访问。
Investor Contact
Jen Robinson
Verve Therapeutics, Inc.
jrobinson@vervetx.com
投资者联系方式
詹·罗宾逊
Verve Therapeutics, Inc.
jrobinson@vervetx.com
Media Contact
Ashlea Kosikowski
1AB
ashlea@1abmedia.com
媒体联系人
阿什莉亚·科西科夫斯基
1AB
ashlea@1abmedia.com