Verve Therapeutics to Participate in Upcoming Investor Conferences
Verve Therapeutics to Participate in Upcoming Investor Conferences
BOSTON, May 30, 2024 (GLOBE NEWSWIRE) -- Verve Therapeutics, a clinical-stage biotechnology company pioneering a new approach to the care of cardiovascular disease with single-course gene editing medicines, today announced that management will participate in fireside chats during the following investor conferences:
波士頓,2024年5月30日(GLOBE NEWSWIRE)-- Verve Therapeutics致力於利用單次基因編輯藥物開創性的新方法治療心血管疾病的一家臨床前生物技術公司——, 某某今日宣佈,管理層將參加以下投資者會議的座談會:
- Jefferies Global Healthcare Conference on Thursday, June 6, 2024, at 1 p.m. ET in New York, NY
- Goldman Sachs 45th Annual Global Healthcare Conference on Monday, June 10, 2024, at 8 a.m. ET in Miami Beach, FL
- 全球醫療健康大會將於2024年6月6日星期四美國紐約時間下午1點在紐約舉行。
- 高盛th年度全球醫療健康大會將於2024年6月10日星期一美國邁阿密海灘東部時間上午8點舉行。
Live webcasts will be available in the investor section of the company's website at www.vervetx.com, and will be archived for 30 days following the fireside chats.
公司網站的投資者版塊將提供現場網絡直播。www.vervetx.com座談會結束後,將爲期30天進行存檔。
About Verve Therapeutics
Verve Therapeutics, Inc. (Nasdaq: VERV) is a clinical-stage genetic medicines company pioneering a new approach to the care of cardiovascular disease, potentially transforming 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 homozygous familial hypercholesterolemia (HoFH) and for refractory hypercholesterolemia where patients still have high LDL-C despite treatment with maximally-tolerated standard of care therapies. For more information, please visit www.VerveTx.com.
關於Verve Therapeutics
Verve Therapeutics,Inc.(納斯達克代碼:VERV)是一家臨床階段的遺傳藥品公司,開創了一種新的心血管疾病護理方式,可能將治療從慢性管理轉變爲單次基因編輯藥品。公司的主要項目VERVE-101、VERVE-102和VERVE-201針對已被廣泛驗證爲低密度脂蛋白膽固醇(LDL-C)降低的靶點基因,這是動脈粥樣硬化性心血管疾病(ASCVD)的根本原因。VERVE-101和VERVE-102旨在永久關閉肝臟中的PCSK9基因,並首先開發用於雜合子家族性高膽固醇血癥(HeFH),最終用於治療繼續受高LDL-C水平影響的已確診ASCVD患者。VERVE-201旨在永久關閉一種受體基因,該基因的降解被認爲是促進冠狀動脈血管單位深度和體積增加的關鍵步驟,因此是一種可能的靶切點,因爲它可能降低心血管病發作的風險。
狂犬病治療的新方法可能不再需要一系列疫苗注射,因爲百思可得(Nasdaq:VERV)的基因編輯技術有望實現單次基因編輯,以消除對一些基因的惡性變異。VERV-101,VERV-102和VERV-201是百思可得的主要項目。這些項目的目標基因被廣泛認可作爲降低低密度脂蛋白膽固醇(LDL-C)的靶向基因,而低密度脂蛋白膽固醇是動脈粥樣硬化性心血管疾病(ASCVD)的根本原因之一。VERV-101和VERV-102旨在永久性關閉肝臟中的PCSK9基因,並最初爲雜合子家族性高膽固醇血癥(HeFH)的患者進行開發,並最終治療仍受高LDL-C水平影響的已確診ASCVD患者。VERV-201旨在永久性關閉肝臟中的ANGPTL3基因,並最初爲家族性高膽固醇血癥(HoFH)患者進行開發,以及爲仍有高LDL-C的refractory hypercholesterolemia患者進行治療,儘管他們已接受過最大限度耐受的標準治療。如果想了解更多信息,請訪問www.VerveTx.com.
Investor Contact
Jen Robinson
Verve Therapeutics, Inc.
jrobinson@vervetx.com
投資者聯繫方式
詹·羅賓遜
Verve Therapeutics,Inc。
jrobinson@vervetx.com
Media Contact
Ashlea Kosikowski
1AB
ashlea@1abmedia.com
媒體聯繫人
阿什莉·科西科夫斯基
1AB
ashlea@1abmedia.com