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Verve Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Verve Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Verve Therapeutics 在納斯達克上市規則5635(c)(4)下宣佈誘導性獎勵。
Verve Therapeutics ·  11/29 13:00

BOSTON, Nov. 29, 2024 (GLOBE NEWSWIRE) -- Verve Therapeutics, a clinical-stage company developing a new class of genetic medicines for cardiovascular disease, today announced that on November 29, 2024, the company granted equity awards to one new employee, pursuant to the company's 2024 Inducement Stock Incentive Plan, as an inducement material to such new employee entering into employment with the company in accordance with Nasdaq Listing Rule 5635(c)(4).

波士頓,2024年11月29日(GLOBE NEWSWIRE)——開發心血管疾病新基因藥物的臨床階段公司Verve Therapeutics今天宣佈,根據公司2024年的激勵股票激勵計劃,該公司於2024年11月29日向一名新員工發放了股權獎勵,以此作爲激勵此類新員工根據納斯達克上市規則5635 (c) (4) 進入公司的激勵材料)。

The employee received an aggregate of 5,330 restricted stock units (RSUs). The RSUs will vest in equal annual installments on the first four anniversaries of January 1, 2025, subject to such employee's continued service with the company on each such vesting date.

該員工共獲得5,330個限制性股票單位(RSU)。RSU將在2025年1月1日的前四個週年紀念日按年等額分期付款,前提是該員工在每個此類歸屬日期繼續在公司任職。

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 .

關於 Verve Therapeu
Verve Therapeutics, Inc.(納斯達克股票代碼:VERV)是一家處於臨床階段的公司,正在開發一種新的心血管疾病基因藥物,有可能將治療從慢性治療轉變爲單療程基因編輯藥物。該公司的主要項目 — VERVE-101、VERVE-102 和 VERVE-201 — 靶向的基因已被廣泛驗證爲降低低密度脂蛋白膽固醇 (LDL-C) 的靶標,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。VERVE-101 和 VERVE-102 旨在永久關閉肝臟中的 PCSK9 基因,最初是針對雜合子家族性高膽固醇血癥 (HeFH) 而開發的,最終用於治療仍受高低密度脂蛋白-C 水平影響的 ASCVD 患者。VERVE-201 旨在永久關閉肝臟中的 ANGPTL3 基因,最初是針對難治性高膽固醇血癥而開發的,儘管採用了最大耐受性的標準護理療法和純合子家族性高膽固醇血癥 (HoFH) 進行治療,但患者仍有較高的低密度脂蛋白 (LDL-C)。欲了解更多信息,請訪問。

Investor Contact
Jen Robinson
Verve Therapeutics, Inc.
jrobinson@vervetx.com

投資者聯繫方式
詹·羅賓遜
Verve Thareutics, Inc
jrobinson@vervetx.com

Media Contact
Ashlea Kosikowski
1AB
ashlea@1abmedia.com

媒體聯繫人
Ashlea Kosikowski
1AB
ashlea@1abmedia.com


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