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Nuvalent, Inc. (NUVL)

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70.65+1.77 (+2.57%)
收市:04:00PM EDT
70.65 +0.10 (+0.14%)
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Nuvalent, Inc.

One Broadway
14th Floor
Cambridge, MA 02142
United States
857 357 7000
https://www.nuvalent.com

版塊Healthcare
行業Biotechnology
全職員工92

高階主管

名稱頭銜支付行使價出生年份
Dr. James R. Porter Ph.D.CEO, President & Director998.02k1976
Prof. Matthew D. Shair Ph.D.Founder, Head of Scientific Advisory Board & Director235k1969
Dr. Christopher D. Turner M.D.Chief Medical Officer714.26k1969
Dr. Benjamin Lane Ph.D.Senior Vice President of Technical Operations
Ms. Deborah Ann Miller J.D., Ph.D.Chief Legal Officer & Secretary595.96k1976
Mr. Matthew MetivierSenior Vice President of Human Resources
Ms. Darlene NociChief Development Officer1978
Mr. Henry Pelish Ph.D.Senior Vice President of Drug Discovery
Mr. John Soglia Ph.D.Senior Vice President of Translational Development
Ms. Perrin Wilson B.S., Ph.D.Senior Vice President of Business Development & Strategy
截止 2022年12月31日為止計算的金額,現金賠償則計算至上一個財政年度末止。薪資是指薪俸、獎金等。已行使價是指財政年度期間已行使的期權價值。貨幣為 USD。

描述

Nuvalent, Inc., a clinical stage biopharmaceutical company, engages in the development of therapies for patients with cancer. Its lead product candidates are NVL-520, a novel ROS1-selective inhibitor to address the clinical challenges of emergent treatment resistance, central nervous system (CNS)-related adverse events, and brain metastases that may limit the use of ROS1 tyrosine kinase inhibitors (TKIs) for patients with ROS proto-oncogene 1 (ROS1)-positive non-small cell lung cancer (NSCLC) which is under the phase 2 portion of the ARROS-1 Phase 1/2 clinical trial; NVL-655, a brain-penetrant ALK-selective inhibitor, to address the clinical challenges of emergent treatment resistance, CNS-related adverse events, and brain metastases that might limit the use of first-, second-, and third-generation ALK inhibitors that is under the phase 2 portion of the ALKOVE-1 Phase 1/2 clinical trial; and NVL-330, a brain-penetrant human epidermal growth factor receptor 2 (HER2)-selective inhibitor designed to treat tumors driven by HER2ex20, brain metastases, and avoiding treatment-limiting adverse events including due to off-target inhibition of wild-type EGFR, which is expected to initiate phase 1 trial. The company was incorporated in 2017 and is headquartered in Cambridge, Massachusetts.

公司管治

截至 2024年4月29日 止,Nuvalent, Inc. 的 ISS 管治質素評分為 9。 Pillar 分數正在審核中:7;董事會:7;股東權利:10;現金賠償:9。

企業管治評分的資料提供: Institutional Shareholder Services (ISS). 評分將以 1 至 10 分顯示 (與指數或地區相關)。1 分表示較低的管治風險,而 10 分表示較高的管治風險。