Arvinas Announces Upcoming Vepdegestrant Poster Presentations at the 2024 San Antonio Breast Cancer Symposium
Arvinas Announces Upcoming Vepdegestrant Poster Presentations at the 2024 San Antonio Breast Cancer Symposium
NEW HAVEN, Conn., Nov. 25, 2024 (GLOBE NEWSWIRE) -- Arvinas, Inc. (Nasdaq: ARVN) today announced that three posters for vepdegestrant, including clinical data, will be presented at the 2024 San Antonio Breast Cancer Symposium (SABCS), being held December 10-13, 2024, in San Antonio, Texas. Vepdegestrant is a novel investigational PROTAC estrogen receptor (ER) degrader that is being jointly developed by Arvinas and Pfizer for the treatment of patients with early and locally advanced or metastatic estrogen receptor positive/human epidermal growth factor receptor 2 (HER2) negative (ER+/HER2-) breast cancer.
康涅狄格州紐黑文,2024年11月25日(GLOBE NEWSWIRE)——Arvinas公司(納斯達克股票代碼:ARVN)今天宣佈,將在2024年12月10日至13日在德克薩斯州聖安東尼奧舉行的2024年聖安東尼奧乳腺癌研討會(SABCS)上發佈包括臨床數據在內的三張vepdegestrant海報,包括臨床數據。Vepdegestrant是一種新的在研PROTAC雌激素受體(ER)降解劑,由Arvinas和輝瑞聯合開發,用於治療早期和局部晚期或轉移性雌激素受體陽性/人類表皮生長因子受體2(HER2)陰性(ER+/HER2-)乳腺癌患者。
Poster session details are as follows:
海報會議詳情如下:
Poster Title: Evaluation of the Combination of Vepdegestrant, a PROTAC Estrogen Receptor (ER) Degrader, Plus Palbociclib in CDK4/6 Inhibitor-Resistant WT ER and ER Y537S Mutant Patient Derived Xenograft (PDX) Models
Poster Session 3 (ID: P3-01-16)
Date: Thursday, December 12
Time: 12:30 p.m. – 2:00 p.m. CT
海報標題:評估 PROTAC 雌激素受體 (ER) 降解劑 Vepdegestrant 和 Palbociclib 與 CDK4/6 抑制劑耐藥性 Wt ER 和 ER Y537S 突變體患者衍生異種移植 (PDX) 模型中的帕博西利布的組合
海報會議 3 (ID: P3-01-16)
日期:12月12日星期四
時間:美國中部時間下午 12:30 — 下午 2:00
Poster Title: Vepdegestrant, a PROteolysis TArgeting Chimera (PROTAC) Estrogen Receptor (ER) Degrader, Plus Abemaciclib in ER-Pos/Human Epidermal Growth Factor Receptor 2 (HER2) Negative Advanced or Metastatic Breast Cancer: TACTIVE-U Prelim Phase 1b Results
Poster Session 4 (ID: P4-12-03)
Date: Thursday, December 12
Time: 5:30 p.m. – 7:00 p.m. CT
海報標題:Vepdegestrant,一種靶向 Chimera (PROTAC) 雌激素受體 (ER) 降解劑,再加上 ERPOS/人類表皮生長因子受體 2 (HER2) 陰性晚期或轉移性乳腺癌中的 Abemaciclib:TACTIVE-U Prelim 第 10 期結果
海報發佈會 4 (ID: P4-12-03)
日期:12月12日星期四
時間:美國中部時間下午 5:30 — 晚上 7:00
Poster Title: Evaluating CYP3A4-Mediated Drug Interaction Risks for Vepdegestrant, a PROteolysis TArgeting Chimera (PROTAC) Estrogen Receptor (ER) Degrader, in Combination with Cyclin Dependent Kinase (CDK)4/6 Inhibitors and Everolimus
Poster Session 4 (ID: P4-08-13)
Date: Thursday, December 12
Time: 5:30 p.m. – 7:00 p.m. CT
海報標題:評估Vepdegestrant(一種靶向奇美拉(PROTAC)雌激素受體(ER)降解劑,與細胞週期蛋白依賴激酶(CDK)4/6抑制劑和依維莫司聯合使用的CYP3A4介導的藥物相互作用風險
海報發佈會 4 (ID: P4-08-13)
日期:12月12日星期四
時間:美國中部時間下午 5:30 — 晚上 7:00
For copies of the abstracts, please visit the official SABCS website here.
如需摘要的副本,請在此處訪問 SABCS 官方網站。
About Vepdegestrant
Vepdegestrant is an investigational, orally bioavailable PROTAC protein degrader designed to specifically target and degrade the estrogen receptor (ER) for the treatment of patients with ER positive (ER+)/human epidermal growth factor receptor 2 (HER2) negative (ER+/HER2-) breast cancer. Vepdegestrant is being developed as a potential monotherapy and as part of combination therapy across multiple treatment settings for ER+/HER2- metastatic breast cancer.
關於 Vepdegestrant
Vepdegestrant是一種正在研究的、口服生物利用的PROTAC蛋白降解劑,旨在專門靶向和降解雌激素受體(ER),用於治療急診室陽性(ER+)/人類表皮生長因子受體2(HER2)陰性(ER+/HER2-)乳腺癌患者。Vepdegestrant正在開發爲一種潛在的單一療法,也是ER+/HER2-轉移性乳腺癌多種治療環境中聯合療法的一部分。
In July 2021, Arvinas announced a global collaboration with Pfizer for the co-development and co-commercialization of vepdegestrant; Arvinas and Pfizer will share worldwide development costs, commercialization expenses, and profits.
2021年7月,阿維納斯宣佈與輝瑞進行全球合作,共同開發和共同商業化vepdegestrant;阿維納斯和輝瑞將分擔全球開發成本、商業化費用和利潤。
The U.S. Food and Drug Administration (FDA) has granted vepdegestrant Fast Track designation as a monotherapy in the treatment of adults with ER+/HER2- locally advanced or metastatic breast cancer previously treated with endocrine-based therapy.
美國食品藥品監督管理局(FDA)已將vepdegestrant Fast Track指定爲單一療法,用於治療以前曾接受過內分泌療法治療的ER+/HER2-局部晚期或轉移性乳腺癌的成年人。
About Arvinas
Arvinas (Nasdaq: ARVN) is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases. Through its PROTAC (PROteolysis TArgeting Chimera) protein degrader platform, the Company is pioneering the development of protein degradation therapies designed to harness the body's natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. Arvinas is currently progressing multiple investigational drugs through clinical development programs, including vepdegestrant, targeting the estrogen receptor for patients with locally advanced or metastatic ER+/HER2- breast cancer; ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; and ARV-102, targeting LRRK2 for neurodegenerative disorders. Arvinas is headquartered in New Haven, Connecticut. For more information about Arvinas, visit and connect on LinkedIn and X.
關於 Arvinas
Arvinas(納斯達克股票代碼:ARVN)是一家臨床階段的生物技術公司,致力於改善患有使人衰弱和危及生命的疾病的患者的生活。通過其PROTAC(Proteolysis targeting Chimera)蛋白質降解劑平台,該公司率先開發了蛋白質降解療法,旨在利用人體的天然蛋白質處置系統選擇性高效地降解和去除致病蛋白。Arvinas目前正在通過臨床開發項目研發多種在研藥物,包括針對局部晚期或轉移性ER+/HER2-乳腺癌患者的vepdegestrant;針對復發/難治性非霍奇金淋巴瘤的 ARV-393,靶向BCL6治療復發/難治性非霍奇金淋巴瘤;以及針對神經退行性疾病的 LRRK2 的 ARV-102。Arvinas總部位於康涅狄格州紐黑文。如需了解有關 Arvinas 的更多信息,請訪問並連接 LinkedIn 和 X。
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995 that involve substantial risks and uncertainties, including statements regarding the potential of vepdegestrant as a monotherapy and as part of combination therapy to potentially treat patients with ER+/HER2- metastatic breast cancer. Statements regarding Arvinas' strategy, future operations, future financial position, future revenues, projected costs, prospects, plans and objectives of management, are forward-looking statements. The words "anticipate," "believe," "estimate," "expect," "intend," "may," "might," "plan," "predict," "project," "target," "goal," "potential," "will," "would," "could," "should," "continue," and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.
前瞻性陳述
本新聞稿包含1995年《私人證券訴訟改革法》所指的前瞻性陳述,這些陳述涉及重大風險和不確定性,包括有關vepdegestrant作爲單一療法和作爲可能治療ER+/HER2-轉移性乳腺癌患者的聯合療法的一部分的潛力的陳述。有關Arvinas戰略、未來運營、未來財務狀況、未來收入、預計成本、管理前景、計劃和目標的陳述均爲前瞻性陳述。「預期」、「相信」、「估計」、「預期」、「打算」、「可能」、「計劃」、「預測」、「項目」、「目標」、「潛在」、「將」、「可能」、「應該」、「繼續」 等詞語旨在識別前瞻性陳述,儘管並非所有前瞻性陳述都包含這些識別詞。
Arvinas may not actually achieve the plans, intentions or expectations disclosed in these forward-looking statements, and you should not place undue reliance on such forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements Arvinas makes as a result of various risks and uncertainties, including but not limited to: Arvinas' and Pfizer's performance of the respective obligations with respect to Arvinas' collaboration with Pfizer; whether Arvinas and Pfizer will be able to successfully conduct and complete clinical development for vepdegestrant; whether Arvinas and Pfizer, as appropriate, will be able to obtain marketing approval for and commercialize vepdegestrant on current timelines or at all; Arvinas' ability to protect its intellectual property portfolio; whether Arvinas' cash and cash equivalent resources will be sufficient to fund its foreseeable and unforeseeable operating expenses and capital expenditure requirements, and other important factors discussed in the "Risk Factors" section of Arvinas' Annual Report on Form 10-K for the year ended December 31, 2023 and subsequent other reports on file with the U.S. Securities and Exchange Commission. The forward-looking statements contained in this press release reflect Arvinas' current views with respect to future events, and Arvinas assumes no obligation to update any forward-looking statements, except as required by applicable law. These forward-looking statements should not be relied upon as representing Arvinas' views as of any date subsequent to the date of this release.
Arvinas可能無法實際實現這些前瞻性陳述中披露的計劃、意圖或預期,您不應過分依賴此類前瞻性陳述。由於各種風險和不確定性,實際結果或事件可能與Arvinas在前瞻性陳述中披露的計劃、意圖和預期存在重大差異,包括但不限於:阿維納斯和輝瑞履行與輝瑞合作有關的各自義務的情況;Arvinas和輝瑞是否能夠成功進行和完成vepdegestrant的臨床開發;Arvinas和輝瑞是否能夠成功進行和完成vepdegestrant的臨床開發;Arvinas是否酌情和輝瑞將能夠獲得上市批准並實現商業化對當前時間表或根本不這樣認爲;Arvinas保護其知識產權投資組合的能力;Arvinas的現金和現金等價物資源是否足以爲其可預見和不可預見的運營費用和資本支出需求提供資金,以及Arvinas截至2023年12月31日止年度的10-k表年度報告的 「風險因素」 部分以及隨後存檔的其他報告中所討論的其他重要因素美國證券交易委員會。本新聞稿中包含的前瞻性陳述反映了Arvinas當前對未來事件的看法,除非適用法律要求,否則Arvinas沒有義務更新任何前瞻性陳述。在本新聞稿發佈之日之後的任何日期,都不應將這些前瞻性陳述視爲Arvinas的觀點。
Contacts
Investors:
Jeff Boyle
+1 (347) 247-5089
Jeff.Boyle@arvinas.com
聯繫人
投資者:
傑夫·博伊爾
+1 (347) 247-5089
Jeff.Boyle@arvinas.com
Media:
Kirsten Owens
+1 (203) 584-0307
Kirsten.Owens@arvinas.com
媒體:
克爾斯滕·歐文斯
+1 (203) 584-0307
Kirsten.Owens@arvinas.com
譯文內容由第三人軟體翻譯。