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(Nasdaq: ARVN) 今日宣佈,包括臨床數據在內的三份關於vepdegestrant的海報將於2024年12月10日至13日在德克薩斯州聖安東尼奧舉辦的2024年聖安東尼奧乳腺癌研討會(SABCS)上展示。vepdegestrant是一種新型的調控蛋白質降解荷爾蒙受體(ER)的藥物,由arvinas和輝瑞聯合開發,用於治療早期、局部晚期或轉移性雌激素受體陽性/人表皮生長因子受體2(HER2)陰性(ER+/HER2-)乳腺癌患者。
Poster session details are as follows:
海報展覽會詳細信息如下:
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Vepdegestrant, 一種PROTAC雌激素受體(ER)降解劑, 與CDK4/6抑制劑抗藥性Wt ER和ER Y537S突變患者來源的異體移植模型(PDX)中Palbociclib的聯合應用
海報會議3(ID: P3-01-16)
日期: 12月12日星期四
時間: 中部時間下午12:30 - 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,一種蛋白質降解靶向嵌合物(PROTAC)雌激素受體(ER)降解物,加上Abemaciclib用於ER-Pos/人類表皮生長因子受體2(HER2)陰性晚期或轉移性乳腺癌:TACTIVE-U初期10億階段結果
海報會議4 (ID: P4-12-03)
日期: 12月12日星期四
時間:下午5:30 – 7:00中部時間
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CYP3A4介導的與Vepdegestrant聯合使用時的藥物相互作用風險,一種蛋白質降解靶向嵌合物(PROTAC)雌激素受體(ER)降解物,與Cyclin Dependent Kinase (CDK)4/6抑制劑和Everolimus聯合使用
海報會議4 (ID: P4-08-13)
日期: 12月12日星期四
時間:下午5:30 – 7:00中部時間
For copies of the abstracts, please visit the official SABCS website here.
如需摘要的副本,請訪問官方SABCS網站這裏。
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是一種正在研究中的口服可用的PROTAC蛋白質降解劑,旨在有針對性地靶向並分解雌激素受體(ER),用於治療ER陽性(ER+/HER2-)乳腺癌患者。Vepdegestrant正在作爲潛在獨立治療和作爲針對 ER+/HER2-轉移性乳腺癌的多種治療方案的一部分進行開發。
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,Arvinas宣佈與輝瑞全球合作,共同開發和商業化vepdegestrant ;Arvinas和Pfizer將共同分享全球開發成本、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)授予vepdegestrant單用療法治療曾接受內分泌治療的ER陽性/HER2陰性轉移性乳腺癌成年患者快速跟蹤認證。
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:ARVN)是一家臨床階段的生物技術公司,致力於改善患有嚴重和危及生命的疾病的患者生活。通過其PROTAC(PROteolysis TArgeting Chimera)蛋白降解平台,該公司正在開拓蛋白質降解療法的發展,旨在利用人體天然蛋白質清除系統,選擇性和高效地降解和清除導致疾病的蛋白質。Arvinas目前正在推進多個處於臨床開發階段的研究藥物,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患者的BCL6的ARV-393;以及針對神經退行性疾病中LRRK2的ARV-102。Arvinas總部位於康涅狄格州紐黑文。有關Arvinas的更多信息,請訪問其網站,並在LinkedIn和X上關注。
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.
前瞻性聲明
本新聞稿包含根據1995年《私人證券訴訟改革法案》中定義的前瞻性聲明,涉及輝瑞賽諾吉(vepdegestrant)作爲單藥或作爲聯合療法的潛力,可能用於治療ER+/HER2-轉移性乳腺癌患者的聲明。關於arvinas的策略、未來運營、未來財務狀況、未來收入、預計成本、前景、計劃和管理目標的聲明都屬於前瞻性聲明。"預期,""相信,""估計,""期望,""打算,""可能,""或許,""計劃,""預測,""項目,""目標,""潛力,""將,""可能,""應,""將繼續"和類似表達旨在識別前瞻性聲明,儘管並非所有前瞻性聲明都包含這些識別詞。
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實際上可能無法實現這些前瞻性聲明中披露的計劃、意圖或期望,您不應過度依賴此類前瞻性聲明。由於各種風險和不確定性,包括但不限於:arvinas和輝瑞就輝瑞與arvinas合作履行各自義務的表現;arvinas和輝瑞是否能夠成功開展和完成vepdegestrant的臨床開發;arvinas和輝瑞是否能夠獲得vepdegestrant的營銷批准並按照現有時間表或完全商業化;arvinas保護其知識產權組合的能力;arvinas的現金及現金等價物資源是否足以支持其可預見和不可預見的營業費用和資本支出需求,以及在arvinas2023年12月31日結束的10-k表格中「風險因素」部分和美國證交會文件倉庫中隨後的其他報告中討論的其他重要因素。本新聞稿中包含的前瞻性聲明反映了arvinas對未來事件的看法,arvinas假設不會受適用法律的規定限制而更新任何前瞻性聲明。不應依賴這些前瞻性聲明來代表arvinas在本公告發布日期之後的任何日期的觀點。
Contacts
Investors:
Jeff Boyle
+1 (347) 247-5089
Jeff.Boyle@arvinas.com
聯繫方式
投資者:
Jeff Boyle
+1 (347) 247-5089
Jeff.Boyle@arvinas.com
Media:
Kirsten Owens
+1 (203) 584-0307
Kirsten.Owens@arvinas.com
媒體:
Kirsten Owens
+1 (203) 584-0307
Kirsten.Owens@arvinas.com
譯文內容由第三人軟體翻譯。