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Monte Rosa Therapeutics Presents Preclinical Data Highlighting Potential of GSPT1-directed Molecular Glue Degrader MRT-2359 to Target Myc-driven Cancers at AACR Annual Meeting 2022

Monte Rosa Therapeutics Presents Preclinical Data Highlighting Potential of GSPT1-directed Molecular Glue Degrader MRT-2359 to Target Myc-driven Cancers at AACR Annual Meeting 2022

蒙特羅薩治療公司在AACR 2022年年會上展示臨牀前數據,強調GSPT1指導的分子膠降解劑MRT-2359針對Myc驅動癌症的潛力
GlobeNewswire ·  2022/04/09 01:07

– Data Highlight Essential Role of GSPT1 in Sustaining Myc-induced Translational Addiction in Solid Tumors –

-數據強調GSPT1在實體腫瘤中維持Myc誘導的翻譯成癮中的關鍵作用-

BOSTON, April 08, 2022 (GLOBE NEWSWIRE) -- Monte Rosa Therapeutics, Inc. (NASDAQ: GLUE), a biotechnology company developing novel molecular glue degrader (MGD)-based medicines, today announced preclinical data underscoring the role of GSPT1 as a key regulator of protein translation in Myc-driven tumors and highlighting MRT-2359 as a potent and selective GSPT1-directed MGD. The data will be presented in a poster presentation titled, "Identification of MRT-2359, a Potent, Selective and Orally Bioavailable GSPT1-directed Molecular Glue Degrader (MGD) for the Treatment of Cancers with Myc-induced Translational Addiction," at the American Association for Cancer Research (AACR) Annual Meeting in New Orleans.

波士頓,2022年4月8日(環球網)--蒙特羅莎治療公司(納斯達克:GLUE)是一家開發新型分子膠降解劑(MGD)藥物的生物技術公司,該公司今天公佈了臨牀前數據,強調了GSPT1在Myc驅動的腫瘤中作為蛋白質翻譯關鍵調節因子的作用,並強調MRT-2359是一種有效的、選擇性的GSPT1指導的MGD。這些數據將在新奧爾良舉行的美國癌症研究協會(AACR)年會上以海報形式展示,題為“鑑定MRT-2359,一種有效的、選擇性的、口服生物可用的GSPT1導向的分子膠降解劑(MGD),用於治療患有Myc誘導的翻譯成癮的癌症”。

"Myc transcription factors are well-established drivers of human cancers, and our analyses of real-world molecular and genomic data of more than 3,000 lung cancer samples continue to underscore their role as some of the most frequently mutated, translocated and overexpressed oncogenes," said Owen Wallace, Ph.D., Chief Scientific Officer of Monte Rosa. "To sustain uncontrolled cell proliferation and tumor growth, Myc-driven tumors hijack critical components of the translational machinery – including the translational termination factor GSPT1 – providing, in turn, a unique opportunity for therapeutic intervention. Our presentation at AACR represents the culmination of extensive and compelling preclinical in vivo data demonstrating the therapeutic potential of MRT-2359 as a potent, highly selective degrader of GSPT1. We look forward to submitting our IND for MRT-2359 in mid-2022."

MonteRosa首席科學官歐文·華萊士博士説:“Myc轉錄因子是人類癌症的公認驅動因素,我們對3000多個肺癌樣本的真實世界分子和基因組數據的分析繼續強調它們是一些最頻繁突變、易位和過度表達的癌基因。為了維持不受控制的細胞增殖和腫瘤生長,Myc驅動的腫瘤劫持了翻譯機制的關鍵組件-包括翻譯終止因子GSPT1-反過來提供了一個獨特的治療幹預機會。我們在AACR上的報告代表了廣泛和引人注目的臨牀前研究的頂峯體內顯示MRT-2359作為GSPT1的高效、高選擇性降解劑的治療潛力的數據。我們期待着在2022年年中提交我們的MRT-2359 IND。“

Summary of Findings
The data being presented at the AACR meeting are based on preclinical studies and analyses of real-world data derived from patient tumor samples. Findings include the following:

調查結果摘要
在AACR會議上提交的數據是基於臨牀前研究和對來自患者腫瘤樣本的真實數據的分析。調查結果包括以下幾點:

  • MRT-2359 induces degradation of GSPT1 and associated downregulation of N-Myc and its transcriptional output, leading to preferential anti-proliferative activity in lung cancer cell lines with high L-Myc and N-Myc mRNA expression.
  • MRT-2359, when administered orally, demonstrates anti-tumor activity in xenograft and patient-derived xenograft (PDX) models of non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) with high L-Myc and/or N-Myc mRNA expression levels or neuroendocrine features.
  • MRT-2359 had limited activity in low L-Myc or N-Myc NSCLC models, further corroborating the selective vulnerability of Myc-driven tumors to GSPT1 degradation.
  • Analyses of real-world data indicate that approximately 15% of NSCLC and 70% of SCLC have high L-Myc and/or N-Myc mRNA expression.
  • Collectively, these data support the clinical development of MRT-2359 in Myc-driven solid tumors, with an initial focus on NSCLC and SCLC.
  • MRT-2359可誘導GSPT1的降解和N-Myc及其轉錄產物的下調,導致高表達L-Myc和N-Myc的肺癌細胞株具有優先的抗增殖活性。
  • 口服時,MRT-2359在非小細胞肺癌(NSCLC)和小細胞肺癌(SCLC)的異種移植和患者來源的異種移植(PDX)模型中顯示出抗腫瘤活性,這些模型具有高L-Myc和/或N-Myc mRNA表達水平或神經內分泌特徵。
  • MRT-2359在低L-Myc或N-Myc NSCLC模型中活性有限,進一步證實了Myc驅動的腫瘤對GSPT1降解的選擇性脆弱性。
  • 對真實世界數據的分析表明,大約15%的非小細胞肺癌和70%的小細胞肺癌具有高水平的L-Myc和/或N-Myc mRNA表達。
  • 總的來説,這些數據支持MRT-2359在Myc驅動的實體腫瘤中的臨牀開發,最初的重點是非小細胞肺癌和小細胞肺癌。

About Monte Rosa
Monte Rosa Therapeutics is a biotechnology company developing a portfolio of novel molecular glue degrader medicines. These medicines are designed to employ the body's natural mechanisms to selectively eliminate therapeutically relevant proteins. The company has developed a proprietary protein degradation platform, called QuEEN™ (Quantitative and Engineered Elimination of Neosubstrates), that enables it to rapidly identify protein targets and molecular glue degrader, or MGD, product candidates that are designed to eliminate therapeutically relevant proteins in a highly selective manner. The company's drug discovery platform combines diverse and proprietary chemical libraries of small molecule protein degraders with in-house proteomics, structural biology, AI/machine learning-based target selection and computational chemistry capabilities to predict and obtain protein degradation profiles. For more information, visit . 

關於蒙特羅莎
蒙特羅莎治療公司是一家生物技術公司,正在開發一系列新型分子膠降解劑藥物組合。這些藥物旨在利用人體的自然機制選擇性地消除與治療相關的蛋白質。該公司開發了一種專有的蛋白質降解平臺,名為皇后™(曲目反義ANDE工程學E限制N這使其能夠快速識別蛋白質靶標和分子膠降解劑(MGD),這些候選產品旨在以高度選擇性的方式消除與治療相關的蛋白質。該公司的藥物發現平臺將各種專有的小分子蛋白質降解物化學庫與內部蛋白質組學、結構生物學、基於人工智能/機器學習的目標選擇和計算化學能力相結合,以預測和獲得蛋白質降解情況。有關更多信息,請訪問。

Forward-Looking Statements
This communication includes express and implied "forward-looking statements," including forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include all statements that are not historical facts, and in some cases, can be identified by terms such as "may," "might," "will," "could," "would," "should," "expect," "intend," "plan," "objective," "anticipate," "believe," "estimate," "predict," "potential," "continue," "ongoing," or the negative of these terms, or other comparable terminology intended to identify statements about the future. Forward-looking statements contained herein include, but are not limited to, statements about our product development activities, including our expectations around the ongoing development of our QuEEN™ platform, the advancement of our pipeline and the various products therein, including our expectations of timing for filing our IND for our GSPT1-directed molecular glue degrader, MRT-2359, the advancement of additional programs including NEK7 and CDK2, the expansion of our compound and degron libraries, our ability to initiate at least one additional lead optimization programs, our ability to identify additional molecular glue degraders, our scientific predictions around clinical opportunities for our programs, including for MRT-2359, and any of our statements about the progress, results, costs, predictions, and our expectations for our molecular glue degraders, including for MRT-2359. By their nature, these statements are subject to numerous risks and uncertainties, including the impact that the current COVID-19 pandemic will have on our development activities and operations, as well as those risks and uncertainties set forth in our Annual Report on Form 10-K for the fourth quarter and full year ended December 31, 2021, filed with the US Securities and Exchange Commission on March 29, 2022, and any subsequent filings, that could cause actual results, performance or achievement to differ materially and adversely from those anticipated or implied in the statements. You should not rely upon forward-looking statements as predictions of future events. Although our management believes that the expectations reflected in our statements are reasonable, we cannot guarantee that the future results, performance or events and circumstances described in the forward-looking statements will be achieved or occur. Recipients are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date such statements are made and should not be construed as statements of fact. We undertake no obligation to publicly update any forward-looking statements, whether as a result of new information, any future presentations or otherwise, except as required by applicable law. Certain information contained in these materials and any statements made orally during any presentation of these materials that relate to the materials or are based on studies, publications, surveys and other data obtained from third-party sources and our own internal estimates and research. While we believe these third-party studies, publications, surveys and other data to be reliable as of the date of these materials, it has not been independently verified and makes no representations as to the adequacy, fairness, accuracy or completeness of any information obtained from third-party sources. In addition, no independent source has evaluated the reasonableness or accuracy of our internal estimates or research and no reliance should be made on any information or statements made in these materials relating to or based on such internal estimates and research. 

前瞻性陳述
這一溝通包括明示和暗示的“前瞻性陳述”,包括1995年“私人證券訴訟改革法”所指的前瞻性陳述。前瞻性陳述包括所有不是歷史事實的陳述,在某些情況下,可以用“可能”、“可能”、“將會”、“可能”、“將會”、“應該”、“預期”、“打算”、“計劃”、“目標”、“預期”、“相信”、“估計”、“預測”、“潛在”、“繼續”、“正在進行”、“或這些術語的否定,或旨在識別關於未來的陳述的其他可比術語。本文包含的前瞻性陳述包括但不限於對我們的產品開發活動的陳述,包括我們對皇后™平臺正在進行的開發的期望、我們流水線和其中各種產品的進展,包括我們對為我們的GSPT1定向分子膠降解器MRT-2359提交IND的時間的預期、包括NEK7和CDK2在內的其他計劃的進展、我們化合物和降解庫的擴展、我們啟動至少一個額外的先導優化計劃的能力、我們識別其他分子膠降解劑的能力、我們對我們計劃的臨牀機會的科學預測。包括MRT-2359,以及我們對包括MRT-2359在內的分子膠降解器的進度、結果、成本、預測和期望的任何陳述。就其性質而言,這些聲明會受到許多風險和不確定性的影響,包括當前的新冠肺炎疫情將對我們的開發活動和運營產生的影響,以及我們在提交給美國證券交易委員會的截至2021年12月31日的第四季度和全年的Form 10-K年度報告中闡述的風險和不確定性, 以及任何隨後提交的文件,可能導致實際結果、業績或成就與聲明中預期或暗示的結果、業績或成就大不相同。你不應該依賴前瞻性陳述作為對未來事件的預測。儘管我們的管理層認為我們的陳述中反映的預期是合理的,但我們不能保證前瞻性陳述中描述的未來結果、業績或事件和情況將會實現或發生。提醒收件人不要過度依賴這些前瞻性陳述,這些陳述僅反映了此類陳述發表之日,不應被解釋為事實陳述。我們沒有義務公開更新任何前瞻性陳述,無論是由於新信息、任何未來陳述或其他原因,除非適用法律要求。這些材料中包含的某些信息以及在這些材料的任何陳述過程中所作的任何口頭陳述,涉及這些材料或基於從第三方來源獲得的研究、出版物、調查和其他數據以及我們自己的內部估計和研究。雖然我們認為這些第三方研究、出版物、調查和其他數據截至這些材料的日期是可靠的,但它尚未經過獨立核實,也沒有就從第三方來源獲得的任何信息的充分性、公平性、準確性或完整性做出任何陳述。此外,並無獨立消息來源評估本公司內部估計或研究的合理性或準確性,亦不應依賴該等材料中與該等內部估計及研究有關或基於該等內部估計及研究而作出的任何資料或陳述。

Contacts:

聯繫人:

Investors
Michael Morabito, Solebury Trout
ir@monterosatx.com

投資者
邁克爾·莫拉比託,索爾伯裏鮭魚
郵箱:ir@monterosatx.com

Media
Dan Budwick, 1AB
dan@1abmedia.com

媒體
丹·巴德威克,1AB
電子郵箱:Dan@1abmedia.com


譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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