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Evaxion Presents Positive and Validating Immune Data From Ongoing Phase 2 Trial With AI-Designed EVX-01 Vaccine at the ASCO Annual Meeting 2024

Evaxion Presents Positive and Validating Immune Data From Ongoing Phase 2 Trial With AI-Designed EVX-01 Vaccine at the ASCO Annual Meeting 2024

Evaxion在2024年ASCO年會上介紹了人工智能設計的EVX-01生物-疫苗正在進行的二期試驗積極且有效的免疫數據。
Evaxion Biotech ·  06/03 12:00
  • Evaxion's AI-designed cancer vaccine, EVX-01, triggered a specific and tumor-targeting immune response in all assayed melanoma patients
  • Findings further confirm and validate the precision and predictive power of Evaxion's AI vaccine target discovery and design platform, AI-Immunology
  • Evaxion 的人工智能設計的癌症疫苗 EVX-01 在所有接受檢測的黑色素瘤患者中觸發了針對腫瘤的特異性免疫反應
  • 研究結果進一步證實並驗證了Evaxion的人工智能疫苗靶點發現和設計平台AI-Immunology的精度和預測能力

COPENHAGEN, Denmark, June 03, 2024 (GLOBE NEWSWIRE) -- Evaxion Biotech A/S (NASDAQ: EVAX) ("Evaxion" or the "Company"), a clinical-stage TechBio company specializing in developing AI-Immunology powered vaccines, reported data from its ongoing Phase 2 study at the American Society of Clinical Oncology (ASCO) Annual Meeting 2024. The data demonstrated vaccine-induced immune response in metastatic melanoma patients treated with the Company's AI-Immunology designed personalized cancer vaccine, EVX-01, in combination with an anti-PD1 inhibitor. The EVX-01 vaccine targets neoantigens - antigenic sequences derived from cancer mutations - that are displayed on the surface of the cancer cells, allowing the immune system to recognize, attack and eliminate the malignant cells.

丹麥哥本哈根,2024年6月3日(環球新聞專線)——專門開發人工智能免疫疫苗的臨床階段TechBio公司Evaxion Biotech A/S(納斯達克股票代碼:EVAX)(“Evaxion” 或 “公司”)在2024年美國臨床腫瘤學會(ASCO)年會上報告了正在進行的2期研究的數據。數據顯示,在使用該公司人工智能免疫學設計的個性化癌症疫苗 EVX-01 和抗PD1抑制劑治療的轉移性黑色素瘤患者中,疫苗會誘發免疫反應。EVX-01 疫苗靶向顯示在癌細胞表面的新抗原(源自癌症突變的抗原序列),使免疫系統能夠識別、攻擊和消滅惡性細胞。

"We believe these positive data further confirms the precision and predictive power of our AI-Immunology platform. This analysis shows the potential of EVX-01 and our AI platform's ability to develop life-saving and life-improving treatments. We look forward to the one-year clinical readout in the third quarter of 2024 and are excited about the interest we are seeing in EVX-01," said Christian Kanstrup, CEO of Evaxion.

“我們認爲,這些積極的數據進一步證實了我們的人工智能免疫學平台的精度和預測能力。該分析顯示了 EVX-01 的潛力以及我們的 AI 平台開發挽救生命和改善生活的治療方法的能力。我們期待在2024年第三季度公佈爲期一年的臨床數據,並對我們對 EVX-01 的興趣感到興奮。” Evaxion首席執行官克里斯蒂安·坎斯特魯普說。

Key EVX-01 Phase 2 study findings presented at the meeting:

會議上介紹的 EVX-01 第 2 階段研究的關鍵:

  • The EVX-01 vaccine induced specific and targeted immune responses, with 71% of the administered neoantigens eliciting a T-cell response
  • The neoantigen-reactive immune responses were mediated by both CD4+ and CD8+ T-cells
  • EVX-01 booster immunizations tended to increase the immune responses and did not impose any safety concerns
  • A statistically significant positive correlation between neoantigen quality, as predicted by AI-Immunology, and vaccine-induced immune response was demonstrated
  • The EVX-01 vaccine candidate was found to be well-tolerated, with only grade 1 and 2 adverse events
  • EVX-01 疫苗可誘導特異性和靶向免疫反應,71% 的新抗原引發 T 細胞反應
  • 新抗原反應性免疫反應由 CD4+ 和 CD8+ T 細胞介導
  • EVX-01 加強免疫接種往往會增加免疫反應,不會帶來任何安全問題
  • 正如人工智能免疫學所預測的那樣,新抗原質量與疫苗誘導的免疫反應之間存在統計學上的顯著正相關性
  • EVX-01 候選疫苗被發現耐受性良好,只有 1 級和 2 級不良事件

The data presented from the Phase 2 study currently confirm findings from the previous EVX-01 Phase 1 study, reaffirming the ability of Evaxion's AI-Immunology platform to precisely select therapeutically relevant vaccine targets. The Phase 2 study is ongoing and continues to generate new valuable insights.

目前,2期研究提供的數據證實了先前的 EVX-01 1期研究的結果,重申了Evaxion的人工智能免疫學平台精確選擇與治療相關的疫苗靶標的能力。第二階段研究正在進行中,並將繼續產生新的有價值的見解。

About EVX-01 Phase 2 Clinical Trial

關於 EVX-01 2 期臨床試驗

EVX-01 is Evaxion's lead clinical asset and constitutes a peptide-based personalized cancer vaccine. The ongoing Phase 2 clinical study is a self-sponsored, open-label, single-arm, multi-center trial carried out in collaboration with Merck Sharp & Dohme LLC, together with leading principal investigators and research centers from Italy and Australia. It aims to evaluate the efficacy and safety of EVX-01 vaccination in combination with the anti-PD1 treatment pembrolizumab (more commonly known as KEYTRUDA) in treatment-naive patients with metastatic or unresectable malignant stage III or IV melanoma. More information can be accessed under clinical trial ID NCT05309421.

EVX-01 是 Evaxion 的主要臨床資產,是一種基於肽的個性化癌症疫苗。正在進行的2期臨床研究是一項自發贊助、開放標籤、單臂、多中心試驗,與默沙東夏普和多姆有限責任公司以及來自意大利和澳大利亞的主要研究人員和研究中心合作開展。它旨在評估 EVX-01 疫苗接種與抗 PD1 療法 pembrolizumab(通常稱爲 KEYTRUDA)聯合使用的療效和安全性)用於未接受治療的轉移性或不可切除的惡性III期或IV期黑色素瘤患者。可以在臨床試驗 ID 下訪問更多信息 NCT05309421

About EVAXION

關於 EVAXION

Evaxion Biotech A/S is a pioneering TechBio company based upon its AI platform, AI-Immunology. Evaxion's proprietary and scalable AI prediction models harness the power of artificial intelligence to decode the human immune system and develop novel immunotherapies for cancer, bacterial diseases, and viral infections. Based upon AI-Immunology, Evaxion has developed a clinical-stage oncology pipeline of novel personalized vaccines and a preclinical infectious disease pipeline in bacterial and viral diseases with high unmet medical needs. Evaxion is committed to transforming patients' lives by providing innovative and targeted treatment options. For more information about Evaxion and its groundbreaking AI-Immunology platform and vaccine pipeline, please visit our website.

Evaxion Biotech A/S是一家基於其人工智能平台AI免疫學的開創性TechBio公司。Evaxion 專有且可擴展的人工智能預測模型利用人工智能的力量來解碼人體免疫系統,開發針對癌症、細菌性疾病和病毒感染的新型免疫療法。基於人工智能免疫學,Evaxion開發了臨床階段的新型個性化疫苗腫瘤產品線,以及針對未滿足大量醫療需求的細菌和病毒性疾病的臨床前傳染病管線。Evaxion致力於通過提供創新的有針對性的治療方案來改變患者的生活。如需了解有關 Evaxion 及其開創性的人工智能免疫學平台和疫苗管道的更多信息,請 訪問我們的網站

Forward-Looking Statement

前瞻性陳述

This announcement contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. The words "target," "believe," "expect," "hope," "aim," "intend," "may," "might," "anticipate," "contemplate," "continue," "estimate," "plan," "potential," "predict," "project," "will," "can have," "likely," "should," "would," "could," and other words and terms of similar meaning identify forward-looking statements. Actual results may differ materially from those indicated by such forward-looking statements as a result of various factors, including, but not limited to, risks related to: our financial condition and need for additional capital; our development work; cost and success of our product development activities and preclinical and clinical trials; commercializing any approved pharmaceutical product developed using our AI platform technology, including the rate and degree of market acceptance of our product candidates; our dependence on third parties including for conduct of clinical testing and product manufacture; our inability to enter into partnerships; government regulation; protection of our intellectual property rights; employee matters and managing growth; our ADSs and ordinary shares, the impact of international economic, political, legal, compliance, social and business factors, including inflation, and the effects on our business from the worldwide ongoing COVID-19 pandemic and the ongoing conflict in the region surrounding Ukraine and Russia and the Middle East; and other uncertainties affecting our business operations and financial condition. For a further discussion of these risks, please refer to the risk factors included in our most recent Annual Report on Form 20-F and other filings with the U.S. Securities and Exchange Commission (SEC), which are available at www.sec.gov. We do not assume any obligation to update any forward-looking statements except as required by law.

本公告包含經修訂的1933年《證券法》第27A條和經修訂的1934年《證券交易法》第21E條所指的前瞻性陳述。“目標”、“相信”、“期望”、“希望”、“目標”、“打算”、“可能”、“預測”、“考慮”、“繼續”、“估計”、“計劃”、“潛力”、“預測”、“項目”、“將會”、“可能”、“可能”、“應該”、“會”、“可能” 等詞語具有相似含義的術語用於識別前瞻性陳述。由於各種因素,實際結果可能與此類前瞻性陳述所示結果存在重大差異,包括但不限於以下方面的風險:我們的財務狀況和對額外資本的需求;我們的開發工作;我們的產品開發活動以及臨床前和臨床試驗的成本和成功;使用我們的人工智能平台技術開發的任何經批准的藥品的商業化,包括候選產品的市場接受率和程度;我們對第三方的依賴,包括進行臨床測試和產品製造;我們無法建立合作伙伴關係;政府監管;保護我們的知識產權;員工事務和管理增長;我們的ADS和普通股,包括通貨膨脹在內的國際經濟、政治、法律、合規、社會和商業因素的影響,以及全球持續的 COVID-19 疫情以及烏克蘭、俄羅斯和中東周邊地區的持續衝突對我們業務的影響;以及影響我們業務的其他不確定性運營和財務狀況。有關這些風險的進一步討論,請參閱我們最新的20-F表年度報告和向美國證券交易委員會(SEC)提交的其他文件中包含的風險因素,這些文件可在以下網址查閱 www.sec.gov。除非法律要求,否則我們不承擔任何更新任何前瞻性陳述的義務。

Contact Information Evaxion Biotech A/S Christian Kanstrup Chief Executive Officer cka@evaxion-biotech.com Source: Evaxion Biotech

聯繫信息 Evaxion Biotech A/S Christian Kanstrup 首席執行官 cka@evaxion-biotech.com 來源:Evaxion Biotech

譯文內容由第三人軟體翻譯。


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