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NovAccess Global Announces New License to Advance Its Immunotherapy Platform

NovAccess Global Announces New License to Advance Its Immunotherapy Platform

NovAccess Global宣佈了推進其免疫療法平台的新許可證
Accesswire ·  04/30 21:00

CLEVELAND, OH / ACCESSWIRE / April 30, 2024 / NovAccess Global Inc. (OTCQB:XSNX), a biomedical company developing a novel immunotherapy for patients suffering from cancers of the central nervous system, today announced the procurement of a new intellectual property license from Cedars-Sinai Medical Center to further advance the Company's immunotherapy platform. The license pertains to the use of Isocitrate Dehydrogenase-1 (IDH1), a protein previously known to impact cell metabolism. The Company intends to leverage this license to predict a patient's likely response to vaccine immunotherapy during treatment for highly malignant brain tumors, such as glioblastoma.

俄亥俄州克利夫蘭/ACCESSWIRE/2024年4月30日/爲中樞神經系統癌症患者開發新型免疫療法的生物醫學公司NovAccess Global Inc.(OTCQB: XSNX)今天宣佈從Cedars-Sinai醫療中心獲得新的知識產權許可證,以進一步推進該公司的免疫療法平台。該許可證涉及異檸檬酸脫氫酶-1(IDH1)的使用,這是一種以前已知會影響細胞新陳代謝的蛋白質。該公司打算利用該許可證來預測患者在治療膠質母細胞瘤等高度惡性腦腫瘤期間可能對疫苗免疫療法的反應。

IDH1 is commonly mutated in brain and other tumors. Groundbreaking research published by Dr. Chris Wheeler, President and lead scientist of NovAccess Global's subsidiary StemVax, LLC, has shown that IDH1 predicts antitumor responses after vaccine therapy through a novel molecular mechanism. The Company assesses that IDH1 expression is likely to discern long-duration from short-duration survivors after vaccine therapy in patients with brain tumors such as glioblastoma. Information derived from the use of IDH1 as a biomarker will help to better inform therapeutic strategy as physicians assess the use of single agent or combination therapies in their treatment of patients facing these life-threatening diagnoses.

IDH1 通常在腦部和其他腫瘤中發生突變。NovAccess Global子公司StemVax, LLC總裁兼首席科學家克里斯·惠勒博士發表的開創性研究表明,IDH1通過一種新的分子機制預測疫苗治療後的抗腫瘤反應。該公司估計,在腦膠質母細胞瘤等腦腫瘤患者進行疫苗治療後,IDH1的表達可能會從短期倖存者中長期區分出來。當醫生評估在治療面臨這些危及生命的診斷的患者時使用單藥或聯合療法時,使用IDH1作爲生物標誌物獲得的信息將有助於更好地爲治療策略提供信息。

NovAccess Global intends to support the development of IDH1 as a biomarker for TRL-AD1, its candidate drug for the treatment of cancers of the central nervous system that in 2022 received Orphan Drug designation by the U.S. Food and Drug Administration (FDA). The Company will assess IDH1 as a companion diagnostic to TRL-AD1 while exploring IDH1's potential to serve as a prognostic indicator of patient response to currently marketed therapies and those in clinical development.

NovAccess Global打算支持開發IDH1作爲 TRL-AD1 的生物標誌物。是其治療中樞神經系統癌症的候選藥物,於2022年獲得美國食品藥品監督管理局(FDA)的孤兒藥認定。該公司將評估 IDH1 作爲 TRL-AD1 的伴隨診斷,同時探索 IDH1 作爲患者對當前上市療法和臨床開發療法反應的預後指標的潛力。

"Dr. Wheeler's research continues to lead the industry and is incredibly important to the advancement of our immunotherapy platform for brain tumor treatment and potentially for other cancer therapies," said NovAccess Global's Chief Executive Officer Dr. Dwain K. Irvin. "In particular, we anticipate his findings from work with IDH1 will complement NovAccess' TLR-AD1 vaccine approach by allowing selection of the most suitable patients for treatment and thereby maximizing the treatment's benefits to them. This combination represents a potentially significant breakthrough toward achieving improved outcomes and enhanced life expectancy for those suffering from brain cancer, which may bring relief to many of the approximately 10,000 people per year in America alone dying from this condition."

NovAccess Global首席執行官德溫·歐文博士表示:“惠勒博士的研究繼續處於行業領先地位,對於我們腦腫瘤治療乃至其他癌症療法的免疫療法平台的發展至關重要。”“特別是,我們預計他在與IDH1合作中得出的發現將補充NovAccess的 TLR-AD1 疫苗方法,允許選擇最適合治療的患者,從而最大限度地提高治療對他們的益處。這種組合代表着在改善腦癌患者預後和延長其預期壽命方面可能取得的重大突破,這可能會使僅在美國每年死於這種疾病的約10,000人中的許多人得到緩解。”

Cedars-Sinai Medical Center, where Drs. Wheeler and Irvin previously collaborated in optimizing brain tumor vaccines, owns the patent for IDH1's use as a predictor of brain tumor vaccine success, and is granting an exclusive license for that use to StemVax Therapeutics.

惠勒博士和歐文博士此前曾在錫達斯-西奈醫療中心合作優化腦腫瘤疫苗,該中心擁有IDH1用作腦腫瘤疫苗成功預測指標的專利,並正在向StemVax Therapeutics授予該用途的獨家許可。

About Dr. Christopher Wheeler, Ph.D., President, StemVax, LLC

關於 StemVax, LLC 總裁克里斯托弗·惠勒博士

Dr. Wheeler has over 30 years of immunology and neurology research experience. His leadership experience is highlighted by his position and previous roles at Cedars-Sinai Medical Center Department of Neurosurgery. Dr. Wheeler was a Professor in the Department for over 20 years, and also served as The Operations Director of Vaccine Manufacturing Laboratory (1997-2018), as part of the Precision Medicine Initiative for Brain Tumors Department of Neurosurgery, and Glioma Immunotherapy Core Director (2003-2018).

惠勒博士擁有超過30年的免疫學和神經病學研究經驗。他在Cedars-Sinai醫學中心神經外科的職位和之前的職位突顯了他的領導經驗。惠勒博士在該系擔任教授超過20年,還曾擔任腦腫瘤精準醫療計劃神經外科系疫苗製造實驗室運營總監(1997-2018年)和膠質瘤免疫療法核心主任(2003-2018年)。

In 2023, Dr. Wheeler was appointed as a visiting scientist at UC Santa Cruz, Department of Chemistry & Biochemistry. The UC Santa Cruz Division of Physical & Biological Sciences is a world-leading public research institution with a reputation for instigating some of humanity's most high-impact discoveries and empowering students with immersive research experiences since 1965. It is part of the University of California, and maintains a mission to serve society through "transmitting advanced knowledge, discovering new knowledge, and functioning as an active working repository of organized knowledge" in the physical & biological sciences.

2023年,惠勒博士被任命爲加州大學聖克魯斯分校化學與生物化學系的訪問科學家。加州大學聖克魯斯分校物理與生物科學系是世界領先的公共研究機構,自1965年以來,它以發起一些人類最具影響力的發現和爲學生提供身臨其境的研究體驗而聞名。它是加利福尼亞大學的一部分,其使命是通過在物理和生物科學領域 “傳播先進知識,發現新知識並充當有組織知識的活躍工作庫” 來爲社會服務。

Dr. Wheeler's research has been highlighted by publications in numerous high-impact, paradigm shifting manuscripts and several patents. As part of his career achievements, he has executed scientific aspects of commercialization, validation, funding, and marketing for the development of Alzheimer's Disease (AD) biomarker technology. Dr Wheeler is a 2023 recipient of the prestigious Golden Axon Award presented at the World Brain Mapping Foundation (WBMF) Annual Congress.

惠勒博士的研究在衆多具有高影響力、改變範式的手稿和多項專利中得到了突出強調。作爲其職業成就的一部分,他曾爲阿爾茨海默氏病(AD)生物標誌物技術的開發執行過商業化、驗證、融資和營銷等科學方面的工作。惠勒博士是2023年在世界大腦映射基金會(WBMF)年會上頒發的久負盛名的金軸突獎的獲得者。

StemVax Therapeutics is a Translational Biotechnology Company that develops novel therapies for brain tumor patients. Research is focused on the development of immunotherapeutic approaches to treating patients with Glioblastoma, a devastating brain cancer. Additional research efforts are centered on novel drug development to target Cancer Stem cells and other multi-resistant cancer cells.

StemVax Therapeutics是一家轉化生物技術公司,爲腦腫瘤患者開發新療法。研究的重點是開發免疫治療方法來治療膠質母細胞瘤患者,這是一種毀滅性的腦癌。其他研究工作集中在靶向癌症幹細胞和其他多重耐藥癌細胞的新藥開發上。

StemVax became a wholly owned subsidiary of NovAccess Global, Inc. in October of 2020 to rapidly accelerate its portfolio through clinical trials and successfully bring safe and efficacious novel immunotherapeutics to market. Their mission is to make a difference in glioblastoma and other brain tumor patients' lives through novel immunotherapeutics.

StemVax於2020年10月成爲NovAccess Global, Inc.的全資子公司,旨在通過臨床試驗迅速加快其產品組合,併成功地將安全有效的新型免疫療法推向市場。他們的使命是通過新的免疫療法改變膠質母細胞瘤和其他腦腫瘤患者的生活。

About TLR-AD1

關於 TLR-AD1

TLR-AD1 is designed to activate anti-tumor immune responses against brain tumors using immune-activating dendritic cells combined with the patient's own tumor proteins. The resulting dendritic cell vaccines are matured with a proprietary combination of Toll-like receptor (TLR) adjuvants to boost their immune-activating potency beyond current vaccine preparations.

TLR-AD1 旨在使用免疫激活樹突狀細胞與患者自身腫瘤蛋白結合來激活針對腦腫瘤的抗腫瘤免疫反應。由此產生的樹突狀細胞疫苗使用專有的Toll樣受體(TLR)佐劑組合進行成熟,以增強其免疫激活效力,超越當前疫苗製劑。

The Company's therapeutic path involves a transformational process where tumor-killing immune responses for malignant glioma (MG) cells are higher than that of previous immunotherapies. This unique process involves the addition of proprietary substances to create a "cocktail" for more personalized treatment that substantially increases clinical benefits for patients.

該公司的治療路徑涉及一個變革過程,在該過程中,惡性神經膠質瘤(MG)細胞的腫瘤殺傷免疫反應高於先前的免疫療法。這種獨特的過程包括添加專有物質,製成 “混合物”,以實現更個性化的治療,從而顯著提高患者的臨床益處。

Glioblastoma is a form of aggressive brain cancer that annually impacts approximately 250,000 people globally and is on the rise in many countries, according to NovAccess scientists and published reports. The market data is more alarming, with glioblastoma accounting for approximately 50% of all malignant brain cancers diagnosed in the United States each year, and more than 10,000 Americans dying from this tumor type annually. Less than 5% of people with this cancer live longer than five years after their diagnosis. The global glioblastoma treatment market was estimated to be valued in excess of $2 billion in 2020, with projections for a compounded annual growth rate of more than 8% throughout the remainder of the decade.

根據NovAccess的科學家和已發表的報告,膠質母細胞瘤是一種侵襲性腦癌,每年影響全球約25萬人,並且在許多國家呈上升趨勢。市場數據更加令人震驚,膠質母細胞瘤約佔美國每年診斷出的所有惡性腦癌的50%,每年有超過10,000名美國人死於這種腫瘤類型。在患有這種癌症的人中,只有不到5%的患者在診斷後的壽命超過五年。據估計,到2020年,全球膠質母細胞瘤治療市場的價值將超過20億美元,預計在本十年的剩餘時間裏,複合年增長率將超過8%。

In 2022, the U.S. FDA granted Orphan Drug designation to TRL-AD1. NovAccess Global is preparing to submit an Investigational New Drug (IND) application to the FDA for TLR-AD1. In advance of the IND filing, the Company expects to announce a partnership with a clinical manufacturing organization for vaccine testing and production readiness for phase I-II clinical trials of TLR-AD1.

2022 年,美國食品藥品管理局授予 TRL-AD1 孤兒藥稱號。NovAccess Global正準備向美國食品藥品管理局提交 TLR-AD1 的研究性新藥(IND)申請。在提交IND申請之前,該公司預計將宣佈與一家臨床製造組織建立合作伙伴關係,爲疫苗測試和爲 TLR-AD1 的I-II期臨床試驗做好生產準備。

About NovAccess Global

關於 NovAccess

NovAccess Global is a biomedical company accelerating novel cancer diagnostics and therapeutics. Our goal is to discover, develop and bring to market novel and innovative medicine and medical devices to improve the quality of care for cancer and neurological patients.

NovAccess Global是一家加速新型癌症診斷和治療的生物醫學公司。我們的目標是發現、開發新穎和創新的藥物和醫療器械並將其推向市場,以提高癌症和神經系統患者的護理質量。

Follow us on social media and stay up to date on all of our developments:

在社交媒體上關注我們,隨時了解我們的所有最新動態:

Forward-Looking Statement

前瞻性陳述

This press release 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, and such forward-looking statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. "Forward-looking statements" describe future expectations, plans, results, or strategies and are generally preceded by words such as "may," "future," "plan" or "planned," "will" or "should," "expected," "anticipates," "draft," "eventually" or "projected." You are cautioned that such statements are subject to a multitude of risks and uncertainties that could cause future circumstances, events, or results to differ materially from those projected in the forward-looking statements, including the risks that actual results may differ materially from those projected in the forward-looking statements as a result of various factors, and other risks identified in the Company's disclosures or filings with the Securities Exchange Commission. Additional investments by Sumner Global are subject to various contingencies, including Sumner obtaining the funding required to make the additional investments, and may not occur when expected or at all. You are further cautioned that penny stocks and stocks of smaller companies like NovAccess Global Inc. are inherently volatile and risky and that no investor should buy this stock unless they can afford the loss of their entire investment. The Company disclaims any obligation to update any forward-looking statements to reflect events or circumstances after the date thereof.

本新聞稿包含經修訂的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”,此類前瞻性陳述是根據1995年《私人證券訴訟改革法》的安全港條款作出的。“前瞻性陳述” 描述未來的預期、計劃、結果或策略,前面通常以 “可能”、“未來”、“計劃” 或 “計劃”、“將” 或 “應該”、“預期”、“預期”、“草稿”、“最終” 或 “預測” 等詞語開頭。請注意,此類陳述存在多種風險和不確定性,可能導致未來的情況、事件或結果與前瞻性陳述中的預測存在重大差異,包括由於各種因素,實際業績可能與前瞻性陳述中的預測存在重大差異的風險,以及公司向證券交易委員會披露或文件中確定的其他風險。Sumner Global的額外投資受各種突發事件的影響,包括薩姆納獲得進行額外投資所需的資金,可能不會按預期進行或根本不會發生。進一步提醒您,細價股和像NovAccess Global Inc.這樣的小型公司的股票本質上是波動性和風險性的,除非投資者能夠承受全部投資的損失,否則任何投資者都不應購買該股票。公司不承擔任何更新任何前瞻性陳述以反映其後的事件或情況的義務。

Investor Relations Contact:

投資者關係聯繫人:

Jordan Darrow
Darrow Associates
631-766-4528
jdarrow@darrowir.com

喬丹·達羅
達羅合夥人
631-766-4528
jdarrow@darrowir.com

SOURCE: NovAccess Global Inc.

來源:NovAccess 全球公司


譯文內容由第三人軟體翻譯。


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