share_log

Zentek Announces Promising Preclinical Safety and Toxicity Results Achieved by Triera Biosciences Ltd. for C19HBA

Zentek Announces Promising Preclinical Safety and Toxicity Results Achieved by Triera Biosciences Ltd. for C19HBA

Zentek 宣佈 Triera Biosciences Ltd. 在 C19HBA 方面取得的令人鼓舞的臨床前安全性和毒性結果
Accesswire ·  03/25 08:00

GUELPH, ON / ACCESSWIRE / March 25, 2024 / Zentek Ltd. ("Zentek" or the "Company") (Nasdaq:ZTEK)(TSX-V:ZEN), announces that its wholly-owned subsidiary Triera Biosciences Ltd. ("Triera") has completed testing demonstrating that its C19HBA SARS-CoV-2 universal aptamer built on the proprietary high-binding affinity aptamer platform has shown a promising safety and toxicity profile in preclinical testing. This is a critical step in the path towards the development of a human therapeutic.

安大略省蓋爾夫/ACCESSWIRE/2024年3月25日/Zentek Ltd.(“Zentek” 或 “公司”)(納斯達克股票代碼:ZTEK)(多倫多證券交易所股票代碼:ZEN)宣佈,其全資子公司Triera Biosciences Ltd.(“Triera”)(“Triera”)已完成測試,表明其建立在專有的高結合親和力適配體平台上的 C19HBA SARS-CoV-2 通用適配體顯示出前景看好臨床前測試中的安全性和毒性概況。這是人類療法開發道路上的關鍵一步。

Previously, the Company reported successful efficacy when C19HBA was tested as a prophylaxis and as a therapeutic. In repeated trials against SARS-CoV-2 variants, C19HBA has matched or exceeded the clinical protection compared to a leading monoclonal antibody (LMA).

此前,該公司報告說,當 C19HBA 作爲預防和治療進行測試時,取得了成功的療效。在針對 SARS-CoV-2 變體的反覆試驗中,與領先的單克隆抗體 (LMA) 相比,C19HBA 已達到或超過臨床保護水平。

In a trial completed in February 2024 by the Miller lab at McMaster University, the safety and toxicity of C19HBA was assessed through a study that administered 258 μM of C19HBA intranasally to one cohort of mice with a similar-sized cohort receiving sham treatment. After two hours, half the mice from each cohort were sacrificed while the remaining mice were infected with a lethal challenge of the ancestral variant of SARS-CoV-2. After 24 hours all infected mice were sacrificed, and serum and BAL fluid samples were collected. These samples were analyzed for inflammatory cell infiltration and full cytokine panel.

在麥克馬斯特大學米勒實驗室於 2024 年 2 月完成的一項試驗中,通過一項研究評估了 C19HBA 的安全性和毒性,該研究對一組接受虛假治療的小鼠進行了鼻內注射 258 μM 的 C19HBA。兩小時後,每個隊列中有一半的小鼠被犧牲,而其餘的小鼠則感染了SARS-CoV-2祖先變種的致命挑戰。24 小時後,犧牲了所有受感染的小鼠,並採集了血清和 BAL 液體樣本。對這些樣本進行了炎性細胞浸潤和完整的細胞因子試劑盒分析。

The inflammatory cell infiltration study demonstrated that mice treated with C19HBA had similar levels of macrophages, neutrophils, and monocytes as the naïve mice both at the two-hour mark after C19HBA administration and 24 hours after infection.

炎症細胞浸潤研究表明,無論是在給藥 C19HBA 後的兩小時內還是在感染後 24 小時,接受 C19HBA 治療的小鼠的巨噬細胞、中性粒細胞和單核細胞水平都與天真小鼠相似。

The cytokine panel analyzed 44 different biomarkers from the Bronchoalveolar Lavage ("BAL")

細胞因子小組分析了來自支氣管肺泡灌洗液(“BAL”)的44種不同的生物標誌物

BAL fluid of sacrificed mice. The major cytokine markers, VEGF-A and TNFα were consistent between naïve mice and those treated with C19HBA.

被犧牲小鼠的 BAL 液體。幼鼠和接受 C19HBA 治療的小鼠之間的主要細胞因子標誌物 VEGF-A 和 TNFα 是一致的。

In reviewing both reports, Dr. Miller concluded that, "C19HBA appears to be safe and well-tolerated in mice both before and after SARS-CoV-2 infection. Importantly, the therapeutic did not exacerbate the induction of any unexpected inflammatory cytokines or chemokines in the airways of treated mice, nor did they elicit any pathological recruitment of inflammatory innate immune cells."

在審查這兩份報告時,米勒博士得出結論:“無論是在感染SARS-CoV-2之前還是之後,C19HBA 在小鼠身上似乎都是安全且耐受性良好的。重要的是,該療法沒有加劇接受治療的小鼠氣道中任何意想不到的炎症細胞因子或趨化因子的誘導,也沒有引起炎症性先天免疫細胞的任何病理招募。”

"As we presented our results of C19HBA a main concern raised was whether the therapeutic/prophylactic was safe to use. Although further work is required, this data supports that our aptamer platform is safe and works in a manner that we expected. These results give us confidence as we continue to expand our pipeline into other infectious diseases like influenza and into the oncology space." said Greg Fenton, CEO of the Company and Triera. "When we find aptamers with therapeutic potential, we have a greater certainty from this study that the aptamers will be safe for human use."

“當我們介紹 C19HBA 的結果時,提出的主要問題是該療法/預防藥物的使用是否安全。儘管需要做進一步的工作,但這些數據支持我們的aptamer平台是安全的,並且可以按我們預期的方式運行。這些結果使我們有信心繼續將產品線擴展到流感等其他傳染病和腫瘤學領域。” 該公司和Triera首席執行官格雷格·芬頓說。“當我們發現具有治療潛力的適配體時,我們從這項研究中可以更確定這些適配體可以安全地供人使用。”

About Triera Biosciences Ltd.

關於特瑞拉生物科學有限公司

Triera holds an exclusive, worldwide royalty bearing license from McMaster University to use and practice all aptamer and DNAyme uses developed by McMaster University for the next 20 years. Triera and McMaster's combined expertise and capabilities in aptamer technology offer significant potential to reduce the cost and time required for the development of new treatments.

Triera擁有麥克馬斯特大學頒發的全球獨家特許權使用費許可,可以在未來20年內使用和實踐麥克馬斯特大學開發的所有適配體和DNayMe用途。Triera和McMaster在適配體技術方面的綜合專業知識和能力爲降低開發新療法所需的成本和時間提供了巨大的潛力。

About Zentek Ltd.

關於 Zentek Ltd

Zentek is an ISO 13485:2016 certified intellectual property technology company focused on the research, development and commercialization of novel products seeking to give the Company's commercial partners a competitive advantage by making their products better, safer, and greener.

Zentek是一家通過ISO 13485:2016 認證的知識產權技術公司,專注於新產品的研究、開發和商業化,旨在通過使公司的商業合作伙伴的產品更好、更安全、更環保,從而爲其商業合作伙伴提供競爭優勢。

Zentek's patented technology platform ZenGUARD, is shown to have 99-per-cent anti-microbial activity and to significantly increase the bacterial and viral filtration efficiency of both surgical masks and HVAC (heating, ventilation, and air conditioning) systems. Zentek's ZenGUARD production facility is located in Guelph, Ontario.

Zentek的專利技術平台ZenGuard被證明具有99%的抗菌活性,可顯著提高外科口罩和HVAC(採暖、通風和空調)系統的細菌和病毒過濾效率。Zentek 的 ZenGuard 生產設施位於安大略省圭爾夫。

Zentek, through its wholly-owned subsidiary Triera Biosciences Ltd., has a global exclusive license to the aptamer-based platform technology developed by McMaster University, which is being jointly developed by Zentek and McMaster for both the diagnostic and therapeutic markets.

Zentek通過其全資子公司Triera Biosciences Ltd. 獲得了麥克馬斯特大學開發的基於適配器的平台技術的全球獨家許可,該技術由Zentek和McMaster共同開發,用於診斷和治療市場。

The Company is not making any express or implied claims that its aptamer technology has the ability to eliminate, cure or contain the COVID-19 (or SARS-CoV-2 Coronavirus) at this time.

該公司目前沒有明示或暗示地聲稱其適配體技術有能力消除、治癒或遏制 COVID-19(或SARS-CoV-2冠狀病毒)。

For further information contact:

欲了解更多信息,請聯繫:

Dr. Colin Van der Kuur, Chief Science Officer
Email: cvanderkuur@triera.ca

首席科學官 Colin Van der Kuur 博士
電子郵件:cvanderkuur@triera.ca

To find out more about Zentek, please visit our website at . A copy of this news release and all material documents in respect of the Company may be obtained on Zentek's SEDAR+ profile at

要了解有關 Zentek 的更多信息,請訪問我們的網站。本新聞稿和與公司有關的所有重要文件的副本可在Zentek的SEDAR+個人資料上獲得,網址爲

Forward-Looking Statements

前瞻性陳述

This news release contains forward-looking statements. Since forward-looking statements address future events and conditions, by their very nature they involve inherent risks and uncertainties. Although Zentek believes that the assumptions and factors used in preparing the forward-looking information in this news release are reasonable, undue reliance should not be placed on such information, which only applies as of the date of this news release, and no assurance can be given that such events will occur in the disclosed time frames or at all. Zentek disclaims any intention or obligation to update or revise any forward-looking information, whether as a result of new information, future events or otherwise, other than as required by law.

本新聞稿包含前瞻性陳述。由於前瞻性陳述涉及未來的事件和狀況,因此就其本質而言,它們涉及固有的風險和不確定性。儘管Zentek認爲在本新聞稿中準備前瞻性信息時使用的假設和因素是合理的,但不應過分依賴此類信息,此類信息僅在本新聞稿發佈之日適用,也無法保證此類事件會在披露的時間範圍內發生或根本不會發生。除非法律要求,否則Zentek不打算或有義務更新或修改任何前瞻性信息,無論是由於新信息、未來事件還是其他原因。

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

多倫多證券交易所風險投資交易所及其監管服務提供商(該術語在多倫多證券交易所風險投資交易所的政策中定義)均不對本新聞稿的充分性或準確性承擔責任。

SOURCE: Zentek Ltd.

來源:Zentek Ltd.


声明:本內容僅用作提供資訊及教育之目的,不構成對任何特定投資或投資策略的推薦或認可。 更多信息
    搶先評論