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Marvel Biosciences to Collaborate With Tau Expert Dr. Emmanuel Planel

Marvel Biosciences to Collaborate With Tau Expert Dr. Emmanuel Planel

漫威生物科學將與 Tau 專家 Emmanuel Planel 博士合作
newsfile ·  01/09 05:30

Calgary, Alberta--(Newsfile Corp. - January 8, 2024) - Marvel Biosciences Corp. (TSXV: MRVL) (OTCQB: MBCOF) and its wholly owned subsidiary, Marvel Biotechnology Inc. (collectively the "Company" or "Marvel"), is pleased to announce a collaboration with Professor Emmanuel Planel of Laval University to study the acute effect of MB-204 on Tau protein phosphorylation in mice. Abnormal tau phosphorylation is a hallmark of neurodegenerative diseases such as Alzheimer's disease.

艾伯塔省卡爾加里--(Newsfile Corp.-2024 年 1 月 8 日)- 漫威生物科學公司(多倫多證券交易所股票代碼:MRVL)(OTCQB:MBCOF) 及其全資子公司漫威生物技術公司(統稱”公司“或”奇蹟“),很高興地宣佈與拉瓦爾大學的伊曼紐爾·普拉內爾教授合作,研究 MB-204 對小鼠體內 Tau 蛋白磷酸化的急性影響。異常 tau 磷酸化是阿爾茨海默氏病等神經退行性疾病的標誌。

"We are very pleased to have the opportunity to collaborate with Dr. Planel, a world leader on Tau pathogenesis," commented Dr. Mark Williams, CSO of Marvel. "The A2a receptor, the target of MB-204, has repeatedly been shown to modulate Tau phosphorylation in multiple disease models. When Tau is hyperphosphorylated, it becomes more prone to clumping, similar to beta amyloid. We intend to test the effect of MB-204 on rapidly reducing Tau phosphorylation in mice using a simple technique pioneered by Dr. Planel."

漫威首席安全官馬克·威廉姆斯博士評論說:“我們很高興有機會與Tau發病機制領域的全球領導者普萊內爾博士合作。”“A2a 受體是 MB-204 的靶點,在多種疾病模型中反覆被證明可以調節 Tau 磷酸化。當 Tau 過度磷酸化時,它變得更容易結塊,類似於 β 澱粉樣蛋白。我們打算使用普萊內爾博士首創的一種簡單技術測試 MB-204 對快速降低小鼠體內 Tau 磷酸化的影響。”

"I am pleased to be working with Marvel on testing their A2a antagonist in our acute mouse model of Tau hyperphosphorylation," noted Dr. Planel. "The pathways affected by the A2a receptor seem to be a very reasonable approach to reducing Tau phosphorylation and we look forward to testing MB-204 in our model."

普萊內爾博士指出:“我很高興能與漫威合作,在我們的Tau過度磷酸化急性小鼠模型中測試他們的A2a拮抗劑。”“受A2a受體影響的路徑似乎是減少Tau磷酸化的非常合理的方法,我們期待在我們的模型中測試 MB-204。”

"With the approvals of beta amyloid targeted treatments such as lecanemab and aducanumab for Alzheimer's Disease, more attention is turning to Tau," said Rod Matheson, CEO of Marvel. "MB-204 has completed its pre-clinical 4-week GLP toxicology studies and cGMP manufacturing and is Phase 1 clinical trial ready. We will continue to update the market on our progress with our pre-clinical and clinical programs."

漫威首席執行官羅德·馬西森說:“隨着用於阿爾茨海默氏病的lecanemab和aducanumab等β澱粉樣蛋白靶向療法的批准,越來越多的注意力轉向了Tau。”“MB-204 已經完成了爲期 4 周的臨床前 GLP 毒理學研究和 cGMP 製造,並已準備就緒 1 期臨床試驗。我們將繼續向市場介紹我們的臨床前和臨床項目的最新進展。”

MB-204 is a novel fluorinated derivative of the U.S. FDA-approved adenosine A2a receptor antagonist, Istradefylline which has completed cGMP manufacturing and 4-week GLP toxicology studies.

MB-204 是美國食品藥品管理局批准的腺苷 a2a 受體拮抗劑 Istradefylline 的新型氟化衍生物,該藥物已完成 cGMP 的生產和爲期 4 周的 GLP 毒理學研究。

About Marvel Biosciences Corp.

關於漫威生物科學公司

Marvel Biosciences Corp., and its wholly owned subsidiary, Marvel Biotechnology Inc., is a Calgary-based pre-clinical stage pharmaceutical development biotechnology company that utilizes a "drug redevelopment" approach to drug development. Historically, when a new class of drug is developed, it is optimized for a particular target, but typically only approved for a specific disease. Often, a new disease is identified which involves the same target, however, pending the remaining patent life, the originally approved drug may not have sufficient time left for it to be commercially viable to be developed for the new disease indication. Marvel develops new synthetic chemical derivatives of the original approved drug for the new disease indication. Patent protection is sought, as the new potential asset is developed by the Company. The Company believes the business model results in significantly less risk, cost and time to develop its assets compared to traditional biotechnology companies.

Marvel Biosciences Corp. 及其全資子公司Marvel Biotechnology Inc. 是一家總部位於卡爾加里的臨床前階段藥物開發生物技術公司,採用 “藥物重建” 方法進行藥物開發。歷史上,當開發一類新藥物時,它會針對特定的靶標進行優化,但通常僅批准用於特定疾病。通常會發現一種涉及相同靶標的新疾病,但是,在剩餘的專利期限之前,最初批准的藥物可能沒有足夠的時間來開發針對新疾病適應症的商業可行性。Marvel 開發了用於新疾病適應症的原始批准藥物的新合成化學衍生物。隨着公司開發新的潛在資產,正在尋求專利保護。該公司認爲,與傳統的生物技術公司相比,這種商業模式可以顯著減少開發資產的風險、成本和時間。

Marvel Biotechnology Inc. has currently developed several new chemical entities, using synthetic chemical derivatives of known, off-patent drugs, that inhibit the A2a adenosine receptor with application to neurological diseases (depression & anxiety, Alzheimer's, Autism and ADHD), and the non-neurological conditions of cancer and non-alcoholic steatohepatitis. Marvel is also exploring additional undisclosed targets to expand its asset pipeline.

Marvel Biotechnology Inc.目前已開發了幾種新的化學實體,使用已知的非專利藥物的合成化學衍生物,這些藥物可抑制A2a腺苷受體,應用於神經系統疾病(抑鬱和焦慮症、阿爾茨海默氏症、自閉症和注意力缺陷多動障礙),以及癌症和非酒精性脂肪肝炎等非神經系統疾病。漫威還在探索其他未公開的目標,以擴大其資產管道。

Contact Information

聯繫信息

Marvel Biosciences Corp.
J. Roderick (Rod) Matheson, Chief Executive Officer or
Dr. Mark Williams, President and Chief Science Officer
Tel: 403 770 2469

漫威生物科學公司
J. Roderick (Rod) Matheson,首席執行官或
總裁兼首席科學官馬克·威廉姆斯博士
電話:403 770 2469

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

多倫多證券交易所風險交易所及其監管服務提供商(該術語在多倫多證券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。

All information contained in this news release with respect to the Company and its subsidiary, (collectively, the "Parties") were supplied by Marvel, respectively, for inclusion herein and each parties' directors and officers have relied on each other for any information concerning such Party.

本新聞稿中包含的與公司及其子公司(統稱 “雙方”)有關的所有信息均由漫威分別提供,以供納入此處,雙方的董事和高級管理人員相互依賴以獲取有關該方的任何信息。

This news release may contain forward-looking statements and other statements that are not historical facts. Forward-looking statements are often identified by terms such as "will", "may", "should", "anticipate", "expects" and similar expressions. All statements other than statements of historical fact, included in this release, including, without limitation, statements regarding the future plans and objectives of the Company are forward-looking statements that involve risks and uncertainties. There can be no assurance that such statements will prove to be accurate and actual results and future events could differ materially from those anticipated in such statements. Important factors that could cause actual results to differ materially from the expectations of the Company and include other risks detailed from time to time in the filings made by the Company under securities regulations.

本新聞稿可能包含前瞻性陳述和其他非歷史事實的陳述。前瞻性陳述通常用 “將”、“可能”、“應該”、“預期”、“期望” 等術語和類似表述來識別。除歷史事實陳述外,本新聞稿中包含的所有陳述,包括但不限於有關公司未來計劃和目標的陳述,均爲涉及風險和不確定性的前瞻性陳述。無法保證此類陳述會被證明是準確的,實際結果和未來事件可能與此類聲明中的預期有重大差異。可能導致實際業績與公司預期存在重大差異的重要因素,包括公司根據證券監管提交的文件中不時詳述的其他風險。

To view the source version of this press release, please visit

要查看本新聞稿的源版本,請訪問

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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