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Marvel Biosciences Announces Testing MB-204 on Autism by French University

Marvel Biosciences Announces Testing MB-204 on Autism by French University

漫威生物科學宣佈由法國大學對自閉症進行 MB-204 測試
newsfile ·  02/21 05:30

Calgary, Alberta--(Newsfile Corp. - February 20, 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 it has begun testing MB-204 in the Oprm1 mouse model of autism in collaboration with Dr. Julie Le Merrer and Dr. Jerome Becker at the iBrain Institute, Tours, France.

艾伯塔省卡爾加里--(Newsfile Corp.-2024 年 2 月 20 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,它已開始與法國圖爾iBrain研究所的朱莉·勒默爾博士和傑羅姆·貝克爾博士合作,在Oprm1自閉症小鼠模型中測試 MB-204。

"We are going to test the effect of acute dosing of MB-204 in one of the prototypic models of autism, the Oprm1 mouse, looking specifically at sociability and stereotypic behaviour in the Y-maze model after acute dosing", said Dr. Mark Williams, CSO of Marvel. "We have seen immediate effects of MB-204 after a single dose in mouse models of depression, which gives us confidence the drug could offer improvements in these autistic behaviours after a short course of therapy."

漫威首席安全官馬克·威廉姆斯博士說:“我們將在自閉症的原型模型之一 Oprm1 小鼠中測試急性給藥 MB-204 的影響,專門研究 Y 迷宮模型在急性給藥後的社交能力和陳規定型行爲。”“我們在抑鬱症小鼠模型中看到了 MB-204 在小鼠抑鬱症模型中的立竿見影的效果,這使我們有信心在短期治療後該藥物可以改善這些自閉症行爲。”

"Autism is a very underserved medical condition that affects approximately 1 in 36 children", said Mr. Rod Matheson, CEO of Marvel, "and the social impact cost of autism in the US is expected to exceed $450B by 2025. There is an approved drug Daybue for Rett's Syndrome as of 2023, a very specific form of autism that affects about 1 in 10,000 girls. Based on the pre-clinical evidence we believe MB-204 could treat multiple forms of autism including Rett's Syndrome. Pending positive data, we intend to approach many of the autism foundations and venture philanthropy groups to support the testing MB-204 in other models of autism including Rett's Syndrome".

漫威首席執行官羅德·馬西森說:“自閉症是一種嚴重得不到充分治療的疾病,大約每36名兒童中就有1人受到影響,到2025年,美國自閉症的社會影響成本預計將超過4500億美元。截至2023年,有一種經批准的治療雷特氏綜合症的藥物Daybue,這是一種非常特殊的自閉症,大約每10,000名女孩中就有1人受到影響。根據臨床前證據,我們認爲 MB-204 可以治療多種形式的自閉症,包括雷特氏綜合症。在獲得積極數據之前,我們打算與許多自閉症基金會和風險慈善團體接觸,以支持在包括雷特氏綜合症在內的其他自閉症模型中測試 MB-204”。

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, 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、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。

The reader is cautioned that assumptions used in the preparation of any forward-looking information may prove to be incorrect. Events or circumstances may cause actual results to differ materially from those predicted, as a result of numerous known and unknown risks, uncertainties, and other factors, many of which are beyond the control of the Company. As a result, the Company cannot guarantee that the above events on the terms will occur and within the time disclosed herein or at all. The reader is cautioned not to place undue reliance on any forward-looking information. Such information, although considered reasonable by management at the time of preparation, may prove to be incorrect and actual results may differ materially from those anticipated. Forward-looking statements contained in this news release are expressly qualified by this cautionary statement. The forward-looking statements contained in this news release are made as of the date of this news release and the Company will update or revise publicly any of the included forward-looking statements as expressly required by Canadian securities law.

提醒讀者,在準備任何前瞻性信息時使用的假設都可能被證明是不正確的。由於許多已知和未知的風險、不確定性和其他因素,其中許多是公司無法控制的,事件或情況可能導致實際業績與預測存在重大差異。因此,本公司無法保證上述條款所述事件將在本文披露的時間內發生,也無法保證根本無法保證。提醒讀者不要過分依賴任何前瞻性信息。儘管管理層在編制時認爲此類信息是合理的,但可能被證明是不正確的,實際結果可能與預期的結果存在重大差異。本新聞稿中包含的前瞻性陳述受本警示聲明的明確限制。本新聞稿中包含的前瞻性陳述自本新聞發佈之日起作出,公司將按照加拿大證券法的明確要求公開更新或修改所包含的任何前瞻性陳述。

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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