share_log

Marvel Biosciences Shares Positive Results of MB204 in the Oprm1 Model of Autism

Marvel Biosciences Shares Positive Results of MB204 in the Oprm1 Model of Autism

Marvel生物科學公司宣佈MB204在自閉症Oprm1模型中取得積極結果
newsfile ·  10/10 21:00

Calgary, Alberta--(Newsfile Corp. - October 10, 2024) - Marvel Biosciences Corp. (TSXV: MRVL) (OTCQB: MBCOF), and its wholly owned subsidiary, Marvel Biotechnology Inc. (collectively the "Company" or "Marvel"), today shared promising results from a recent study on MB204. The research was conducted by Drs. Julie Le Merrer and Jerome Becker of the iBraiN Institute in Tours, France, to investigate the impact of MB204 in the Oprm1 mouse model of autism (widely used to study social behavior deficits). Marvel is pleased to report that just one hour after administering a single oral dose of MB204, the drug successfully reversed the social behaviour deficits typically seen in the model.

加拿大艾伯塔省卡爾加里-(Newsfile corp.-2024年10月10日)-奇蹟生物科技公司(tsxv: MRVL)(otcqb: MBCOF)及其全資子公司Marvel生物技術公司(統稱「公司」或「Marvel」),今天分享了最新研究MB204的可喜成果。這項研究由法國圖爾市iBraiN研究所的朱莉·勒梅爾博士和傑羅姆·貝克博士進行,旨在調查MB204在自閉症(廣泛用於研究社交行爲缺陷)的Oprm1小鼠模型中的影響。Marvel很高興地報告,在單次口服MB204後僅一個小時,該藥成功逆轉了該模型中通常出現的社交行爲缺陷。

Key Highlights:

亮點: 1.肺炎的全球發病率估計在每1000人年之間變化1.5至14例之間。 2.肺炎的患病率最高爲小兒人群(6.8%),其次爲老年人群(3.75%),在非大都市城市(人口在100萬以下)中最顯著。 3.美國的肺炎年發病率爲每10000名成年人24.8例。 4.在需要住院的重症肺炎患者中,報告的死亡率爲4%至37%,並隨着年齡的增長而上升。 5.肺炎是全球兒童死亡的最常見感染性死因。根據世衛組織的數據,該疾病造成5歲以下兒童死亡總數的14%。

  • A high dose of MB204 (2.5 mg/kg) significantly restored social behaviour in all measured endpoints (p<0.0001). Improvements were seen in social interaction behaviours including, the number and duration of nose contacts, the number and duration of paw contacts, and time spent self-grooming, amongst others.
  • A lower dose of MB204 (1 mg/kg) also reversed nearly all social behaviour deficits, showing a clear connection between dose and response.
  • The higher dose of MB204 not only improved/restored social interactions in Oprm1 (autistic) mice, but even outperformed the social interactions of normal (non-autistic) mice on several endpoints, demonstrating MB204's potent pro-social effect.
  • MB204高劑量(2.5 mg/kg)顯著恢復了所有測定終點的社交行爲(p
  • MB204低劑量(1 mg/kg)也逆轉了幾乎所有社交行爲缺陷,顯示了劑量與反應之間的明顯關聯。
  • MB204更高劑量不僅改善/恢復了Oprm1(自閉症)小鼠的社交互動,甚至在幾個終點上超越了正常(非自閉症)小鼠的社交互動,展示了MB204強有力的親社會效應。

"These results are very encouraging," said Drs. Le Merrer and Becker, "MB204, at both doses, nearly reversed all the social deficits/endpoints in our autism model, and in some cases, the Oprm1 animals appeared to be more sociable than normal animals. We have previously tested Istradefylline (an off-patent approved drug similar to MB204), in multiple models of autism such as Oprm1, Mecp2, and Fmr1 but we have not seen this level of improvement or the hyper-social effect before."

「這些結果非常令人鼓舞,」勒梅爾博士和貝克博士表示,「MB204在兩種劑量下幾乎逆轉了我們自閉症模型中的所有社交缺陷/終點,有些情況下,Oprm1動物的社交行爲似乎比正常動物更合群。我們之前已在多個自閉症模型(如 Oprm1、Mecp2 和 Fmr1)中測試過伊斯特拉德非林(一種與MB204類似的已獲批准的非專利藥物),但之前從未見過這種改善水平或超社交效應。」

Currently, Drs. Le Merrer and Becker are now testing MB204 in another chronic Rett syndrome model (Mecp2) and are looking forward to seeing how it performs 'head-to-head' against the approved drug Trofinetide.

目前,勒梅爾博士和貝克博士正在另一個慢性雷特氏綜合徵模型(Mecp2)中測試MB204,並期待看到它如何與已批准的藥物Trofinetide 進行「硬碰硬」的比較。

"We are very pleased with these findings for MB204 and intend to publish them in a peer reviewed journal," said Marvel's Chief Science Officer, Dr. Mark Williams. "MB204 is currently being tested in two very clinically relevant autism spectrum disorder models of Rett syndrome (Mecp2) and Fragile X syndrome (Fmr1), the latter is in collaboration with the Fraxa Research Foundation, and we look forward to reviewing the results."

「我們對MB204的這些發現感到非常高興,並計劃在同行評審的期刊上發表,」 Marvel的首席科學官,Mark Williams博士說。「MB204目前正在兩種與臨床相關的自閉症譜系障礙模型中進行測試,包括雷特綜合徵(Mecp2)和脆性X綜合徵(Fmr1),後者是與Fraxa研究基金會合作的,我們期待審查結果。」

About Marvel Biosciences Corp.

關於奇妙生物科技公司:

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公司及其全資子公司Marvel生物技術公司是加拿大卡爾加里一家臨床前階段的藥品開發生物技術公司,利用"藥品重新開發"方法進行藥物開發。歷史上,當一種新的藥物類別被開發出來時,它被優化爲特定的作用靶標,但通常只被批准用於特定的疾病。通常,會發現涉及相同作用靶標的新疾病,但原始批准的藥物可能由於專利剩餘存續期不足,不足以對新的疾病適用。Marvel爲新的疾病適應研究和開發原批准藥物的新合成化學衍生物。由公司開發的新潛在資產,我們將會尋求專利保護。該公司認爲這種商業模式與傳統生物技術公司相比,能夠更少風險、成本和時間地開發其資產。

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.目前已經開發出幾種新化學實體,使用已知的過期藥物的合成化學衍生物來抑制A2a腺苷受體,適用於神經系統疾病(抑鬱症和焦慮症、阿爾茨海默病、ADHD)、癌症和非酒精性脂肪肝等非神經系統疾病。Marvel還在探索其他未公開的目標,以擴大其資產流水線。

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

Marvel Biosciences Corp.
J. Roderick(Rod) Matheson,首席執行官。
馬克·威廉姆斯博士,總裁和首席科學官
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.

無論是TSX Venture交易所還是其監管服務提供商(如TSXV政策中所定義的那樣),都不對本新聞稿的充分性或準確性負責。

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.

本新聞發佈中所有有關公司及其子公司(統稱「各方」)的信息均由Marvel分別提供,供本新聞發佈納入,並且各自的董事和高管人員都僅就有關方面相互依賴獲得了信息。

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.

本新聞發佈可能包含前瞻性聲明和其他陳述,而不是歷史事實。前瞻性聲明通常用諸如「將」、「可能」、「應該」、「預期」和類似表達方式來識別。本發佈中包含的所有陳述,除歷史事實陳述外,包括但不限於有關公司未來計劃和目標的陳述,都是有風險和不確定性的前瞻性聲明。不保證這類聲明會證明是準確的,實際結果和未來事件可能會與這類聲明所預期的有所不同。可能導致實際結果與公司預期不同的重要因素包括本新聞發佈所述各方的風險以及其他風險和不確定性,其許多情況超出公司的控制範圍。因此,公司不能保證上述事件將按照此處或全部披露的條款發生,也不能保證時間的履行。本新聞發佈中包含的前瞻性聲明明確受到此警告聲明的約束。本新聞發佈中包含的前瞻性聲明是截至本新聞發佈日期所述的,公司將根據加拿大證券法的規定明確更新或修訂包含在其中的任何前瞻性聲明。

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。
    搶先評論