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
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.
加拿大艾伯塔省卡尔加里-(Newsfile corp.-2024年10月10日)-奇迹生物科技公司(tsxv: MRVL)(otcqb: MBCOF)及其全资子公司Marvel生物技术公司(统称“公司”或“Marvel”),今天分享了最新研究MB204的可喜成果。这项研究由法国图尔市iBraiN研究所的朱莉·勒梅尔博士和杰罗姆·贝克博士进行,旨在调查MB204在自闭症(广泛用于研究社交行为缺陷)的Oprm1小鼠模型中的影响。Marvel很高兴地报告,在单次口服MB204后仅一个小时,该药成功逆转了该模型中通常出现的社交行为缺陷。
Key Highlights:
亮点: 1.肺炎的全球发病率估计在每1000人年之间变化1.5至14例之间。 2.肺炎的患病率最高为小儿人群(6.8%),其次为老年人群(3.75%),在非大都市城市(人口在100万以下)中最显著。 3.美国的肺炎年发病率为每10000名成年人24.8例。 4.在需要住院的重症肺炎患者中,报告的死亡率为4%至37%,并随着年龄的增长而上升。 5.肺炎是全球儿童死亡的最常见感染性死因。根据世卫组织的数据,该疾病造成5岁以下儿童死亡总数的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高剂量(2.5 mg/kg)显著恢复了所有测定终点的社交行为(p
- MB204低剂量(1 mg/kg)也逆转了几乎所有社交行为缺陷,显示了剂量与反应之间的明显关联。
- MB204更高剂量不仅改善/恢复了Oprm1(自闭症)小鼠的社交互动,甚至在几个终点上超越了正常(非自闭症)小鼠的社交互动,展示了MB204强有力的亲社会效应。
"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."
“这些结果非常令人鼓舞,”勒梅尔博士和贝克博士表示,“MB204在两种剂量下几乎逆转了我们自闭症模型中的所有社交缺陷/终点,有些情况下,Oprm1动物的社交行为似乎比正常动物更合群。我们之前已在多个自闭症模型(如 Oprm1、Mecp2 和 Fmr1)中测试过伊斯特拉德非林(一种与MB204类似的已获批准的非专利药物),但之前从未见过这种改善水平或超社交效应。”
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,勒梅尔博士和贝克博士正在另一个慢性雷特氏综合征模型(Mecp2)中测试MB204,并期待看到它如何与已批准的药物Trofinetide 进行“硬碰硬”的比较。
"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."
“我们对MB204的这些发现感到非常高兴,并计划在同行评审的期刊上发表,” Marvel的首席科学官,Mark Williams博士说。“MB204目前正在两种与临床相关的自闭症谱系障碍模型中进行测试,包括雷特综合征(Mecp2)和脆性X综合征(Fmr1),后者是与Fraxa研究基金会合作的,我们期待审查结果。”
About Marvel Biosciences Corp.
关于奇妙生物科技公司:
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公司及其全资子公司Marvel生物技术公司是加拿大卡尔加里一家临床前阶段的药品开发生物技术公司,利用"药品重新开发"方法进行药物开发。历史上,当一种新的药物类别被开发出来时,它被优化为特定的作用靶标,但通常只被批准用于特定的疾病。通常,会发现涉及相同作用靶标的新疾病,但原始批准的药物可能由于专利剩余存续期不足,不足以对新的疾病适用。Marvel为新的疾病适应研究和开发原批准药物的新合成化学衍生物。由公司开发的新潜在资产,我们将会寻求专利保护。该公司认为这种商业模式与传统生物技术公司相比,能够更少风险、成本和时间地开发其资产。
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.目前已经开发出几种新化学实体,使用已知的过期药物的合成化学衍生物来抑制A2a腺苷受体,适用于神经系统疾病(抑郁症和焦虑症、阿尔茨海默病、ADHD)、癌症和非酒精性脂肪肝等非神经系统疾病。Marvel还在探索其他未公开的目标,以扩大其资产流水线。
Contact Information
联系信息
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,首席执行官。
马克·威廉姆斯博士,总裁和首席科学官
电话: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.
无论是TSX Venture交易所还是其监管服务提供商(如TSXV政策中所定义的那样),都不对本新闻稿的充分性或准确性负责。
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.
本新闻发布中所有有关公司及其子公司(统称“各方”)的信息均由Marvel分别提供,供本新闻发布纳入,并且各自的董事和高管人员都仅就有关方面相互依赖获得了信息。
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.
本新闻发布可能包含前瞻性声明和其他陈述,而不是历史事实。前瞻性声明通常用诸如“将”、“可能”、“应该”、“预期”和类似表达方式来识别。本发布中包含的所有陈述,除历史事实陈述外,包括但不限于有关公司未来计划和目标的陈述,都是有风险和不确定性的前瞻性声明。不保证这类声明会证明是准确的,实际结果和未来事件可能会与这类声明所预期的有所不同。可能导致实际结果与公司预期不同的重要因素包括本新闻发布所述各方的风险以及其他风险和不确定性,其许多情况超出公司的控制范围。因此,公司不能保证上述事件将按照此处或全部披露的条款发生,也不能保证时间的履行。本新闻发布中包含的前瞻性声明明确受到此警告声明的约束。本新闻发布中包含的前瞻性声明是截至本新闻发布日期所述的,公司将根据加拿大证券法的规定明确更新或修订包含在其中的任何前瞻性声明。