MindBio Is Exploring Dual Listing on A Senior Exchange With Multiple Phase 2B Clinical Trials Underway Supported by Positive Trial Data and Planning for Phase 3
MindBio Is Exploring Dual Listing on A Senior Exchange With Multiple Phase 2B Clinical Trials Underway Supported by Positive Trial Data and Planning for Phase 3
VANCOUVER, BC / ACCESSWIRE / May 1, 2024 / MindBio Therapeutics Corp. (CSE:MBIO)(Frankfurt:WF6), (the "Company" or "MindBio"), is pleased to announce that it has been presenting MindBio to various parties, institutional investment firms and brokerage firms for a potential dual listing on a senior exchange in the United States or Australia.
不列颠哥伦比亚省温哥华/ACCESSWIRE/2024年5月1日/MindBio Therapeutics Corp.(CSE: MBIO)(法兰克福:WF6)(“公司” 或 “MindBio”)欣然宣布,它已向各方、机构投资公司和经纪公司介绍MindBio,以在美国或澳大利亚的高级交易所进行双重上市。
The Company has successfully completed Phase 1 and Phase 2a Clinical Trials with positive readouts and new discoveries. In February 2024, MindBio completed its Phase 2a trial of MB22001 in patients with Major Depressive Disorder. In this open label trial, patients experienced a 60% drop in depressive symptoms and 53% of patients entering the trial with MDD, at week 8 were in remission from their depression with a mean 14.1 point drop in MADRS score (Montgomery-Asberg Depression Rating Scale). Prior trial results using MB22001 recorded statistically significant improvements in total sleep time and quality of sleep and statistically significant increases in subjective feelings of "Happiness", "Social Connectivity", "Energy", "Creativity" and "Wellness" with reduced "Anger" and "Irritability". MB22001 is a promising and potential market disruptive medicine for treating depressive illness.
该公司已成功完成了1期和2a期临床试验,取得了积极的读数和新的发现。2024 年 2 月,MindBio 完成了针对重度抑郁症患者的 MB22001 2a 期试验。在这项开放标签试验中,患者的抑郁症状下降了60%,进入MDD试验的患者中有53%在第8周缓解了抑郁症,MADRS评分(蒙哥马利-阿斯伯格抑郁评级量表)平均下降了14.1点。先前使用 MB22001 的试验结果显示,总睡眠时间和睡眠质量有统计学上的显著改善,“幸福感”、“社交联系”、“精力”、“创造力” 和 “健康” 的主观感受在统计学上显著增加,“愤怒” 和 “烦躁” 减少了。MB22001 是一种治疗抑郁症的前景和潜在的市场颠覆性药物。
The Company is now running two significant Phase 2B clinical trials with dosing underway and a third Phase 2B trial that has now also been approved in women's health. In a series of world firsts, each of these trials is approved for the take-home use of MB22001, a proprietary and self-titratable form of Lysergic Acid Diethylamide (LSD) designed for safe take home microdosing.
该公司目前正在进行两项重要的2B期临床试验,正在进行给药,以及第三项2B期试验,该试验现已在女性健康领域获得批准。在一系列世界首创中,这些试验均获准带回家 MB22001,这是一种专有的可自滴定形式的麦角酸二乙酰胺(LSD),专为安全带回家的微剂量而设计。
MindBio will publish further readouts of its Phase 1 and 2A results in 2024 and expects the results of its Phase 2B trials to be announced in 2025. Management is now preparing and is in discussions with Clinical Research Organizations (CROs) for Phase 3 Clinical Trials with a 2025 start.
MindBio将在2024年发布其1期和2A期结果的更多读数,并预计其2B期试验的结果将在2025年公布。管理层目前正在为2025年开始的3期临床试验做准备并正在与临床研究组织(CRO)进行讨论。
There are only a handful of public companies in the world that have progressed to Phase 2 and Phase 3 clinical trials in psychedelic medicines. MindBio is the most advanced clinical trial stage biopharma company listed on the Canadian Securities Exchange and the only company at this level that is not listed on a senior exchange. Given the success of its clinical trials and current program of works underway with multiple Phase 2B randomized controlled trials, management is actively having meetings with investment groups in Canada, United States and Australia for a potential dual listing on a senior exchange.
世界上只有少数几家上市公司已进入迷幻药物的2期和3期临床试验。MindBio是加拿大证券交易所上市的最先进的临床试验阶段生物制药公司,也是唯一一家未在高级交易所上市的该级别的公司。鉴于其临床试验的成功以及目前正在进行的多项2B期随机对照试验的工作计划,管理层正在积极与加拿大、美国和澳大利亚的投资集团举行会议,讨论可能在优先交易所双重上市的问题。
The Company will provide further updates to the market.
该公司将向市场提供进一步的最新信息。
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About MindBio Therapeutics
关于 MindBio Therape
MindBio is a leading biotech/biopharma company focused on creating novel and emerging treatments for mental health conditions and is conducting world first take-home Microdosing (MB22001) human clinical trials. MB22001 is MindBio's lead candidate drug, a proprietary titratable form of Lysergic Acid Diethylamide (LSD) designed for take-home microdosing. MindBio is a leader in microdosing of psychedelic medicines and is advancing its drug and technology protocols through clinical trials. MindBio has developed a multi-disciplinary platform for developing treatments and is involved in psychedelic medicine development and digital therapeutics, has completed Phase 1 clinical trials in 80 healthy participants and has completed a Phase 2a clinical trial in patients with Major Depressive Disorder, both trials with positive top line data reported. Currently underway are two Phase 2B trials, one in cancer patients experiencing existential distress and another in patients with Major Depressive Disorder. MindBio invests in research that forms the basis for developing novel and clinically proven treatments including digital technologies and interventions to treat debilitating health conditions such as depression, anxiety and other related mental health conditions.
MindBio是一家领先的生物技术/生物制药公司,专注于为心理健康问题创造新的和新兴的治疗方法,并且正在进行世界上第一个带回家的微剂量(MB22001)人体临床试验。MB22001 是 MindBio 的主要候选药物,一种专有的可滴定形式的麦角酸二乙酰胺 (LSD),专为带回家的微剂量而设计。MindBio是迷幻药物微剂量的领导者,正在通过临床试验推进其药物和技术方案。MindBio开发了用于开发治疗的多学科平台,参与迷幻药物开发和数字疗法,已完成了对80名健康参与者的1期临床试验,并完成了针对重度抑郁症患者的2a期临床试验,这两项试验均报告了积极的顶线数据。目前正在进行两项2B期试验,一项针对经历生存困扰的癌症患者,另一项针对重度抑郁症患者。MindBio投资的研究为开发经临床验证的新疗法奠定了基础,包括数字技术和干预措施,以治疗抑郁、焦虑和其他相关的心理健康状况等使人衰弱的健康状况。
Cautionary Note Concerning Forward-Looking Statements:
关于前瞻性陈述的警示性说明:
The press release contains "forward-looking statements" within the meaning of applicable securities laws. Forward-looking statements can be identified by words such as: "anticipate," "intend," "plan," "budget," "believe," "project," "estimate," "expect," "scheduled," "forecast," "strategy," "future," "likely," "may," "to be," "could," "would," "should," "will" and similar references to future periods or the negative or comparable terminology, as well as terms usually used in the future and conditional. Forward-looking statements are based on assumptions as of the date they are provided. However, there can be no assurance that such assumptions will reflect the actual outcome of such items or factors.
该新闻稿包含适用证券法所指的 “前瞻性陈述”。前瞻性陈述可以通过以下词语来识别:“预期”、“打算”、“预算”、“相信”、“项目”、“估计”、“预期”、“预期”、“战略”、“未来”、“可能”、“可能”、“会”、“应该”、“将” 以及对未来时期或负面时期的类似提法或类似的术语, 以及将来通常使用的术语和有条件的术语.前瞻性陈述基于截至提供之日的假设。但是,无法保证此类假设会反映这些项目或因素的实际结果。
Additionally, there are known and unknown risk factors that could cause the Company's actual results and financial conditions to differ materially from those indicated in the forward-looking statements. Therefore, you should not rely on any of these forward-looking statements. Important risk factors that could cause actual results and financial conditions to differ materially from those indicated in the forward-looking statements, include among others: general economic, market and business conditions in Canada and Australia; market volatility; unforeseen delays in timelines for any of the transactions or events described in this press release. All forward-looking information is qualified in its entirety by this cautionary statement.
此外,一些已知和未知的风险因素可能导致公司的实际业绩和财务状况与前瞻性陈述中指出的业绩和财务状况存在重大差异。因此,您不应依赖这些前瞻性陈述中的任何一项。可能导致实际业绩和财务状况与前瞻性陈述中所述业绩和财务状况存在重大差异的重要风险因素包括:加拿大和澳大利亚的总体经济、市场和商业状况;市场波动;本新闻稿中描述的任何交易或事件的时间表出现不可预见的延迟。本警示声明完全限定了所有前瞻性信息。
The Company disclaims any obligation to revise or update any such forward-looking statement or to publicly announce the result of any revisions to any of the forward-looking information contained herein to reflect future results, events or developments, except as required by law.
除非法律要求,否则公司没有义务修改或更新任何此类前瞻性陈述,也没有义务公开宣布对本文包含的任何前瞻性信息进行任何修订的结果,以反映未来的业绩、事件或发展。
Neither the Canadian Securities Exchange nor its Regulation Service Provider (as that term is defined in the policies of the Canadian Securities Exchange) accepts responsibility for the adequacy or accuracy of this release.
加拿大证券交易所及其监管服务提供商(该术语在加拿大证券交易所的政策中定义)均不对本新闻稿的充分性或准确性承担责任。
SOURCE: MindBio Therapeutics
来源:MindBio Therapeutic