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MindBio Begins Landmark Phase 2B Take-Home Microdosing (MB22001) Clinical Trial in Patients With Major Depressive Disorder

MindBio Begins Landmark Phase 2B Take-Home Microdosing (MB22001) Clinical Trial in Patients With Major Depressive Disorder

MindBio开始针对重度抑郁症患者的具有里程碑意义的2B期微剂量(MB22001)临床试验
Accesswire ·  03/20 04:50
  • First doses of MB22001 administered in Phase 2B take-home trial in patients with Major Depressive Disorder.

  • Follows successful Phase 2A trial where 53% of depressed patients were in complete remission from their depression at week 8 marked by a mean 14.1 point drop in MADRS score (Montgomery-Asberg Depression Rating Scale), a 60% mean drop in depressive symptoms.

  • 在针对重度抑郁症患者的 2B 期带回家试验中,第一剂 MB22001。

  • 此前成功进行了2A期试验,其中53%的抑郁症患者在第8周完全缓解了抑郁症,其标志是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,抑郁症状平均下降了60%。

VANCOUVER, BC / ACCESSWIRE / March 20, 2024 / MindBio Therapeutics Corp. (CSE:MBIO)(Frankfurt:WF6), (the "Company" or "MindBio") is pleased to announce first dosing has begun in a Phase 2B randomised controlled clinical trial microdosing MB22001 in patients with Major Depressive Disorder.

不列颠哥伦比亚省温哥华/ACCESSWIRE/2024年3月20日/ MindBio Therapeutics Corp.(CSE: MBIO)(法兰克福:WF6)(“公司” 或 “MindBio”)欣然宣布,一项针对重度抑郁症患者的微剂量 MB22001 的2B期随机对照临床试验已开始首次给药。

In a world first series of clinical trials, MindBio has secured regulatory and ministerial approvals for MB22001 to be self-administered by participants out in the community and at home. In this Phase 2B randomised, triple blind and active placebo-controlled trial, patients with major depressive disorder (MDD) will undertake an 8 week regimen of MindBio's lead candidate drug, MB22001, a proprietary titratable and self-administered form of Lysergic Acid Diethylamide (LSD) designed for take-home use. In this trial (n=90) half the participants will take an active placebo and the other half will take MB22001. After the 8 week trial, both placebo and drug group participants will be invited to participate in an 8 week open-label extension to ensure the placebo group has the opportunity to experience treatment with MB22001 resulting in potentially 16 weeks of data being collected from every patient.

在世界上第一个系列临床试验中,MindBio 已获得监管部门和部委的批准,允许社区和家中的参与者自行管理 MB22001。在这项2B期随机、三盲和活性安慰剂对照试验中,重度抑郁症(MDD)患者将接受为期8周的MindBio主要候选药物 MB22001 的疗程,这是一种专有的可滴定和自行给药的麦角酸二乙酰胺(LSD),专为带回家使用而设计。在这项试验(n=90)中,一半的参与者将服用活性安慰剂,另一半将服用 MB22001。在为期 8 周的试验结束后,安慰剂组和药物组参与者都将被邀请参加为期 8 周的开放标签延期,以确保安慰剂组有机会体验 MB22001 治疗,从而可能从每位患者那里收集 16 周的数据。

MindBio's unique investment thesis in the sector, is that small, sub-hallucinogenic doses of a psychedelic drug, MB22001 is the most scalable way to use a psychedelic medicine to treat depressive disorders globally. The Company's goal is to commercialize MB22001 as an affordable, accessible replacement to first line medications such as anti-depressants with low side effects (particularly no sexual side effects, emotional numbness, or weight gain) resulting in greater adherence to the treatment.

MindBio在该领域的独特投资论点是,小剂量的亚致幻药物,MB22001 是全球使用迷幻药物治疗抑郁症的最具可扩展性的方式。该公司的目标是将 MB22001 商业化,将其作为抗抑郁药等一线药物的一线药物的替代品,这种药物具有低副作用(特别是没有性副作用、情绪麻木或体重增加),从而提高对治疗的依从性。

Chief Executive Officer of MindBio, Justin Hanka said "Microdosing MB22001 is a disruptive treatment methodology using psychedelic medicines and our ambition is to develop this treatment globally at scale for affordable access to patients without the limitations and side-effects of common anti-depressants".

MindBio 首席执行官贾斯汀·汉卡表示:“微剂量 MB22001 是一种使用迷幻药物的颠覆性治疗方法,我们的目标是在全球范围内大规模开发这种疗法,让患者能够负担得起地获得常见抗抑郁药的限制和副作用”。

In February 2024, MindBio completed its Phase 2a trial 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 complete remission from their depression marked by an impressive mean 14.1 point drop in MADRS score (Montgomery-Asberg Depression Rating Scale). Prior trial results using MB22001 recorded statistically significant improvements in sleep quality and 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.

2024年2月,MindBio完成了针对重度抑郁症患者的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周完全缓解了抑郁症,其标志是MADRS评分(蒙哥马利-阿斯伯格抑郁评级量表)平均下降了14.1个百分点,令人印象深刻。先前使用 MB22001 的试验结果显示,睡眠质量有了统计学上的显著改善,“幸福感”、“社交联系”、“精力”、“创造力” 和 “健康” 的主观感觉有所增加,“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。

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 partipicipants, has a Phase 2a clinical trial just completed microdosing in patients with Major Depressive Disorder and a Phase 2B clinical trial currently underway microdosing in late stage cancer patients experiencing existential distress. 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已经开发了一个用于开发治疗的多学科平台,并参与迷幻药物开发和数字疗法,已经完成了对80名健康参与者的1期临床试验,一项2a期临床试验刚刚完成了对重度抑郁症患者的微剂量,目前正在进行一项2B期临床试验,对面临生存困扰的晚期癌症患者进行微剂量。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、焦虑和其他相关心理健康状况等使人衰弱的健康状况。

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SOURCE: MindBio Therapeutics

来源:MindBio Therapeutic

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