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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開始針對重度抑鬱症患者的具有里程碑意義的2B期微劑量(MB22001)臨床試驗
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.

  • 在針對重度抑鬱症患者的 2B 期帶回家試驗中,第一劑 MB22001。

  • 此前成功進行了2A期試驗,其中53%的抑鬱症患者在第8周完全緩解了抑鬱症,其標誌是MADRS評分(蒙哥馬利-阿斯伯格抑鬱評級量表)平均下降了14.1點,抑鬱症狀平均下降了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.

不列顛哥倫比亞省溫哥華/ACCESSWIRE/2024年3月20日/ MindBio Therapeutics Corp.(CSE: MBIO)(法蘭克福:WF6)(“公司” 或 “MindBio”)欣然宣佈,一項針對重度抑鬱症患者的微劑量 MB22001 的2B期隨機對照臨床試驗已開始首次給藥。

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.

在世界上第一個系列臨床試驗中,MindBio 已獲得監管部門和部委的批准,允許社區和家中的參與者自行管理 MB22001。在這項2B期隨機、三盲和活性安慰劑對照試驗中,重度抑鬱症(MDD)患者將接受爲期8周的MindBio主要候選藥物 MB22001 的療程,這是一種專有的可滴定和自行給藥的麥角酸二乙酰胺(LSD),專爲帶回家使用而設計。在這項試驗(n=90)中,一半的參與者將服用活性安慰劑,另一半將服用 MB22001。在爲期 8 周的試驗結束後,安慰劑組和藥物組參與者都將被邀請參加爲期 8 周的開放標籤延期,以確保安慰劑組有機會體驗 MB22001 治療,從而可能從每位患者那裏收集 16 周的數據。

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在該領域的獨特投資論點是,小劑量的亞致幻藥物,MB22001 是全球使用迷幻藥物治療抑鬱症的最具可擴展性的方式。該公司的目標是將 MB22001 商業化,將其作爲抗抑鬱藥等一線藥物的一線藥物的替代品,這種藥物具有低副作用(特別是沒有性副作用、情緒麻木或體重增加),從而提高對治療的依從性。

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 首席執行官賈斯汀·漢卡表示:“微劑量 MB22001 是一種使用迷幻藥物的顛覆性治療方法,我們的目標是在全球範圍內大規模開發這種療法,讓患者能夠負擔得起地獲得常見抗抑鬱藥的限制和副作用”。

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完成了針對重度抑鬱症患者的2a期試驗。在這項開放標籤試驗中,患者的抑鬱症狀下降了60%,進入MDD試驗的患者中有53%在第8周完全緩解了抑鬱症,其標誌是MADRS評分(蒙哥馬利-阿斯伯格抑鬱評級量表)平均下降了14.1個百分點,令人印象深刻。先前使用 MB22001 的試驗結果顯示,睡眠質量有了統計學上的顯著改善,“幸福感”、“社交聯繫”、“精力”、“創造力” 和 “健康” 的主觀感覺有所增加,“憤怒” 和 “煩躁” 減少了。MB22001 是一種治療抑鬱症的前景和潛在的市場顛覆性藥物。

About MindBio Therapeutics

關於 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是一家領先的生物技術/生物製藥公司,專注於爲心理健康問題創造新的和新興的治療方法,並且正在進行世界上第一個帶回家的微劑量(MB22001)人體臨床試驗。MB22001 是 MindBio 的主要候選藥物,一種專有的可滴定形式的麥角酸二乙酰胺 (LSD),專爲帶回家的微劑量而設計。MindBio是迷幻藥物微劑量的領導者,正在通過臨床試驗推進其藥物和技術方案。MindBio已經開發了一個用於開發治療的多學科平台,並參與迷幻藥物開發和數字療法,已經完成了對80名健康參與者的1期臨床試驗,一項2a期臨床試驗剛剛完成了對重度抑鬱症患者的微劑量,目前正在進行一項2B期臨床試驗,對面臨生存困擾的晚期癌症患者進行微劑量。MindBio投資的研究爲開發經臨床驗證的新療法奠定了基礎,包括數字技術和干預措施,以治療抑鬱、焦慮和其他相關心理健康狀況等使人衰弱的健康狀況。

Cautionary Note Concerning Forward-Looking Statements:

關於前瞻性陳述的警示性說明:

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.

該新聞稿包含適用證券法所指的 “前瞻性陳述”。前瞻性陳述可以通過以下詞語來識別:“預期”、“打算”、“預算”、“相信”、“項目”、“估計”、“預期”、“預期”、“戰略”、“未來”、“可能”、“可能”、“會”、“應該”、“將” 以及對未來時期或負面時期的類似提法或類似的術語, 以及將來通常使用的術語和有條件的術語.前瞻性陳述基於截至提供之日的假設。但是,無法保證此類假設會反映這些項目或因素的實際結果。

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,一些已知和未知的風險因素可能導致公司的實際業績和財務狀況與前瞻性陳述中指出的業績和財務狀況存在重大差異。因此,您不應依賴這些前瞻性陳述中的任何一項。可能導致實際業績和財務狀況與前瞻性陳述中所述業績和財務狀況存在重大差異的重要風險因素包括:加拿大和澳大利亞的總體經濟、市場和商業狀況;市場波動;本新聞稿中描述的任何交易或事件的時間表出現不可預見的延遲。本警示聲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,否則公司沒有義務修改或更新任何此類前瞻性陳述,也沒有義務公開宣佈對本文包含的任何前瞻性信息進行任何修訂的結果,以反映未來的業績、事件或發展。

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.

加拿大證券交易所及其監管服務提供商(該術語在加拿大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。

SOURCE: MindBio Therapeutics

來源:MindBio Therapeutic

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