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Pasithea Therapeutics Announces Results of Preclinical Study Demonstrating Tolerizing Vaccine Efficacy in Relapsing-Remitting Model of Multiple Sclerosis

Pasithea Therapeutics Announces Results of Preclinical Study Demonstrating Tolerizing Vaccine Efficacy in Relapsing-Remitting Model of Multiple Sclerosis

Pasithea治療公司宣佈臨牀前研究結果顯示耐受性疫苗對多發性硬化症復發-緩解模型的療效
GlobeNewswire ·  2022/08/11 08:17

-- PAS002 is a proprietary DNA tolerizing vaccine construct encoding GlialCAM --
-- PAS002 effectively reduces disease severity, delays onset of illness, while also reducing relapse severity --
-- GlialCAM fragment is present in monkeypox virus, supporting a potential role in current vaccine development --

--PAS002是一種編碼GlialCAM的專有DNA耐受疫苗構造--
--PAS002有效地降低了疾病的嚴重程度,推遲了疾病的發病,同時還降低了復發的嚴重程度--
--猴痘病毒中存在GlialCAM片段,支持在當前疫苗開發中發揮潛在作用--

MIAMI BEACH, Fla., Aug. 11, 2022 (GLOBE NEWSWIRE) -- Pasithea Therapeutics Corp. (Nasdaq: KTTA) ("Pasithea" or the "Company"), a biotechnology company focused on the discovery, research and development of new and effective treatments for psychiatric and neurological disorders, today announced positive results from a preclinical proof of concept study of PAS002, its tolerizing vaccine program in multiple sclerosis ("MS").  

環球通訊社佛羅裏達州邁阿密海灘,2022年8月11日-專注於發現、研究和開發治療精神和神經疾病的新型有效療法的生物技術公司Pasithea Treateutics Corp.(納斯達克代碼:KTTA)今天宣佈,其治療多發性硬化症(MS)的耐受性疫苗計劃PAS002的臨牀前概念驗證研究取得了積極結果。

Earlier this year, a study in Nature, the world's leading science journal, showed that a molecule called GlialCAM found in the brain's white matter is attacked in MS. GlialCAM shares a component of its protein structure that mimics an identical component of the Epstein Barr Virus ("EBV") Nuclear Antigen-1, which plays a critical role in triggering MS.

今年早些時候,世界領先的科學雜誌《自然》上的一項研究表明,在大腦白質中發現的一種名為GlialCAM的分子受到了攻擊,GlialCAM與其蛋白質結構中的一個成分相似,該成分與愛潑斯坦-巴爾病毒(EBV)核抗原-1的成分相同,後者在引發多發性硬化症中起着關鍵作用。

In this proof of concept study, relapsing paralysis was established in a mouse model of relapsing-remitting experimental autoimmune encephalomyelitis ("EAE"), the standard animal model of MS. In three groups, a proprietary DNA cassette was engineered to encode GlialCAM and injected to potentially block acute disease and its relapse. These DNA molecules were designed to protect against paralytic disease by tolerizing the immune system so it would not attack myelin in the brain and spinal cord. The engineered DNA molecule creates tolerance, working like an 'inverse vaccine', and was administered intra-muscularly at days 0, 3, 7, 10, and 14. The study had a standard duration of 32 days.

在這項概念驗證研究中,在復發-緩解性實驗性自身免疫性腦脊髓炎(“EAE”)的小鼠模型上建立了複發性癱瘓,EAE是MS的標準動物模型。在三組中,設計了一種專有的DNA盒來編碼GlialCAM並注射,以潛在地阻止急性疾病及其復發。這些DNA分子被設計成通過耐受免疫系統來預防癱瘓疾病,這樣它就不會攻擊大腦和脊髓中的髓鞘。這種經過改造的DNA分子可以產生耐受性,就像一種“反向疫苗”,在第0天、第3天、第7天、第10天和第14天肌肉注射。這項研究的標準持續時間為32天。

The data showed that the engineered DNA plasmids provide a high level of efficacy in reducing disease severity and incidence of relapse when administered prophylactically in the EAE model, a widely used relapsing-remitting model of MS.

數據顯示,當在廣泛使用的MS復發-緩解模型EAE模型中預防性給藥時,工程DNA質粒在降低疾病嚴重性和複發率方面提供了高水平的療效。

Key findings from the study include:

這項研究的主要發現包括:

  • treatment with a DNA tolerizing 'inverse vaccine' delayed the onset of paralysis when compared to vehicle (p<0.001);
  • a statistically significant reduction in disease severity, when compared to vehicle (p=0.002);
  • a statistically significant reduction in relapse severity, when compared to vehicle (p<0.001);
  • treatment with a DNA vaccine prevented disease in approximately 50% of the mice, when compared to vehicle (p=0.004).
  • 與賦形劑相比,耐受DNA反向疫苗的治療延遲了癱瘓的發生(p
  • 與車輛相比,疾病嚴重程度在統計學上顯著降低(p=0.002);
  • 與Vehicle相比,復發嚴重程度在統計上顯著降低(p
  • 與使用藥物相比,使用DNA疫苗治療可以預防大約50%的小鼠的疾病(p=0.004)。

The study was conducted at Hooke Laboratories, an independent full-service Contract Research Organization with deep experience in the EAE animal model of MS.

這項研究是在胡克實驗室進行的,這是一家獨立的全方位服務合同研究機構,在MS的EAE動物模型方面擁有豐富的經驗。

"The results of this study show that this technology has the potential to tolerize to GlialCAM, a myelin molecule that has molecular similarity to the Epstein Barr Virus that triggers MS," stated Pasithea's Chairman, National Academy of Sciences Professor Lawrence Steinman, a world recognized leading authority in MS. Prof. Steinman's research led to the development of the drug Tysabri, which is approved to treat patients with MS and Crohn's disease. "Remarkably, the piece of GlialCAM protein shared between EBV and white matter in the brain is also found in the pox viruses, including monkeypox. Monkeypox is rarely associated with brain inflammation, and this new technology may prove useful as a treatment for brain inflammation caused in certain viral infections."

Pasithea主席、國家科學院主席勞倫斯·斯坦曼教授説:“這項研究的結果表明,這項技術有可能耐受GlialCAM,這是一種與引發多發性硬化症的愛潑斯坦-巴爾病毒具有分子相似性的髓鞘分子。”斯坦曼教授是世界公認的領先權威,他的研究導致了藥物Tysabri的開發,該藥物被批准用於治療多發性硬化症和克羅恩病患者。值得注意的是,EB病毒和大腦中白質共享的GlialCAM蛋白片段也在猴痘病毒中發現。猴痘病毒很少與腦部炎症有關,這項新技術可能會被證明對治療某些病毒感染引起的腦部炎症很有用。

Dr. Tiago Reis Marques, Chief Executive Officer of Pasithea, stated, "We're thrilled with the strong preclinical efficacy data shown in this study. Although early stage, we believe these results demonstrate the promise and validity of our tolerizing approach, which is built on recent data on the biological mechanism linking infection with EBV with the development of MS. We have filed a provisional patent application and we will continue to rapidly pursue the PAS002 drug development program."

Pasithea公司首席執行官蒂亞戈·里斯·馬奎斯博士説:“我們對這項研究中顯示的強大的臨牀前療效數據感到興奮。雖然還處於早期階段,但我們相信這些結果證明瞭我們耐受性方法的前景和有效性,這種方法建立在有關EB病毒感染與多發性硬化症發病之間的生物學機制的最新數據的基礎上。我們已經提交了臨時專利申請,我們將繼續快速推進PAS002藥物開發計劃。”

The Company plans to present data from this study, including histology data and plasma inflammatory markers, in future major international conferences, and also to submit full data for peer-review publication.

該公司計劃在未來的主要國際會議上公佈這項研究的數據,包括組織學數據和血漿炎症標誌物,並提交完整的數據供同行評審發表。

About Multiple Sclerosis

關於多發性硬化症

Multiple Sclerosis ("MS") is a chronic and potentially disabling autoimmune disease, and the most common neurodegenerative disease of the central nervous system in young adults. The pathological hallmark of MS is the formation of demyelinating lesions in the brain and spinal cord, with the immune system attacking the myelin sheath that normally protects nerve fibers in the brain, spinal cord, and optic nerve. There are now 2.8 million people worldwide who have MS, and every five minutes, someone, somewhere in the world is diagnosed with this disorder. While there is no way to predict with any certainty how an individual's disease will progress, four basic MS disease courses (also called types or phenotypes) have been defined: clinically isolated syndrome, relapsing remitting, secondary progressive and primary progressive. The most common affecting around 85 per cent of everyone diagnosed with MS is relapsing remitting MS (RRMS). It means that symptoms appear (a relapse), and then fade away, either partially or completely (remitting).

多發性硬化症(MS)是一種慢性的、可能致殘的自身免疫性疾病,也是年輕人最常見的中樞神經系統退行性疾病。多發性硬化症的病理特徵是在大腦和脊髓形成脱髓鞘病變,免疫系統攻擊通常保護大腦、脊髓和視神經的髓鞘。現在全世界有280萬人患有多發性硬化症,每五分鐘,世界上某個地方的某個人就會被診斷出患有這種疾病。雖然沒有辦法確切地預測一個人的疾病將如何發展,但已經定義了四種基本的MS疾病病程(也稱為類型或表型):臨牀孤立綜合徵、復發緩解、繼發性進展性和原發進展性。最常見的影響大約85%被診斷為多發性硬化症的人是復發緩解性多發性硬化症(RRMS)。這意味着症狀出現(復發),然後消失,部分或完全(緩解)。

ABOUT PAS002

關於PAS002

PAS002 is an engineered DNA plasmid designed to tolerize the immune system to GlialCAM.

PAS002是一種設計用於耐受GlialCAM的免疫系統的工程DNA質粒。

About Pasithea Therapeutics Corp.

Pasithea治療公司簡介

Pasithea Therapeutics Corporation is a U.S. biotechnology company focused on the discovery, research and development of new and effective treatments for psychiatric and neurological disorders. With an experienced team of experts in the fields of neuroscience and psychopharmacology, Pasithea is developing new molecular entities for the treatment of psychiatric and neurological disorders. Pasithea is also focused on addressing the needs of patients currently suffering with mental illness by providing access to IV ketamine infusions both in clinics and in-home settings.

Pasithea治療公司是一家美國生物技術公司,專注於發現、研究和開發治療精神和神經疾病的新的有效療法。Pasithea擁有一支在神經科學和精神藥理學領域經驗豐富的專家團隊,正在開發用於治療精神和神經疾病的新分子實體。Pasithea還專注於通過在診所和家庭環境中提供靜脈注射氯胺酮來滿足目前患有精神疾病的患者的需求。

Forward Looking Statements

前瞻性陳述

This press release contains statements that constitute "forward-looking statements." Forward-looking statements are subject to numerous conditions, many of which are beyond the control of the Company. While the Company believes these forward-looking statements are reasonable, undue reliance should not be placed on any such forward-looking statements, which are based on information available to the Company on the date of this release. These forward-looking statements are based upon current estimates and assumptions and are subject to various risks and uncertainties, including, without limitation, those set forth in the Company's filings with the SEC. Thus, actual results could be materially different. The Company undertakes no obligation to update these statements whether as a result of new information, future events or otherwise, after the date of this release, except as required by law.

本新聞稿包含構成“前瞻性陳述”的陳述。前瞻性陳述受許多條件的制約,其中許多條件不在公司的控制範圍之內。雖然公司相信這些前瞻性陳述是合理的,但不應過度依賴任何此類前瞻性陳述,這些前瞻性陳述是基於公司在本新聞稿發佈之日所掌握的信息。這些前瞻性陳述是基於當前的估計和假設,會受到各種風險和不確定性的影響,包括但不限於公司提交給美國證券交易委員會的報告中陳述的風險和不確定性。因此,實際結果可能會有很大不同。除法律要求外,本公司不承擔在本新聞稿發佈之日後因新信息、未來事件或其他原因而更新這些陳述的義務。

Pasithea Therapeutics Corp. Company Contact
Dr. Tiago Reis Marques
Chief Executive Officer
E: tiago@pasithea.com

Pasithea治療公司聯繫人
蒂亞戈·里斯·馬奎斯博士
首席執行官
電子郵件:tiago@pasithea.com

Pasithea Therapeutics Corp. Investor Relations
Lisa M. Wilson
In-Site Communications, Inc.
T: 212-452-2793
E: lwilson@insitecony.com

Pasithea治療公司投資者關係
麗莎·M·威爾遜
現場通信公司
T: 212-452-2793
電子郵箱:lwilson@insiteconi.com


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