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Oragenics Develops Automated Intranasal Device for Treating Concussed Patients

Oragenics Develops Automated Intranasal Device for Treating Concussed Patients

Oragenics開發了治療腦震盪患者的自動化鼻內裝置。
Oragenics ·  06/27 12:00

Oragenics Develops Automated Intranasal Device for Treating Concussed Patients

Oragenics開發了治療腦震盪患者的自動化鼻內裝置。

June 27, 2024
2024年6月27日

The device is intended for initial treatment in the acute setting

該設備旨在用於急性階段的初步治療

SARASOTA, Fla., June 27, 2024 (GLOBE NEWSWIRE) -- Oragenics, Inc. (NYSE American: OGEN), a company focused on developing unique, intranasal pharmaceuticals for the treatment of neurological disorders, today announced it has completed a prototype of its automated intranasal device for use in concussed patients who are initially confused, dazed or unconscious in the acute phase of injury. Oragenics' lead drug candidate, ONP-002, is a new chemical entity (NCE) designed to target the brain through delivery into the nasal cavity and onward to the brain. A Phase II study is being designed to analyze the effectiveness of ONP-002 on blood biomarkers and patient-reported outcomes of concussed patients.

2024年6月27日,佛羅里達州薩拉索塔市(全球新聞採訪社)——以開發獨特的鼻內藥品治療神經系統疾病爲核心的公司Oragenics, Inc. (紐交所美國股票代碼:OGEN) 今天宣佈,已完成了用於急性階段最初混亂、失憶或昏迷的腦震盪患者的鼻內自動化裝置的原型機。Oragenics領頭藥品候選ONP-002是一種新化合物(NCE),通過將藥物輸送到鼻腔,進入大腦來目標治療大腦。正在設計第II期研究以分析ONP-002對腦震盪患者的血液生物標誌物和患者報告的療效。

Loss of consciousness along with acute memory impairment are linked to prolonged post-concussion symptoms and poor clinical outcomes. Oragenics' breath-propelled device requires the patient to administer ONP-002 into the nose. Concussed patients with an acute altered mental state may not be capable of following these instructions. Oragenics intends to use its breath-propelled device in the planned Phase II trial, which calls for multiple days of treatment. However, for those patients who have a loss of consciousness or altered mental status early on, the current automated prototype is being developed for their initial treatment by medical staff during the period in which they may struggle to follow directions for blowing.

昏迷伴隨急性記憶障礙與長時間的持續後遺症和療效不佳有關。Oragenics的噴吹裝置需要患者將ONP-002用鼻子吸入,而急性意識紊亂的患者可能無法按照說明書操作。對於那些出現意識喪失或早期意識紊亂的患者,當前自動化原型設備正在發展中,以便醫護人員在患者難以按照說明吹氣的時間內進行初始治療。

"We are excited about this new automated technology as it allows us to treat the full range of concussive injuries. Both devices offer advantages and can deliver our nanoparticle powder. Given the early mental alterations many concussed patients experience, we aim to provide them the best drug delivery route to improve their clinical outcomes," stated Michael Redmond, President at Oragenics.

“我們對這項新的自動化技術感到興奮,因爲它使我們能夠治療全範圍的腦震盪傷害。這種裝置都有各自的優勢,可以輸送我們的納米粒子粉末。由於許多腦震盪患者早期出現意識障礙,我們的目標是爲他們提供最佳的藥物遞送途徑,以改善他們的療效,” Oragenics總裁邁克爾·雷德蒙德(Michael Redmond)表示。

Approximately 10% of concussed patients lose consciousness, while many others experience an immediate altered mental state, with short-term memory loss and confusion. Both loss of consciousness and acute memory impairment are linked to prolonged post-concussion symptoms and poor clinical outcomes.

約有10%的腦震盪患者失去意識,而許多人會經歷急性意識紊亂、短期記憶喪失和混亂。昏迷伴隨急性記憶障礙,均會導致持續後遺症和療效不佳。

Concussion is an unmet medical need. There are an estimated 69 million concussions annually reported worldwide. Common causes of concussion include falls, motor vehicle accidents, and contact sports. Other neurological disorders, including Alzheimer's Disease, Parkinson's Disease, and Chronic Traumatic Encephalopathy (CTE), have been linked to concussion. Post-concussion symptomology is linked to long-term disability and occurs in as high as 20% of concussed patients.

腦震盪是一種未滿足的醫療需求。全球每年約有6900萬例腦震盪報告。腦震盪的常見原因包括跌倒、機動車事故和接觸性運動。其他神經系統疾病,包括阿爾茨海默病、帕金森病和慢性創傷性腦病(CTE)與腦震盪有關。後腦震盪症狀與長期殘疾有關,且在腦震盪患者中發生率可高達20%。

About Oragenics
www.oragenics.com

關於Oragenics
www.oragenics.com

Forward-Looking Statements
This communication contains "forward-looking statements" within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995, including without limitation statements regarding the ability of the Company to timely and successfully undertake Phase II clinical trial using its novel drug-device combination for the treatment of mild Traumatic Brain Injury. These forward-looking statements are based on management's beliefs and assumptions and information currently available. The words "believe," "expect," "anticipate," "intend," "estimate," "project" and similar expressions that do not relate solely to historical matters identify forward-looking statements. Investors should be cautious in relying on forward-looking statements because they are subject to a variety of risks, uncertainties, and other factors that could cause actual results to differ materially from those expressed in any such forward-looking statements. These factors include, but are not limited to: the Company's ability to advance the development of its product candidates, including the neurology assets, under the timelines and in accord with the milestones it projects; the Company's ability to raise capital and obtain funding, non-dilutive or otherwise, for the development of its product candidates; the regulatory application process, research and development stages, and future clinical data and analysis relating to its product candidates, including any meetings, decisions by regulatory authorities, such as the FDA and investigational review boards, whether favorable or unfavorable; the Company's ability to obtain, maintain and enforce necessary patent and other intellectual property protection; the nature of competition and development relating to concussion treatments; the Company's expectations as to the outcome of preclinical studies and clinical trials and the potential benefits, activity, effectiveness and safety of its product candidates including as to administration, transmission, manufacturing, storage and distribution; and general economic and market conditions and risks, as well as other uncertainties described in our filings with the U.S. Securities and Exchange Commission. All information set forth is as of the date hereof unless otherwise indicated. You should consider these factors in evaluating the forward-looking statements included and not place undue reliance on such statements. We do not assume any obligation to publicly provide revisions or updates to any forward-looking statements, whether as a result of new information, future developments or otherwise, should circumstances change, except as otherwise required by law.

前瞻性聲明
本通訊包含《美國私人證券訴訟改革法》中的適用的“前瞻性聲明”,包括但不限於有關公司能夠及時併成功進行Phase II臨床試驗使用其新藥物-器械組合治療輕度創傷性腦損傷的能力的聲明。這些前瞻性聲明基於管理層的信念、假設和當前可用信息。不僅與歷史事實有關的“相信”、“預期”、“預測”、“打算”、“估計”、“計劃”和類似表述詞,識別前瞻性聲明,投資者應在依靠前瞻性聲明時保持謹慎,因爲它們受到各種風險、不確定性和其他因素的影響,這些因素可能導致實際結果與任何此類前瞻性聲明中表達的結果在很大程度上不同。這些因素包括但不限於:公司能否在其所預計的時間表下並按照其所預期的里程碑推進其產品候選品,包括神經科學資產的發展;公司能否籌集資本並獲得用於開發其產品候選品的融資,無論是否爲非稀釋性;與其產品候選品有關的監管申請過程、研發階段和未來臨床數據和分析,包括任何會議、決策、如美國食品和藥物管理局和調查評審委員會之類的監管當局是否有利或不利;公司能否獲得、維護和執行必需的專利和其他知識產權保護;與腦震盪治療有關的競爭和發展;公司對臨床前和臨床試驗以及其產品候選品的其他經濟和市場條件和風險的預期以及其活動、效力和安全性;以及一般經濟和市場狀況和風險,以及其他在我們向美國證券交易委員會提交的文件中描述的不確定性。除非另有說明,這裏的所有信息均截至本日期。您應在評估所包含的前瞻性聲明時考慮這些因素,並不應對這些聲明提供任何修訂或更新,無論是因爲新信息、未來發展還是其他原因的變化,除非法律另有規定。

Oragenics, Inc.
Janet Huffman, Chief Financial Officer
813-286-7900
jhuffman@oragenics.com

Oragenics, Inc.
Janet Huffman,首席財務官
813-286-7900
jhuffman@oragenics.com

Investor Relations:
Rich Cockrell
CG Capital
404-736-3838
ogen@cg.capital

投資者關係:
Rich Cockrell
CG資本
404-736-3838
ogen@cg.capital

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Source: Oragenics

來源:Oragenics

Released June 27, 2024

2024年6月27日發佈

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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