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Oragenics Develops Automated Intranasal Device for Treating Concussed Patients

Oragenics Develops Automated Intranasal Device for Treating Concussed Patients

Oragenics开发了治疗脑震荡患者的自动化鼻内装置。
Oragenics ·  06/27 00:00

Oragenics Develops Automated Intranasal Device for Treating Concussed Patients

Oragenics开发了治疗脑震荡患者的自动化鼻内装置。

June 27, 2024
2024年6月27日

The device is intended for initial treatment in the acute setting

该设备旨在用于急性阶段的初步治疗

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,佛罗里达州萨拉索塔市(全球新闻采访社)——以开发独特的鼻内药品治疗神经系统疾病为核心的公司Oragenics, Inc. (纽交所美国股票代码:OGEN) 今天宣布,已完成了用于急性阶段最初混乱、失忆或昏迷的脑震荡患者的鼻内自动化装置的原型机。Oragenics领头药品候选ONP-002是一种新化合物(NCE),通过将药物输送到鼻腔,进入大脑来目标治疗大脑。正在设计第II期研究以分析ONP-002对脑震荡患者的血液生物标志物和患者报告的疗效。

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.

昏迷伴随急性记忆障碍与长时间的持续后遗症和疗效不佳有关。Oragenics的喷吹装置需要患者将ONP-002用鼻子吸入,而急性意识紊乱的患者可能无法按照说明书操作。对于那些出现意识丧失或早期意识紊乱的患者,当前自动化原型设备正在发展中,以便医护人员在患者难以按照说明吹气的时间内进行初始治疗。

"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.

“我们对这项新的自动化技术感到兴奋,因为它使我们能够治疗全范围的脑震荡伤害。这种装置都有各自的优势,可以输送我们的纳米粒子粉末。由于许多脑震荡患者早期出现意识障碍,我们的目标是为他们提供最佳的药物递送途径,以改善他们的疗效,” Oragenics总裁迈克尔·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.

约有10%的脑震荡患者失去意识,而许多人会经历急性意识紊乱、短期记忆丧失和混乱。昏迷伴随急性记忆障碍,均会导致持续后遗症和疗效不佳。

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.

脑震荡是一种未满足的医疗需求。全球每年约有6900万例脑震荡报告。脑震荡的常见原因包括跌倒、机动车事故和接触性运动。其他神经系统疾病,包括阿尔茨海默病、帕金森病和慢性创伤性脑病(CTE)与脑震荡有关。后脑震荡症状与长期残疾有关,且在脑震荡患者中发生率可高达20%。

About Oragenics
www.oragenics.com

关于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.

前瞻性声明
本通讯包含《美国私人证券诉讼改革法》中的适用的“前瞻性声明”,包括但不限于有关公司能够及时并成功进行Phase II临床试验使用其新药物-器械组合治疗轻度创伤性脑损伤的能力的声明。这些前瞻性声明基于管理层的信念、假设和当前可用信息。不仅与历史事实有关的“相信”、“预期”、“预测”、“打算”、“估计”、“计划”和类似表述词,识别前瞻性声明,投资者应在依靠前瞻性声明时保持谨慎,因为它们受到各种风险、不确定性和其他因素的影响,这些因素可能导致实际结果与任何此类前瞻性声明中表达的结果在很大程度上不同。这些因素包括但不限于:公司能否在其所预计的时间表下并按照其所预期的里程碑推进其产品候选品,包括神经科学资产的发展;公司能否筹集资本并获得用于开发其产品候选品的融资,无论是否为非稀释性;与其产品候选品有关的监管申请过程、研发阶段和未来临床数据和分析,包括任何会议、决策、如美国食品和药物管理局和调查评审委员会之类的监管当局是否有利或不利;公司能否获得、维护和执行必需的专利和其他知识产权保护;与脑震荡治疗有关的竞争和发展;公司对临床前和临床试验以及其产品候选品的其他经济和市场条件和风险的预期以及其活动、效力和安全性;以及一般经济和市场状况和风险,以及其他在我们向美国证券交易委员会提交的文件中描述的不确定性。除非另有说明,这里的所有信息均截至本日期。您应在评估所包含的前瞻性声明时考虑这些因素,并不应对这些声明提供任何修订或更新,无论是因为新信息、未来发展还是其他原因的变化,除非法律另有规定。

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

Oragenics, Inc.
Janet Huffman,首席财务官
813-286-7900
jhuffman@oragenics.com

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

投资者关系:
Rich Cockrell
CG资本
404-736-3838
ogen@cg.capital

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Source: Oragenics

来源:Oragenics

Released June 27, 2024

2024年6月27日发布

声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
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