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Odyssey Health Achieves Positive Safety Outcomes for Concussion Drug in Multiple Ascending Dosing Trial, Cohort II

Odyssey Health Achieves Positive Safety Outcomes for Concussion Drug in Multiple Ascending Dosing Trial, Cohort II

奧德賽健康公司在多劑量遞增試驗中取得積極的震盪藥物安全結果,隊列II
GlobeNewswire ·  2022/09/13 08:07

Las Vegas, NV, Sept. 13, 2022 (GLOBE NEWSWIRE) -- Odyssey Health, Inc. (OTC: ODYY), f/k/a Odyssey Group International, Inc., a company focused on developing unique, life-enhancing medical products, today announced the successful completion of safety measures for the second cohort of their Phase I Multi-Day Ascending Dosing (MAD) clinical trial. Odyssey's trial involves administering PRV-002, the Company's novel drug to treat concussion, to healthy human subjects to determine drug safety. For all cohorts of the trial, the drug was found to be safe and well tolerated.

內華達州拉斯維加斯,9月2022年12月13日(環球網)--奧德賽健康公司(場外交易代碼:ODYY),f/k/a奧德賽集團國際公司,一家專注於開發獨特的、提高生命的醫療產品的公司,今天宣佈,他們的第一階段多天遞增劑量(MAD)臨牀試驗的第二個隊列的安全措施成功完成。奧德賽公司的試驗涉及給健康人服用該公司治療腦震盪的新藥PRV-002,以確定藥物安全性。在試驗的所有隊列中,該藥物被發現是安全的,耐受性良好。

The Phase I MAD clinical trial consists of a total of 16 healthy subjects. In Cohort I, eight patients received a low dose of drug and in Cohort II, patients received a high dose of drug. In both cohorts the drug was well tolerated and safe with no severe adverse events reported.

MAD一期臨牀試驗共16名健康受試者。在隊列I中,8名患者接受了低劑量的藥物治療,在隊列II中,患者接受了高劑量的藥物治療。在這兩個隊列中,該藥物耐受性和安全性都很好,沒有嚴重不良事件的報道。

Michael Redmond, CEO of Odyssey Health, Inc. commented, "At double the dose of the previous cohort we saw no serious adverse events. As we come close to completing the Phase I trial, I am very pleased with the safety profile of our concussion pharmaceutical treatment, PRV-002. I'm equally pleased that the intranasal drug/device combination has functioned nicely and has been easy to operate in the clinical setting."

奧德賽健康公司首席執行官邁克爾·雷德蒙德評論説:“我們的劑量是前一組的兩倍,我們沒有發現嚴重的不良反應。隨着我們接近完成第一階段試驗,我對我們的腦震盪藥物PRV-002的安全性感到非常滿意。我同樣感到高興的是,鼻腔藥物/裝置組合運行良好,在臨牀環境中易於操作。”

Odyssey is currently selecting clinical sites and developing the Investigator's Brochure for the Phase II trial. Concussions represent an 'unmet' medical need and affect millions worldwide. Repetitive concussions can lead to rapid cognitive decline and emotional lability.

奧德賽公司目前正在選擇臨牀地點,併為第二階段試驗開發研究人員手冊。腦震盪代表着一種未得到滿足的醫療需求,影響着全球數百萬人。反覆腦震盪會導致認知能力迅速下降和情緒不穩定。

The global market for concussion treatment was valued at $6.9 billion in 2020 and is forecasted to reach $8.9 billion by 2027, according to Grandview Research.

根據Grandview Research的數據,2020年,全球腦震盪治療市場的價值為69億美元,預計到2027年將達到89億美元。

About Odyssey Health Inc. (formerly Odyssey Group International, Inc.)
Odyssey Health Inc. (OTC: ODYY) is a medical company with a focus in the area of life-saving medical solutions. Odyssey's corporate mission is to create, acquire and develop distinct assets, intellectual property, and exceptional technologies that provide meaningful medical solutions. The company is focused on areas that have an identified technological advantage, provide superior clinical utility, and have a substantial market opportunity. For more information, visit the company's website at

關於奧德賽健康公司(前身為奧德賽國際集團)
奧德賽健康公司(場外交易代碼:ODYY)是一家專注於拯救生命的醫療解決方案領域的醫療公司。奧德賽的公司使命是創造、收購和開發獨特的資產、知識產權和特殊技術,提供有意義的醫療解決方案。該公司專注於具有公認的技術優勢、提供卓越的臨牀實用價值和具有重大市場機會的領域。欲瞭解更多信息,請訪問該公司網站:

We encourage our shareholders to visit our corporate social media accounts for updates:

我們鼓勵我們的股東訪問我們的企業社交媒體帳户以獲取最新消息:

About PRV-002
PRV-002 is a fully synthetic non-naturally occurring neurosteroid being developed for the treatment of mTBI (concussion). In preclinical studies, PRV-002 has demonstrated equivalent, if not superior, neuroprotective effects compared to related neurosteroids. Animal models of concussion demonstrated that PRV-002 reduces the behavioral pathology associated with brain injury symptoms such as memory impairment, anxiety, and motor/sensory performance. Additionally, PRV-002 is lipophilic and can easily cross the blood-brain barrier to rapidly eliminate swelling, oxidative stress and inflammation in the brain while restoring proper blood flow.

關於PRV-002
PRV-002是一種完全合成的非自然產生的神經類固醇,正在開發用於治療腦震盪。在臨牀前研究中,PRV-002已經證明瞭與相關神經類固醇相比,即使不是更好,也有同等的神經保護作用。腦震盪的動物模型表明,PRV-002可以減少與腦損傷症狀相關的行為病理,如記憶障礙、焦慮和運動/感覺表現。此外,PRV-002是親脂性的,可以很容易地穿過血腦屏障,在恢復正常血液流動的同時,迅速消除大腦中的腫脹、氧化應激和炎症。

About Nucleus Network

關於Nucleus網絡

Nucleus Network is the only multi-site Phase 1 clinical trials provider located in Australia and the USA. Nucleus Network provides high-quality, first-in-human and early-phase trials for biotechnology and pharmaceutical companies across the USA, Europe and Asia. Located within cutting-edge health precincts, their cost-effective, accelerated clinical development solutions are supported by advanced technology, clinical excellence, and research expertise.

Negus Network是位於澳大利亞和美國的唯一一家多站點一期臨牀試驗提供商。核心網絡公司為美國、歐洲和亞洲的生物技術和製藥公司提供高質量的首例人類試驗和早期試驗。位於尖端健康領域,他們的經濟高效、加速的臨牀開發解決方案得到了先進技術、卓越的臨牀和研究專業知識的支持。

Forward-Looking Statements
This news release may contain forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Such statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of various factors and uncertainties, including our ability to continue to raise needed funds, successfully complete the Phase I trial, our ability to successfully develop products, rapid changes in our markets, changes in demand for our future products, and legislative, regulatory, competitive developments and general economic conditions.

前瞻性陳述
本新聞稿可能包含1995年私人證券訴訟改革法中“安全港”條款所指的前瞻性陳述。此類陳述是基於我們目前的預期,僅代表截至本文發佈之日的情況。由於各種因素和不確定因素,我們的實際結果可能與任何前瞻性陳述中所表達的大不相同,這些不確定因素包括我們繼續籌集所需資金的能力,成功完成第一階段試驗的能力,我們成功開發產品的能力,我們市場的快速變化,對我們未來產品的需求變化,以及立法、法規、競爭發展和總體經濟狀況。

Inquiries:
Odyssey Health
info@odysseyhealthinc.com

查詢:
奧德賽健康
電子郵箱:Info@odyseyHealth Thinc.com


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