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Ainos Submits Investigational New Drug Application to the U.S. FDA to Conduct Phase 2 Trial of Its VELDONA Low-dose Oral Interferon Formulation Against Mild COVID-19 Symptoms

Ainos Submits Investigational New Drug Application to the U.S. FDA to Conduct Phase 2 Trial of Its VELDONA Low-dose Oral Interferon Formulation Against Mild COVID-19 Symptoms

Ainos向美國FDA提交正在研究的新藥申請,以進行其VELDONA低劑量口服幹擾素配方治療輕度新冠肺炎症狀的第二階段試驗
Accesswire ·  2022/08/24 19:00

SAN DIEGO, CA / ACCESSWIRE / August 24, 2022 / 

加利福尼亞州聖迭戈/ACCESSWIRE/2022年8月24日/

$Ainos (AIMD.US)$ ("Ainos", or the "Company"), a diversified medtech company focused on the development of novel point-of-care testing, low-dose interferon therapeutics, and synthetic RNA-driven preventative medicine, today announced it has submitted an Investigational New Drug (IND) application to the U.S. Food and Drug Administration for conducting a Phase 2 trial of its low-dose oral interferon (IFN)-alpha formulation, VELDONA®, for treatment of mild symptoms related to COVID-19.

$Ainos (AIMD.US)$致力於開發新型護理點檢測、低劑量幹擾素療法和合成核糖核酸驅動的預防藥物的多元化醫療科技公司Ainos今天宣佈,已向美國食品和藥物管理局提交了一份研究性新藥申請,將對其低劑量口服幹擾素-α製劑VELDONA®進行第二階段試驗,用於治療與新冠肺炎相關的輕微症狀。

If approved, the Company's Phase 2 trial is expected to involve a multicenter, parallel, randomized study conducted in Taiwan to evaluate the efficacy of VELDONA® in subjects with mild symptoms related to COVID-19. As currently planned, human subjects will receive either a daily oral dose of VELDONA® or a standard of care (SoC) for 5 days and will be evaluated throughout a 28-day study period.

如果獲得批准,該公司的第二階段試驗預計將涉及在臺灣進行的一項多中心、平行、隨機研究,以評估VELDONA®對出現與新冠肺炎有關的輕微症狀的受試者的療效。按照目前的計劃,人類受試者將接受為期5天的每日口服劑量的VELDONA®或標準護理(SOC),並將在整個28天的研究期間接受評估。

Type I IFN, which has demonstrated immunomodulating effects and an ability to interfere with viral replication, may be an effective antiviral agent. "Patients with severe and critical COVID-19 conditions, seem to be affected by an impairment in type I IFN response (no IFN-beta and low IFN-alpha production and activity). Our Company is investigating whether impaired type I IFN could be related to persistent high blood viral loads and inflammatory responses in COVID-19 cases." stated Chun-Hsien Tsai, the Company's Chairman of the Board, President and CEO.

I型幹擾素具有免疫調節作用和幹擾病毒複製的能力,可能是一種有效的抗病毒藥物。嚴重和危重的新冠肺炎患者似乎受到I型幹擾素反應受損的影響(沒有幹擾素-β和低幹擾素-α的產生和活性)。我們公司正在調查新冠肺炎患者中I型幹擾素受損是否與持續的高病毒載量和炎症反應有關。公司董事局主席兼首席執行官蔡俊賢表示。

Ainos has developed its low-dose oral IFN-alpha formulation VELDONA® to boost the human immune response against disease and infection. The Company's previous studies have demonstrated that VELDONA could inhibit respiratory virus infection, including influenza A.

Ainos已經開發出低劑量口服幹擾素-α配方VELDONA®,以增強人類對疾病和感染的免疫反應。該公司以前的研究表明,VELDONA可以抑制呼吸道病毒感染,包括甲型流感。

"We continue to build on our prior studies on influenza, the common cold and flu. Given our promising results with VELDONA® to date, we are optimistic that it may become a potential treatment for mild COVID-19 symptoms in the future. We also look forward to expanding our VELDONA® platform for treatment of other viral infections, as a component of our long-term strategy to enhance and realize the value of this unique compound." stated Ainos' CEO Chun-Hsien Tsai.

我們繼續在我們以前對流感、普通感冒和流感的研究的基礎上再接再厲。鑑於我們對VELDONA®迄今取得的令人振奮的結果,我們樂觀地認為,它可能在未來成為治療輕微新冠肺炎症狀的潛在療法。我們還期待着擴大我們的VELDONA®平臺,用於治療其他病毒感染,作為我們加強和實現這種獨特化合物價值的長期戰略的一部分。Ainos的首席執行官蔡俊賢説。

About Ainos, Inc.

關於Ainos公司

Headquartered in San Diego, California, Ainos, Inc. is a diversified medtech company engaged in developing innovative medical technologies for point-of-care testing and safe and novel medical treatment for a broad range of disease indications. In addition to its proprietary therapeutics using low-dose non-injectable interferon, Ainos is committed to developing a comprehensive healthcare business portfolio encompassing medical devices and consumer healthcare products. While prioritizing the commercialization of medical devices as part of its diversification strategy, Ainos has also expanded its product portfolio to include Volatile Organic Compounds (VOC) and COVID-19 POCTs. Leveraging its patents related to VOC technologies and COVID-19 POCT products, the Company seeks to expedite the commercialization of its medical device pipeline, beginning with Ainos-branded COVID-19 POCT product candidates. More information about the Company may be found at .

Ainos,Inc.總部設在加利福尼亞州聖地亞哥,是一家多元化的醫療科技公司,致力於開發創新的醫療技術,用於護理點檢測和針對各種疾病適應症的安全和新穎的醫療治療。除了使用低劑量非注射幹擾素的專利療法外,Ainos還致力於開發涵蓋醫療設備和消費者保健產品的全面醫療保健業務組合。在將醫療器械商業化作為其多元化戰略的一部分作為優先事項的同時,Ainos還擴大了其產品組合,包括揮發性有機化合物(VOC)和新冠肺炎POCT。利用其與VOC技術和新冠肺炎POCT產品相關的專利,該公司尋求加快其醫療器械生產線的商業化進程,首先是Ainos品牌的新冠肺炎POCT候選產品。有關該公司的更多信息,請訪問。

Forward-Looking Statements

前瞻性陳述

This press release contains 'forward-looking statements' within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as "anticipate," "believe," "estimate," "expect," "intend," "plan," "predict," "project," 'target," "future," "seek," "likely," "strategy," "may," "should," "will," and similar references to future periods. Forward-looking statements are based only on our current beliefs, expectations, and assumptions. Forward-looking statements are subject to inherent uncertainties, risks, and changes in circumstances that are difficult to predict and many of which are outside of our control. Our actual results may differ materially from those indicated in the forward-looking statements.

本新聞稿包含符合1995年美國私人證券訴訟改革法安全港條款的“前瞻性陳述”。前瞻性陳述可以通過諸如“預期”、“相信”、“估計”、“預期”、“打算”、“計劃”、“預測”、“項目”、“目標”、“未來”、“尋求”、“可能”、“戰略”、“可能”、“應該”、“將會”以及對未來時期的類似提法來識別。前瞻性陳述僅基於我們當前的信念、預期和假設。前瞻性陳述會受到固有的不確定性、風險和環境變化的影響,這些不確定性、風險和變化很難預測,其中許多是我們無法控制的。我們的實際結果可能與前瞻性陳述中指出的大不相同。

Important factors that could cause our actual results to differ materially from those indicated in the forward-looking statements include, among others, the following: the cost of production and sales potential of the planned drug treatments announced in this press release; the impact of final approvals from the U.S. Food and Drug Administration (the "FDA") or other regulatory bodies for the planned drug treatments including the availability of emergency use authorization; the Company's limited cash and history of losses; the Company's ability to achieve profitability; intense competition and rapidly advancing technology in the Company's industry that may outpace its technology; customer demand for the products and services the Company develops; the impact of competitive or alternative products, technologies and pricing; the Company's ability to manufacture any products it develops; general economic conditions and events and the impact they may have on the Company and its potential customers, including but not limited to the impact of Covid-19; the Company's ability to obtain adequate financing in the future; the impact of promulgation and implementation of regulations by the World Health Organization, the FDA and by other governmental authorities with functions similar to those of the FDA on the Company's operations and technologies; lawsuits and other claims by third parties or investigations by various regulatory agencies governing the Company's operations; the Company's ability to secure regulatory approvals for its products; and our success in managing the risks involved in the foregoing items. Readers should also review the risks and uncertainties listed in our Annual Report on Form 10-K for the year ended December 31, 2021 and other reports we file with the U.S. Securities and Exchange Commission.

可能導致我們的實際結果與前瞻性陳述中顯示的結果大不相同的重要因素包括但不限於:本新聞稿中宣佈的計劃藥物治療的生產成本和銷售潛力;美國食品和藥物管理局(FDA)或其他監管機構對計劃藥物治療的最終批准的影響,包括緊急使用授權的可用性;公司有限的現金和歷史虧損;公司實現盈利的能力;公司行業的激烈競爭和快速進步的技術可能超過其技術;客户對公司開發的產品和服務的需求;競爭性或替代產品、技術和定價的影響;公司生產其開發的任何產品的能力;總體經濟狀況和事件及其可能對公司及其潛在客户造成的影響,包括但不限於“新冠肺炎”的影響;公司未來獲得充足資金的能力;世界衞生組織、食品和藥物管理局以及其他職能類似於食品和藥物管理局的政府機構頒佈和實施法規對公司業務和技術的影響;第三方的訴訟和其他索賠或管理公司運營的各種監管機構的調查;公司確保其產品獲得監管部門批准的能力;以及我們成功地管理上述項目中涉及的風險。讀者還應查閲我們截至2021年12月31日的Form 10-K年度報告以及我們提交給美國證券交易委員會的其他報告中列出的風險和不確定性。

Any forward-looking statement made by us in this press release speaks only as of the date on which such statement is made. We undertake no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.

我們在本新聞稿中所作的任何前瞻性聲明僅限於該聲明發表之日。我們沒有義務公開更新任何可能不時作出的前瞻性陳述,無論是書面的還是口頭的,無論是新信息、未來發展還是其他情況。

Investor Relations Contact

投資者關係聯繫人

ICR, LLC
Robin Yang
Tel: +1 646-224-6971
Email: Ainos.IR@icrinc.com

ICR,LLC
楊彥宏
電話:+1646-224-6971
電子郵件:Ainos.IR@icrinc.com

SOURCE: Ainos, Inc.

資料來源:Ainos公司

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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