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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 提交研究新藥申請,對其 VELDONA 低劑量口服干擾素配方對輕度 COVID-19 症狀進行第二期試驗
Accesswire ·  2022/08/24 07:00

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

加利福尼亞州聖地牙哥/連接線/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.

$Ainos (AIMD.US)$(以下簡稱「Ainos」或「公司」) 是一家多元化醫療科技公司,專注於開發新型照護點測試、低劑量干擾素治療和合成 RNA 驅動預防藥物,今天宣佈已向美國食品藥物管理局提交了一項研究性新藥 (IND) 申請,以進行低劑量口服干擾素 (IFN-alpha®) 二期試驗。用於治療與 COVID-19 相關的輕度症狀。

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,公司的第二期試驗將涉及在台灣進行的多中心平行隨機研究,以評估 VELDONA® 在與 COVID-19 相關輕度症狀的受試者中的有效性。按照目前的計劃,人類受試者將接受每日口服劑量的 VELDONA® 或 5 天的護理標準(SoC),並將在 28 天的研究期內進行評估。

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 IFN 已證明免疫調節作用和干擾病毒複製的能力,可能是一種有效的抗病毒劑。「患者有嚴重和關鍵的 COVID-19 條件, 似乎受到在 I 型 IFN 響應損害的影響 (沒有 IFN-β 和低 IFN-阿爾法生產和活動).我們公司正在調查 I 型 IFN 受損是否可能與 COVID-19 病例中持續的高血病毒載量和炎症反應有關。」公司董事會主席、總裁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.

艾諾斯已經開發了其低劑量口服 IFN-α 配方 VELDONA®,以增強人類對疾病和感染的免疫反應。該公司先前的研究表明,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.

他說:「我們繼續根據我們先前對流感、普通傷風和流感的研究進行研究。鑑於到目前為止,我們對 VELDONA® 的結果充滿希望,我們樂觀地認為它可能在未來成為輕度 COVID-19 症狀的潛在治療方法。我們也期待擴大我們用於治療其他病毒感染的 VELDONA® 平台,這是我們長期策略的一部分,旨在增強和實現這種獨特化合物的價值。」

About Ainos, Inc.

關於艾諾斯公司

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. 總部位於加利福尼亞州聖地牙哥,是一家多元化的醫療科技公司,致力於開發創新醫療技術,用於點護理測試和安全和新穎的醫療治療,用於廣泛的疾病適應症。除了採用低劑量非注射干擾素的專有療法外,Ainos 還致力於開發包含醫療設備和消費性保健產品的全面醫療保健業務組合。Ainos 在優先考慮醫療器械商業化作為其多樣化策略的一部分的同時,還擴大了其產品組合,包括揮發性有機化合物(VOC)和 COVID-19 POCs。公司利用與揮發性有機化合物技術和 COVID-19 POCT 產品相關的專利,致力於加快其醫療器械管線的商品化,從 AIOS 品牌 COVID-19 POCT 產品候選產品開始。有關本公司的更多資訊,可在以下網址找到。

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.

本新聞稿載有《1995 年美國私人證券訴訟改革法案》安全港條款所指的「前瞻性陳述」。前瞻性陳述可以通過諸如「預測」,「相信」,「估計」,「期望」,「意圖」,「計劃」,「預測」,「項目」,「目標」,「未來」,「尋求」,「可能」,「策略」,「可能」,「可能」,「應」,「將」和類似的未來時期引用來標識。前瞻性陳述僅基於我們目前的信念,期望和假設。前瞻性陳述受到固有的不確定性、風險和難以預測的情況變化的影響,其中許多情況都不在我們控制範圍內。我們的實際結果可能與前瞻性陳述中指出的結果有很大差異。

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重要因素有很大差異,包括以下內容:本新聞稿中宣布的計劃藥物治療的生產成本和銷售潛力;美國食品藥物管理局(「FDA」)或其他規劃中藥物治療的監管機構的最終批准的影響;公司的現金損失有限公司(「公司」)的實現能力盈利能力; 公司行業中的激烈競爭和快速發展技術,這些技術可能超過其技術; 客戶對公司開發的產品和服務的需求; 競爭性或替代產品,技術和價格的影響; 公司生產其開發任何產品的能力; 一般的經濟條件和事件以及他們可能對公司及其潛在客戶產生的影響,包括但不限於其開發的任何產品; 一般的經濟條件和事件以及他們可能對公司及其潛在客戶產生的影響,包括但不限於 Covid-19 的融資能力。未來; 該世界衛生組織、食品和藥物管理局及其他政府部門頒布和實施法規的影響,其功能類似於本公司的營運和技術;第三方提起訴訟及其他索賠或由本公司各監管機構進行調查;公司有能力獲得其產品監管批准;以及我們成功管理上述項目涉及的風險。讀者還應審查我們截至 2021 年 12 月 31 日止年度的 10-K 表年度報告中列出的風險和不確定性,以及我們向美國證券交易委員會提交的其他報告。

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.

我們在本新聞稿中作出的任何前瞻性陳述,只會說明自該聲明作出的日期為止。我們沒有義務公開更新任何可能不時作出的前瞻性聲明,無論是由於新資訊、未來發展或其他原因而作出的。

Investor Relations Contact

投資者關係聯絡

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

ICR, 有限責任公司
楊羅賓
電話:1 646-224-6971
電郵地址:Ainos.IR@icrinc.com

SOURCE: Ainos, Inc.

來源: 艾诺斯公司

声明:本內容僅用作提供資訊及教育之目的,不構成對任何特定投資或投資策略的推薦或認可。 更多信息
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