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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 向美国食品药品管理局提交了研究性新药申请,要求对其 VELDONA 低剂量口服干扰素配方进行针对轻度 COVID-19 症状的 2 期试验
Accesswire ·  2022/08/24 07:00

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

加利福尼亚州圣地亚哥/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.

$Ainos (AIMD.US)$(“Ainos” 或 “公司”)是一家专注于开发新型即时检测、低剂量干扰素疗法和合成RNA驱动的预防药物的多元化医疗技术公司,今天宣布已向美国食品药品监督管理局提交了研究性新药(IND)申请,要求对其低剂量口服干扰素(IFN)-α配方VELDONA® 进行2期试验,用于治疗与 COVID-19 相关的轻微症状。

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.

如果获得批准,该公司的2期试验预计将涉及一项在台湾进行的多中心、平行、随机研究,以评估VELDONA® 对与 COVID-19 相关的轻度症状的受试者的疗效。按照目前的计划,人类受试者将接受为期5天的每日口服剂量的VELDONA® 或标准护理(SoC),并将在 28 天的研究期内接受评估。

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型干扰素已显示出免疫调节作用和干扰病毒复制的能力,可能是一种有效的抗病毒药物。“患有严重和危急 COVID-19 疾病的患者似乎受到 I 型干扰素反应受损(无干扰素β和干扰素α的产生和活性低)的影响。我们公司正在调查受损的I型IFN是否可能与 COVID-19 病例中持续的高血液病毒载量和炎症反应有关。” 该公司董事会主席、总裁兼首席执行官蔡春贤说。

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开发了其低剂量口服干扰素-α配方VELDONA®,以增强人类对疾病和感染的免疫反应。该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.

“我们继续在先前对流感、普通感冒和流感的研究基础上再接再厉。鉴于我们迄今为止使用VELDONA® 的令人鼓舞的结果,我们乐观地认为它将来它可能成为治疗轻度 COVID-19 症状的潜在方法。我们还期待扩展我们用于治疗其他病毒感染的VELDONA® 平台,这是我们提高和实现这种独特化合物价值的长期战略的一部分。” Ainos首席执行官蔡春贤说。

About Ainos, Inc.

关于 Ainos, Inc.

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. 总部位于加利福尼亚州圣地亚哥,是一家多元化的医疗技术公司,致力于开发创新的医疗技术,用于各种疾病适应症的即时检测以及安全和新颖的医疗治疗。除了使用低剂量不可注射干扰素的专有疗法外,Ainos还致力于开发包括医疗设备和消费保健产品在内的全面的医疗保健业务组合。在将医疗器械商业化作为其多元化战略一部分的优先事项的同时,Ainos还扩大了其产品组合,将挥发性有机化合物 (VOC) 和 COVID-19 POCT 包括在内。利用其与挥发性有机化合物技术和 COVID-19 POCT 产品相关的专利,该公司寻求加快其医疗器械产品线的商业化,首先是Ainos品牌的 COVID-19 POCT 候选产品。有关公司的更多信息,请访问。

Forward-Looking Statements

前瞻性陈述

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.

本新闻稿包含1995年《美国私人证券诉讼改革法》安全港条款所指的 “前瞻性陈述”。前瞻性陈述可以用 “预期”、“相信”、“估计”、“期望”、“打算”、“计划”、“预测”、“项目”、“目标”、“未来”、“寻求”、“可能”、“战略”、“可能”、“应该”、“将” 等词语以及与未来时期的类似提法来识别。前瞻性陈述仅基于我们当前的信念、期望和假设。前瞻性陈述受固有的不确定性、风险和情况变化的影响,这些不确定性、风险和情况变化难以预测,其中许多是我们无法控制的。我们的实际结果可能与前瞻性陈述中显示的结果存在重大差异。

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.

可能导致我们的实际业绩与前瞻性陈述中显示的结果存在重大差异的重要因素包括:本新闻稿中宣布的计划药物治疗的生产成本和销售潜力;美国食品药品监督管理局(“FDA”)或其他监管机构对计划药物治疗的最终批准的影响,包括紧急使用授权的可用性;公司的现金和亏损历史;公司的能力实现盈利能力;公司行业的激烈竞争和可能超过其技术的飞速发展的技术;客户对公司开发的产品和服务的需求;竞争或替代产品、技术和定价的影响;公司生产其开发的任何产品的能力;总体经济状况和事件及其可能对公司及其潜在客户产生的影响,包括但不限于Covid-19的影响;公司未来获得充足融资的能力;这个世界卫生组织、美国食品和药物管理局和其他职能与美国食品和药物管理局相似的政府机构颁布和实施法规对公司运营和技术的影响;第三方提起的诉讼和其他索赔或各种监管机构对公司运营的调查;公司获得监管部门批准的能力;以及我们在管理上述项目所涉及的风险方面的成功。读者还应查看我们截至2021年12月31日的10-K表年度报告以及我们向美国证券交易委员会提交的其他报告中列出的风险和不确定性。

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.

我们在本新闻稿中作出的任何前瞻性陈述仅代表截至该声明发表之日。我们没有义务公开更新可能不时作出的任何前瞻性陈述,无论是书面还是口头陈述,无论是由于新信息、未来发展还是其他原因。

Investor Relations Contact

投资者关系联系人

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

ICR, LLC
杨罗宾
电话:+1 646-224-6971
电子邮件:Ainos.IR@icrinc.com

SOURCE: Ainos, Inc.

来源: Ainos, Inc.

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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