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Ainos Pursues Licensing Partners To Accelerate Five Candidates Of Its Low-dose Oral Interferon Formulation VELDONA To Phase 3 Trials And Commercialization

Ainos Pursues Licensing Partners To Accelerate Five Candidates Of Its Low-dose Oral Interferon Formulation VELDONA To Phase 3 Trials And Commercialization

Ainos尋求授權合作伙伴加快其低劑量口服幹擾素配方VELDONA的五個候選產品進入第三階段試驗和商業化
Benzinga Real-time News ·  2022/10/31 07:11

Ainos, Inc. (NASDAQ:AIMD)(NASDAQ:AIMDW) ("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 that it is pursuing out-licensing opportunities for five new drug candidates for its low-dose oral interferon-alpha ("IFNα") formulation, VELDONA. Ainos has completed Phase 2 trials for the five new drug candidates and will work with potential partners to accelerate the candidates to Phase 3 trials and eventual commercialization of VELDONA. 

愛諾斯公司(納斯達克代碼:AIMD)(納斯達克代碼:AIMDW)(以下簡稱“公司”)是一家多元化的醫療科技公司,專注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。該公司今天宣佈,它正在為其低劑量口服幹擾素-α(“α”)配方VELDONA的五種新藥候選藥物尋求許可外機會。Ainos已經完成了5種候選新藥的第二階段試驗,並將與潛在合作伙伴合作,加快候選藥物進入第三階段試驗並最終實現VELDONA的商業化。

The following five indications have completed Phase 2 trials. Ainos aims to enter out-licensing agreements to advance VELDONA to Phase 3 trials and commercialization.

以下五種適應症已完成第二階段試驗。Ainos的目標是達成外部許可協議,將VELDONA推進到第三階段試驗和商業化。

  • Sjögren's syndrome (US IND No. 5700)

  • Aphthous Stomatitis (US IND No. 5126)

  • Chemotherapy-induced Stomatitis (US IND No. 5587)

  • Influenza (Australian ACTRNACTRN12609000976280)

  • Common Cold (US IND No. 5244)

  • SJÖGren‘s綜合徵(美國IND No.5700)

  • 口腔炎(美國IND NO.5126)

  • 化療所致口腔炎(美國IND NO.5587)

  • 流感(澳大利亞ACTRNACTRN12609000976280)

  • 普通感冒(美國IND NO.5244)

The Company's product is delivered into the oral cavity as a lozenge in low (nanogram) doses. Human studies have shown that IFNα given orally is effective against viral and autoimmune diseases, without the side effects associated with high-dose injections of IFNα. Ainos has cumulatively spent nearly $40 million on developments related to the oral use of IFNα (VELDONA formulation), not including the expected expenses on clinical trials and manufacturing VELDONA. To date, 68 clinical trials have been conducted with low-dose oral IFNα. Sixty-three studies were Phase 2 trials, and three Phase 1 and two Phase 3 studies have also been conducted. Nearly 6,000 patients with one of 16 different disease indications and/or healthy volunteers participated in these trials, including a total of 4,600 subjects exposed to IFNα at a dose level ranging from three to 2,000 international units given daily for up to five years. The safety of orally administered IFNα has been consistently demonstrated in these trials.

該公司的產品以低(納克)劑量的含片形式進入口腔。人體研究表明,口服幹擾素α對病毒和自身免疫性疾病有效,沒有與大劑量注射幹擾素α相關的副作用。Ainos已累計花費近4,000萬美元用於與口服幹擾素α(VELDONA製劑)相關的開發,這還不包括臨牀試驗和製造VELDONA的預期費用。到目前為止,低劑量口服幹擾素α已經進行了68項臨牀試驗。63項研究是第二階段試驗,也進行了三項第一階段研究和兩項第三階段研究。近6,000名具有16種不同疾病指徵之一的患者和/或健康志願者參加了這些試驗,其中包括總共4,600名受試者,他們每天給予幹擾素α的劑量從3到2,000國際單位不等,最長持續5年。口服幹擾素α的安全性在這些試驗中得到了一致的證明。

Interferons are proteins made by host cells in response to the presence of pathogens such as viruses, bacteria, parasites, or tumor cells. They allow for communication between cells to trigger the protective defenses of the immune system that eradicate pathogens or tumors. Of the nine different families of human interferon that have been identified, interferon-alpha is the most widely studied. The US FDA has approved the use of IFNα in mega doses given by injection for treating a number of cancers, as well as Hepatitis B and C.

幹擾素是宿主細胞在病毒、細菌、寄生蟲或腫瘤細胞等病原體存在時產生的蛋白質。它們允許細胞之間的通信,以觸發免疫系統的保護性防禦,從而根除病原體或腫瘤。在已經確定的九種不同的人類幹擾素家族中,幹擾素-α是研究最廣泛的。美國食品和藥物管理局已經批准大劑量注射幹擾素α用於治療一些癌症以及乙肝和丙型肝炎。

Ainos's low-dose oral VELDONA formulation is designed to enhance autoimmunity to resist virus damage, potentially reducing side effects and risks caused by high-dose interferon and other small molecule drugs.

Ainos的低劑量口服VELDONA配方旨在增強自身免疫力,以抵抗病毒損害,潛在地減少大劑量幹擾素和其他小分子藥物造成的副作用和風險。

Positive effects of oral VELDONA treatment have been noted across a wide range of disease indications, including:

口服VELDONA治療在一系列疾病適應症中都有積極的效果,包括:

  • In Sjögren's syndrome (SS) (US IND No. 5700), after 48 weeks of treatment the clinical results showed increased unstimulated whole saliva and improvement in mouth dryness and seven other SS symptoms.

  • In Aphthous Stomatitis (US IND No. 5126), the clinical results showed clearance of existing lesions and reduced severity of new lesions.

  • In Chemotherapy-induced Stomatitis (US IND No. 5587), the clinical results showed reduced severity during repeat chemotherapy.

  • In Influenza (Australian ACTRNACTRN12609000976280), the clinical results showed reduced incidence of moderate to severe symptoms; remission of sore throat, fever and head congestion; and significantly reduced influenza-like illness rate in three subgroups: 50 year and older, those vaccinated against seasonal flu, and males.

  • In Common Cold (US IND No. 5244), the clinical results showed immediate reduction of malaise and sore throat after 6 hours from initial treatment.

  • 在SJÖGren‘s綜合徵(SS)(美國IND5700號)中,治療48周後,臨牀結果顯示非刺激性全唾液增加,口腔乾燥和其他7種SS症狀得到改善。

  • 在口腔炎(US IND NO.5126)中,臨牀結果顯示現有病變清除,新病變嚴重程度減輕。

  • 在化療引起的口腔炎(US IND No.5587)中,臨牀結果顯示在重複化療期間病情有所減輕。

  • 在流感(澳大利亞ACTRNACTRN12609000976280)中,臨牀結果顯示中到重度症狀的發生率降低,喉嚨痛、發燒和頭部充血緩解,並顯著降低了三個亞組的流感樣疾病發生率:50歲及以上、接種季節性流感疫苗的人和男性。

  • 在普通感冒(美國IND NO.5244)中,臨牀結果顯示,從最初治療起6小時後,不適和喉嚨痛立即減輕。

Chun-Hsien Tsai, Ainos' Chairman of the Board, President, and Chief Executive Officer, commented, "Low-dose oral interferon-alpha treatments have shown a promising array of potential applications through Phase 2 clinical trials. We have recently carried out studies that demonstrate VELDONA's effectiveness in protecting against symptoms associated with COVID-19 and prevention and treatment of influenza. By exploring out-licensing opportunities for our five VELDONA new drug candidates, we plan to accelerate commercialization of our VELDONA technology as rapidly as possible."

愛諾仕董事局主席兼首席執行官蔡俊賢表示:“低劑量口服幹擾素-α療法在第二階段臨牀試驗中顯示出了一系列很有前途的潛在應用。我們最近進行的研究表明,VELDONA在預防新冠肺炎相關症狀和預防和治療流感方面是有效的。通過為我們的五種候選新藥探索授權外機會,我們計劃儘快加快VELDONA技術的商業化進程。”

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