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Innovation Pharmaceuticals Announces NIH/NIAID-Affiliated Researchers to Evaluate Brilacidin's Treatment Potential Against Monkeypox

Innovation Pharmaceuticals Announces NIH/NIAID-Affiliated Researchers to Evaluate Brilacidin's Treatment Potential Against Monkeypox

創新制藥公司宣佈NIH/NIAID附屬研究人員評估Brilacidin治療猴痘的潛力
Accesswire ·  2022/08/05 21:35

WAKEFIELD, MA / ACCESSWIRE / August 5, 2022 / Innovation Pharmaceuticals (OTCQB:IPIX) ("the Company"), a clinical stage biopharmaceutical company, today announced that Brilacidin, the Company's defensin-mimetic drug candidate exhibiting broad-spectrum antiviral properties, is to be evaluated for its treatment potential against the monkeypox virus.

馬薩諸塞州韋克菲爾德2022年8月5日亞洲網加利福尼亞州聖何塞10月24日電臨牀階段生物製藥公司創新制藥公司(場外交易市場代碼:IPIX)(以下簡稱“公司”)今天宣佈,將對該公司具有廣譜抗病毒特性的擬防禦素候選藥物Brilacidin進行治療潛力評估。

To establish potential proof-of-concept, in vitro testing initially will be conducted in orthopoxviruses1 (poxviruses) related to monkeypox -- such as vaccinia and cowpox -- through a collaboration with National Institutes of Health (NIH)/National Institute of Allergy and Infectious Diseases (NIAID) scientists. Testing in poxviruses builds on earlier NIH/NIAID-affiliated research of Brilacidin in other acutely infectious virus families, including coronaviruses, alphaviruses, flaviviruses, and filoviruses, with a corresponding scientific paper being prepared for publication.

為了建立潛在的概念驗證,體外培養最初的檢測將在正痘病毒中進行1通過與國家衞生研究院(NIH)/國家過敏和傳染病研究所(NIAID)的科學家合作,開發了與猴痘有關的(痘病毒)--如牛痘和牛痘。痘病毒測試建立在NIH/NIAID早期對Brilacidin在其他急性傳染性病毒家族中的研究基礎上,包括冠狀病毒、甲型病毒、黃病毒和絲狀病毒,正在準備發表相應的科學論文。

Given Brilacidin has exhibited antiviral activity in multiple virus families, the Company is excited that Brilacidin will be tested in poxviruses. Academic literature supports Brilacidin's potential in poxviruses. For example, LL-37 and CRAMP, types of natural antimicrobial peptides with similar properties to those of Brilacidin but without the advantages of synthetic design, have been shown in vitro and in vivo to exert antiviral activity against the poxvirus vaccinia.2

鑑於Brilacidin已經在多個病毒家族中表現出抗病毒活性,該公司對Brilacidin將在痘病毒中進行測試感到興奮。學術文獻支持Brilacidin在痘病毒中的潛力。例如,已經展示了與Brilacidin性質相似但沒有合成設計優勢的天然抗菌肽--LL-37和CRAMP體外培養體內對痘病毒牛痘病毒施加抗病毒活性。2

"On the heels of the COVID-19 pandemic, which shows few signs of ending, the world is facing another viral outbreak in monkeypox," said Leo Ehrlich, Chief Executive Officer at Innovation Pharmaceuticals. "Unfortunately, there are no approved or authorized treatments in the U.S. for monkeypox, with, for the most part, only one drug -- TPOXX™ -- made available to clinicians under compassionate use requests. TPOXX™ was approved by the FDA in 2018 for the treatment of smallpox based on in vivo studies in related poxviruses. Should Brilacidin data in poxviruses be positive, we plan to take aggressive steps to pursue an abbreviated FDA pathway in a bid to provide an alternative treatment to help combat monkeypox."

創新制藥公司首席執行官利奧·埃爾利希表示:“新冠肺炎疫情幾乎沒有結束的跡象,緊隨其後,世界正面臨另一場猴痘病毒疫情。”不幸的是,美國還沒有批准或授權治療猴痘的藥物,大多數情況下,只有一種藥物--TPOXX™--可供臨牀醫生根據同情使用請求提供。TPOXX™於2018年被美國食品和藥物管理局批准用於治療天花,其基礎是體內對相關痘病毒的研究。如果痘病毒中的Brilacidin數據呈陽性,我們計劃採取積極措施,尋求FDA的簡化途徑,以提供一種幫助抗擊猴痘的替代治療方法。“

About Monkeypox3,4,5
Monkeypox is a contagious virus characterized by painful skin lesions and rashes and typically spreads through close physical contact. Symptoms usually start within 3 weeks of exposure to the virus, with the illness lasting 2 to 4 weeks. According to the World Health Organization (WHO) Emergency Dashboard, over 26,500 monkeypox cases have been reported in 92 countries. The Centers for Disease Control and Prevention (CDC) has indicated between 1.6 and 1.7 million people in the U.S. are at highest risk of monkeypox infection. The WHO has declared the global monkeypox outbreak a Public Health Emergency of International Concern, a designation reserved for only the most serious viral outbreaks, such as COVID-19, Zika and Ebola. The U.S. Department of Health and Human Services has also declared monkeypox a national public health emergency.

關於猴痘3,4,5
猴痘是一種傳染性病毒,以疼痛的皮膚皮損和皮疹為特徵,通常通過密切的身體接觸傳播。症狀通常在接觸病毒後3周內開始出現,病情持續2至4周。根據世界衞生組織(WHO)緊急儀表盤的數據,92個國家報告了超過26,500例猴痘病例。美國疾病控制和預防中心(CDC)表示,美國有160萬至170萬人感染猴痘的風險最高。世界衞生組織宣佈此次全球猴痘疫情為國際關注的突發公共衞生事件,這個名稱只適用於最嚴重的病毒爆發,如新冠肺炎、寨卡病毒和埃博拉病毒。美國衞生與公眾服務部也宣佈猴痘為全國突發公共衞生事件。

In the U.S., only two vaccines may be used for prevention of monkeypox (JYNNEOS™ and ACAM2000™) and there are no drugs yet approved or authorized for treatment of monkeypox. The antiviral tecovirimat (TPOXX™), approved in 2018 for treatment of smallpox under the FDA's Animal Rule (approval was granted based on well-controlled animal studies), is available for clinical use against monkeypox, via oral or IV delivery, but only under Expanded Access ("compassionate use") protocols. TPOXX™ is made available to clinicians in the U.S. through the Strategic National Stockpile (SNS), a national repository of antibiotics, antivirals, vaccines, antidotes, antitoxins, as well as other critical medical supplies, that can be readily accessed during disease outbreaks.

在美國,只有兩種疫苗可用於預防猴痘(JYNNEOS™和ACAM2000™),目前還沒有批准或授權用於治療猴痘的藥物。抗病毒藥物Tecovirimat(TPOXX™)於2018年根據FDA的動物規則(批准是基於受控的動物研究)被批准用於治療天花,可通過口服或靜脈注射用於臨牀治療猴痘,但必須根據擴大獲得(“同情使用”)協議。TPOXX™通過國家戰略儲備(SNS)提供給美國的臨牀醫生,國家戰略儲備是一個全國性的抗生素、抗病毒藥物、疫苗、解毒劑、抗毒素以及其他關鍵醫療用品的儲存庫,在疾病暴發期間可以很容易地獲得這些用品。

1 Orthopoxviruses Pathogenic for Humans | SpringerLink
2 Selective Killing of Vaccinia Virus by LL-37: Implications for Eczema Vaccinatum | The Journal of Immunology (jimmunol.org)
3 Monkeypox | Poxvirus | CDC
4 Monkeypox Outbreak 2022 - Global (who.int)
5 Tecovirimat and the Treatment of Monkeypox - Past, Present, and Future Considerations | NEJM

1人類致病的正痘病毒|SpringerLink
2IL-37選擇性殺滅痘苗病毒:對濕疹的影響|免疫學雜誌(jImmunol.org)
3 猴痘|痘病毒|疾控中心
4 2022年猴痘暴發-全球(wh.int)
5 Tecovirimat和猴痘的治療--過去、現在和未來的考慮

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About Innovation Pharmaceuticals
Innovation Pharmaceuticals Inc. (IPIX) is a clinical stage biopharmaceutical company developing a portfolio of innovative therapies addressing multiple areas of unmet medical need, including inflammatory diseases, cancer, and infectious diseases. The Company is also active in evaluating other potential investment opportunities that can add value and diversify its portfolio.

關於創新制藥公司
創新制藥公司(IPIX)是一家臨牀階段的生物製藥公司,開發一系列創新療法,以解決多種未得到滿足的醫療需求領域,包括炎症性疾病、癌症和傳染病。該公司還積極評估其他潛在的投資機會,以增加價值並使其投資組合多樣化。

Forward-Looking Statements: This press release contains forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995 including, without limitation, statements concerning future product development plans, including with respect to specific indications; statements regarding the therapeutic potential and capabilities of the StingRay System; future regulatory developments; and any other statements which are other than statements of historical fact. These statements involve risks, uncertainties and assumptions that could cause actual results and experience to differ materially from anticipated results and expectations expressed in these forward-looking statements. The Company has in some cases identified forward-looking statements by using words such as "anticipates," "believes," "hopes," "estimates," "looks," "expects," "plans," "intends," "goal," "potential," "may," "suggest," and similar expressions. Among other factors that could cause actual results to differ materially from those expressed in forward-looking statements are risks related to conducting pre-clinical studies and clinical trials and seeking regulatory and licensing approvals in the United States and other jurisdictions, including without limitation that compounds and devices may not successfully complete pre-clinical or clinical testing, or be granted regulatory approval to be sold and marketed in the United States or elsewhere; prior test results may not be replicated in future studies and trials; the Company's need for, and the availability of, substantial capital in the future to fund its operations and research and development, including the amount and timing of the sale of shares of common stock under securities purchase agreements; and the Company's licensee(s) may not successfully complete pre-clinical or clinical testing and the Company will not receive milestone payments. A more complete description of these and other risk factors is included in the Company's filings with the Securities and Exchange Commission. Many of these risks, uncertainties and assumptions are beyond the Company's ability to control or predict. You should not place undue reliance on any forward-looking statements. The forward-looking statements speak only as of the information currently available to the Company on the date they are made, and the Company undertakes no obligation to release publicly the results of any revisions to any such forward-looking statements that may be made to reflect events or circumstances after the date of this press release or to reflect the occurrence of unanticipated events, except as required by applicable law or regulation.

前瞻性陳述:本新聞稿包含根據1995年《私人證券訴訟改革法》的安全港條款作出的前瞻性陳述,包括但不限於有關未來產品開發計劃的陳述,包括有關特定適應症的陳述;有關黃貂魚系統治療潛力和能力的陳述;未來監管發展;以及除歷史事實陳述之外的任何其他陳述。這些陳述涉及風險、不確定性和假設,可能導致實際結果和經驗與這些前瞻性陳述中表達的預期結果和預期大不相同。在某些情況下,公司通過使用諸如“預期”、“相信”、“希望”、“估計”、“展望”、“預期”、“計劃”、“打算”、“目標”、“潛在”、“可能”、“建議”以及類似的表達方式來識別前瞻性陳述。可能導致實際結果與前瞻性陳述中表述的結果大不相同的其他因素包括,與在美國和其他司法管轄區進行臨牀前研究和臨牀試驗以及尋求監管和許可批准有關的風險,包括但不限於化合物和設備可能無法成功完成臨牀前或臨牀測試,或未獲得在美國或其他地方銷售和銷售的監管批准;以前的測試結果可能不會在未來的研究和試驗中複製;公司未來需要和獲得大量資本來資助其運營和研發, 包括根據證券購買協議出售普通股的金額和時間;公司的被許可人可能無法成功完成臨牀前或臨牀測試,公司將不會收到里程碑式的付款。關於這些和其他風險因素的更完整的描述包括在該公司提交給證券交易委員會的文件中。其中許多風險、不確定性和假設超出了公司的控制或預測能力。您不應過度依賴任何前瞻性陳述。前瞻性陳述僅代表公司在發佈之日目前掌握的信息,公司沒有義務公開發布對任何此類前瞻性陳述的任何修訂結果,除非適用法律或法規要求,否則這些修訂可能反映本新聞稿發佈之日之後的事件或情況,或反映意外事件的發生。

INVESTOR AND MEDIA CONTACTS
Innovation Pharmaceuticals Inc.
Leo Ehrlich
info@ipharminc.com

投資者和媒體聯繫
創新制藥公司。
利奧·埃爾利希
郵箱:Info@ipharminc.com

SOURCE: Innovation Pharmaceuticals Inc.

資料來源:創新制藥公司。


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