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Innovation Pharmaceuticals Provides Update on U.S. Patent Applications Covering Use of Brilacidin in Inflammatory Bowel Diseases, Coronaviruses and Fungal Diseases

Innovation Pharmaceuticals Provides Update on U.S. Patent Applications Covering Use of Brilacidin in Inflammatory Bowel Diseases, Coronaviruses and Fungal Diseases

Innovation Pharmicals提供有關Brilacidin在炎症性腸病、冠狀病毒和真菌疾病中的使用的美國專利申請的最新情況
GlobeNewswire ·  2023/06/21 20:00

WAKEFIELD, MA, June 21, 2023 (GLOBE NEWSWIRE) -- via NewMediaWire – Innovation Pharmaceuticals (OTCQB:IPIX) ("the Company"), a clinical stage biopharmaceutical company, today announced the United States Patent and Trade Office (USPTO), on June 6, 2023, granted a patent, "Host Defense Protein (HDP) Mimetics for Prophylaxis and/or Treatment of Inflammatory Diseases of the Gastrointestinal Tract," and also recently issued a Notice of Allowance for the patent application, "Arylamide Compounds For Treatment Of Viral Infections."

亞洲網馬薩諸塞州韋克菲爾德2023年6月21日電臨床階段生物製藥公司Via NewMediaWire-Innovation PharmPharmticals(OTCQB:IPIX)(“本公司”)今天宣佈,美國專利和貿易局(USPTO)於2023年6月6日授予“用於預防和/或治療胃腸道炎症性疾病的宿主防禦蛋白(HDP)類比物”專利,並於最近發佈了一項專利申請許可通知,該專利申請名為“用於治療病毒感染的芳酰胺化合物”。

These allowed patents, which encompass Brilacidin protections through 2036 and 2041, respectively, further strengthen Brilacidin intellectual property rights previously granted in the U.S. and other regions. Brilacidin is a Host Defense Protein-mimetic drug candidate with broad-spectrum immunomodulatory and antimicrobial properties.

這些允許的專利分別涵蓋到2036年和2041年的Brilacidin保護,進一步加強了Brilacidin之前在美國和其他地區授予的知識產權。Brilacidin是一種類似宿主防禦蛋白的候選藥物,具有廣譜的免疫調節和抗菌特性。

Related to the claims of these newly allowed patents, Brilacidin has been tested in Ulcerative Proctitis/Ulcerative Proctosigmoiditis (UP/UPS) (by rectal enema administration), where most patients achieved clinical remission, with further progress made in the development of an oral Brilacidin formulation for treatment of Ulcerative Colitis and Crohn's Disease. The Company out-licensed Brilacidin in UP/UPS to Alfasigma S.p.A. Brilacidin has also been evaluated in Phase 2 testing in moderate-to-severe hospitalized cases of COVID-19 (by intravenous delivery), with beneficial treatment effects observed in patient subgroups. Biomarker-based trial design (enrollment tied to specific subgroups) has been highlighted by Biomedical Advanced Research and Development Authority (BARDA) scientists as a critical step to increase the likelihood of achieving clinical efficacy of investigational drugs in COVID-19 and Acute Lung Injury (ALI)/Acute Respiratory Distress Syndrome (ARDS).

與這些新批准的專利的權利要求有關,Brilacidin已經在潰瘍性直腸炎/潰瘍性前乙狀結腸炎(UP/UPS)(通過直腸灌腸給藥)中進行了測試,大多數患者在臨床上獲得了緩解,用於治療潰瘍性結腸炎和克羅恩病的口服Brilacidin配方的開發取得了進一步的進展。該公司將Brilacidin在UP/UPS中的授權授予Alfasigma S.p.A.。Brilacidin還在新冠肺炎中至重度住院病例(通過靜脈注射)的第二階段測試中進行了評估,並在患者分組中觀察到了有益的治療效果。生物醫學高級研究與發展局(BARDA)的科學家強調,基於生物標記物的試驗設計(登記與特定亞組相關)是增加研究藥物在新冠肺炎和急性肺損傷(Ali)/急性呼吸窘迫綜合徵(ARDS)取得臨床療效的可能性的關鍵一步。

A separate patent application has been submitted to the USPTO for use of Brilacidin in fungal diseases. Encouraging Brilacidin pre-clinical results (in vitro and in vivo) against multiple fungal infections have been achieved, as recently published in an article in Nature Communications, and based on in vitro screening studies conducted by independent researchers. Additional in vivo testing in efficacy models against two hard-to-treat fungal pathogens is scheduled for 3Q2023.

另一項專利申請已經提交給美國專利商標局,申請將Brilacidin用於真菌疾病。令人鼓舞的Brilacidin臨床前結果(體外和體內)對抗多種真菌感染已經取得了成果,最近發表在自然通訊,並基於體外培養篩選由獨立研究人員進行的研究。其他內容體內針對兩種難以治療的真菌病原體的療效模型測試定於2023年第三季度進行。

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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)是一家臨床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進行臨床前研究和臨床試驗以及在美國和其他司法管轄區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床前或臨床測試,或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;公司未來需要和可獲得的大量資本為其運營和研發提供資金,包括根據證券購買協定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床前或臨床測試,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檔案中。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資訊,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,除非適用的法律或法規另有要求,否則這些修訂可能反映本新聞稿發佈後的事件或情況,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


譯文內容由第三人軟體翻譯。


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