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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 08:00

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."

馬薩諸塞州韋克菲爾德,2023年6月21日(GLOBE NEWSWIRE)——通過NewMediaWire——臨床階段的生物製藥公司創新制藥公司(OTCQB: IPIX)(“公司”)今天宣佈,美國專利貿易局(USPTO)於2023年6月6日授予了一項專利,即 “用於預防和/或治療宿主防禦蛋白(HDP)模仿劑胃腸道炎性疾病”,最近還發布了允許申請專利 “用於治療病毒感染的芳酰胺化合物” 的通知。

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包括到2036年和2041年對Brilacidin的保護,進一步加強了先前在美國和其他地區授予的Brilacidin知識產權。Brilacidin 是一種模仿宿主防禦蛋白的候選藥物,具有廣譜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).

與這些新允許的專利的主張有關,Brilacidin已在潰瘍性直腸炎/潰瘍性直腸乙狀結腸炎(UP/UPS)(通過直腸灌腸給藥)中進行了測試,大多數患者實現了臨床緩解,用於治療潰瘍性結腸炎和克羅恩病的口服布里拉西丁配方的開發取得了進一步的進展。該公司將 UP/UPS 中的 Brilacidin 外包給了 Alfasigma S.p.A. Brilacidin 在中度至重度 COVID-19 住院病例(靜脈注射)的第 2 階段測試中也進行了評估,在患者亞組中觀察到有益的治療效果。生物醫學高級研究與發展局(BARDA)的科學家強調,基於生物標誌物的試驗設計(與特定亞組相關的註冊人數)是提高研究藥物在 COVID-19 和急性肺損傷(ALI)/急性呼吸窘迫綜合徵(ARDS)中實現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.

已向美國專利商標局提交了單獨的專利申請,要求將布里拉西丁用於真菌病。令人鼓舞的 Brilacidin 臨床前結果(體外和體內)已經實現了對抗多種真菌感染,最近發表在一篇文章中 自然通訊,並基於 體外 由獨立研究人員進行的篩選研究。額外 在活體中 計劃在 3Q2023 的功效模型中針對兩種難以治療的真菌病原體進行測試。

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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
Innovation Pharmicals Inc.(IPIX)是一家臨床階段的生物製藥公司,開發一系列創新療法,以滿足包括炎症性疾病、癌症和傳染病在內的多個未滿足的醫療需求。該公司還積極評估其他潛在的投資機會,這些機會可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》的安全港條款發表的前瞻性陳述,包括但不限於有關未來產品開發計劃的聲明,包括有關具體適應症的聲明;關於StingRay系統的治療潛力和能力的聲明;未來的監管發展;以及除歷史事實陳述以外的任何其他陳述。這些陳述涉及風險、不確定性和假設,可能導致實際業績和經驗與這些前瞻性陳述中表達的預期業績和預期存在重大差異。在某些情況下,公司通過使用 “預期”、“相信”、“希望”、“估計”、“外觀”、“期望”、“計劃”、“打算”、“目標”、“潛力”、“可能”、“建議” 等詞語來識別前瞻性陳述。可能導致實際結果與前瞻性陳述中表達的結果存在重大差異的其他因素包括與在美國和其他司法管轄區進行臨床前研究和臨床試驗以及尋求監管和許可批准相關的風險,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,也可能無法獲得監管部門批准在美國或其他地方銷售和銷售;先前的測試結果可能無法在未來的研究中複製試驗;公司未來需要大量資本來爲其運營和研發提供資金,包括根據證券購買協議出售普通股的金額和時間;公司的被許可方可能無法成功完成臨床前或臨床測試,公司也不會獲得里程碑式的付款。公司向美國證券交易委員會提交的文件中包含了對這些和其他風險因素的更完整描述。這些風險、不確定性和假設中有許多超出了公司的控制或預測能力。您不應過分依賴任何前瞻性陳述。前瞻性陳述僅代表公司在發表之日目前獲得的信息,除非適用的法律或法規要求,否則公司沒有義務公開發布對任何此類前瞻性陳述進行的任何修訂的結果,這些修改可能反映本新聞稿發佈之日之後的事件或情況,或者反映意外事件的發生。

INVESTOR AND MEDIA CONTACTS
Innovation Pharmaceuticals Inc.

Leo Ehrlich
info@ipharminc.com

投資者和媒體聯繫人
創新制藥公司
Leo Ehrlich
info@ipharminc.com


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