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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提供有关Brilacidin在炎症性肠病、冠状病毒和真菌疾病中的使用的美国专利申请的最新情况
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."

马萨诸塞州韦克菲尔德,2023年6月21日(GLOBE NEWSWIRE)——通过NewMediaWire——临床阶段的生物制药公司创新制药公司(OTCQB: IPIX)(“公司”)今天宣布,美国专利贸易局(USPTO)于2023年6月6日授予了一项专利,即 “用于预防和/或治疗宿主防御蛋白(HDP)模仿剂胃肠道炎性疾病”,最近还发布了允许申请专利 “用于治疗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.

这些允许的专利分别包括到2036年和2041年对Brilacidin的保护,进一步加强了先前在美国和其他地区授予的Brilacidin知识产权。Brilacidin 是一种模仿宿主防御蛋白的候选药物,具有广谱免疫调节和抗菌特性。

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).

与这些新允许的专利的主张有关,Brilacidin已在溃疡性直肠炎/溃疡性直肠乙状结肠炎(UP/UPS)(通过直肠灌肠给药)中进行了测试,大多数患者实现了临床缓解,用于治疗溃疡性结肠炎和克罗恩病的口服布里拉西丁配方的开发取得了进一步的进展。该公司将 UP/UPS 中的 Brilacidin 外包给了 Alfasigma S.p.A. Brilacidin 在中度至重度 COVID-19 住院病例(静脉注射)的第 2 阶段测试中也进行了评估,在患者亚组中观察到有益的治疗效果。生物医学高级研究与发展局(BARDA)的科学家强调,基于生物标志物的试验设计(与特定亚组相关的注册人数)是提高研究药物在 COVID-19 和急性肺损伤(ALI)/急性呼吸窘迫综合征(ARDS)中实现临床疗效的可能性的关键一步。

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.

已向美国专利商标局提交了单独的专利申请,要求将布里拉西丁用于真菌病。令人鼓舞的 Brilacidin 临床前结果(体外和体内)已经实现了对抗多种真菌感染,最近发表在一篇文章中 自然通讯,并基于 体外 由独立研究人员进行的筛选研究。额外 在活体中 计划在 3Q2023 的功效模型中针对两种难以治疗的真菌病原体进行测试。

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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.

关于创新制药
Innovation Pharmicals Inc.(IPIX)是一家临床阶段的生物制药公司,开发一系列创新疗法,以满足包括炎症性疾病、癌症和传染病在内的多个未满足的医疗需求。该公司还积极评估其他潜在的投资机会,这些机会可以增加价值并使其投资组合多样化。

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.

前瞻性陈述: 本新闻稿包含根据1995年《私人证券诉讼改革法》的安全港条款发表的前瞻性陈述,包括但不限于有关未来产品开发计划的声明,包括有关具体适应症的声明;关于StingRay系统的治疗潜力和能力的声明;未来的监管发展;以及除历史事实陈述以外的任何其他陈述。这些陈述涉及风险、不确定性和假设,可能导致实际业绩和经验与这些前瞻性陈述中表达的预期业绩和预期存在重大差异。在某些情况下,公司通过使用 “预期”、“相信”、“希望”、“估计”、“外观”、“期望”、“计划”、“打算”、“目标”、“潜力”、“可能”、“建议” 等词语来识别前瞻性陈述。可能导致实际结果与前瞻性陈述中表达的结果存在重大差异的其他因素包括与在美国和其他司法管辖区进行临床前研究和临床试验以及寻求监管和许可批准相关的风险,包括但不限于化合物和设备可能无法成功完成临床前或临床测试,也可能无法获得监管部门批准在美国或其他地方销售和销售;先前的测试结果可能无法在未来的研究中复制试验;公司未来需要大量资本来为其运营和研发提供资金,包括根据证券购买协议出售普通股的金额和时间;公司的被许可方可能无法成功完成临床前或临床测试,公司也不会获得里程碑式的付款。公司向美国证券交易委员会提交的文件中包含了对这些和其他风险因素的更完整描述。这些风险、不确定性和假设中有许多超出了公司的控制或预测能力。您不应过分依赖任何前瞻性陈述。前瞻性陈述仅代表公司在发表之日目前获得的信息,除非适用的法律或法规要求,否则公司没有义务公开发布对任何此类前瞻性陈述进行的任何修订的结果,这些修改可能反映本新闻稿发布之日之后的事件或情况,或者反映意外事件的发生。

INVESTOR AND MEDIA CONTACTS
Innovation Pharmaceuticals Inc.

Leo Ehrlich
info@ipharminc.com

投资者和媒体联系人
创新制药公司
Leo Ehrlich
info@ipharminc.com


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