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GRI Bio Announces Korea Patent Granted for Proprietary Natural Killer T (NKT) Cell Modulators

GRI Bio Announces Korea Patent Granted for Proprietary Natural Killer T (NKT) Cell Modulators

GRI Bio宣佈獲得韓國專利,專利涉及其自有的自然殺傷T細胞(NKT細胞)調節劑。
GRI BIO ·  06/27 12:00

Company is strategically building a global patent estate in key territories for a growing pipeline targeting potentially high-value indications in need of innovation

公司正在爲不斷增長的種植物管道在關鍵領域戰略性地建立全球專利組合,以針對潛在的需要創新高價值指示的目標。

LA JOLLA, CA, June 27, 2024 — GRI Bio, Inc. (NASDAQ: GRI) ("GRI Bio" or the "Company"), a biotechnology company advancing an innovative pipeline of Natural Killer T (NKT) cell modulators for the treatment of inflammatory, fibrotic and autoimmune diseases, today announced that the Korean Intellectual Property Office (KIPO) has granted Patent No. 10-2665487 titled, "Prevention and Treatment of Inflammatory Conditions."

2024年6月27日,位於卡拉霍,加利福尼亞州的GRI Bio公司(NASDAQ: GRI) (以下簡稱"GRI Bio"或"公司"),一家生物技術公司正在推進一種創新的天然殺傷T細胞調節劑管道,用於治療炎症、纖維化和自身免疫性疾病,今天宣佈,韓國知識產權局(KIPO)已授予專利編號10-2665487,標題爲"授予專利涵蓋了調節型2和/或型1不變量NKT(iNKT)細胞以預防和治療炎症性疾病的組合物和方法,更具體地說,該專利涵蓋了通過將抑制iNKT細胞的RAR激動劑給予受試者來預防和治療炎症、纖維化和自身免疫性疾病的組合物和方法。."

The granted patent covers claims including compositions and methods for modulating type 2 and/or type 1 invariant NKT (iNKT) cells in the prevention and treatment of inflammatory conditions. More specifically, the patent covers the prevention and treatment of inflammatory, fibrotic and autoimmune conditions through the administration of a Retinoic Acid Receptor (RAR) agonist that inhibits iNKT cells in a subject.

缺乏創新的炎症性、纖維化和自身免疫性疾病的預防和治療,是一項重大的未遂任務。該授予的專利可以爲人們提供一種新的和有效的方法,即通過抑制iNKT細胞的活性,利用RAR激動劑阻止一些被認爲是過度引發這些疾病的免疫細胞的活性。

"We wholeheartedly believe in our highly differentiated approach to the prevention and treatment of inflammatory, fibrotic and autoimmune diseases. We are pleased to now have this Korea patent granted and added to our intellectual property portfolio covering our innovative pipeline of NKT cell modulators. Our primary focus is on advancing our clinical development programs and look forward to announcing interim data from our lead program GRI-0621 for our Phase 2a biomarker study in the third quarter of this year," Marc Hertz, PhD, Chief Executive Officer of GRI Bio.

“我們全心全意地相信我們對預防和治療炎症、纖維化和自身免疫性疾病的高度差異化方法。我們很高興現在已經被授權這項韓國專利,並將其添加到我們的知識產權組合中,涵蓋我們的創新NKT細胞調節劑管道。我們的主要重點是推進我們的臨床開發計劃,期待今年第三季度在我們領先的GRI-0621的第2期生物標誌物研究中宣佈中期數據,”GRI Bio首席執行官Marc Hertz博士表示。

GRI Bio is currently advancing its lead program GRI-0621, a small molecule RAR-βɣ dual agonist candidate that inhibits the activity of human iNKT cells, in a Phase 2a, randomized, double-blind, multi-center, placebo-controlled, parallel-design, 2-arm study for the treatment of Idiopathic Pulmonary Fibrosis (IPF). IPF is a rare chronic progressive pulmonary disease with abnormal scarring of the lung blocking the movement of oxygen into the bloodstream. Topline results from this study are expected in the fourth quarter of 2024.

GRI Bio正在推進其領先的項目GRI-0621,這是一種小分子RAR-βɣ雙激動劑候選藥物,可抑制人iNKT細胞的活性,用於治療特發性肺纖維化(IPF)的第2A期,隨機、雙盲、多中心、安慰劑對照、平行設計、2臂研究。IPF是一種罕見的慢性進行性肺部疾病,長期的肺部瘢痕會阻礙氧氣進入血液中。該研究的初步結果預計將於2024年第四季度公佈。

For more information about the Company's innovative pipeline of NKT cell regulators for the treatment of inflammatory, fibrotic and autoimmune diseases, visit gribio.com.

了解更多有關公司針對炎症、纖維化和自身免疫性疾病的創新NKT細胞調節器管道的信息,請訪問gribio.com.

About GRI Bio, Inc.

關於GRI Bio, Inc.

GRI Bio is a clinical-stage biopharmaceutical company focused on fundamentally changing the way inflammatory, fibrotic and autoimmune diseases are treated. GRI Bio's therapies are designed to target the activity of Natural Killer T ("NKT") cells, which are key regulators earlier in the inflammatory cascade, to interrupt disease progression and restore the immune system to homeostasis. NKT cells are innate-like T cells that share properties of both NK and T cells and are a functional link between the innate and adaptive immune responses. Type I invariant NKT ("iNKT") cells play a critical role in propagating the injury, inflammatory response, and fibrosis observed in inflammatory and fibrotic indications. GRI Bio's lead program, GRI-0621, is an inhibitor of iNKT cell activity and is being developed as a novel oral therapeutic for the treatment of idiopathic pulmonary fibrosis, a serious disease with significant unmet need. The Company is also developing a pipeline of novel type 2 NKT agonists for the treatment of systemic lupus erythematosus. Additionally, with a library of over 500 proprietary compounds, GRI Bio has the ability to fuel a growing pipeline.

GRI Bio是一家專注於根本性改變炎症、纖維化和自身免疫性疾病治療方式的臨床階段生物製藥公司。GRI Bio的產品旨在針對自然殺傷T(“NKT”)細胞的活性,這些細胞是炎症級聯早期的關鍵調節因子,以打斷疾病進展和恢復免疫系統的穩態。NKT細胞是具有NK和T細胞性質的先天樣T細胞,是先天和適應性免疫反應之間的功能性鏈接。I型不變NKT(“iNKT”)細胞在炎症和纖維化症狀中發揮關鍵作用。 GRI Bio的主導項目GRI-0621是iNKT細胞活性抑制劑,正在開發作爲治療特發性肺纖維化的新型口服藥物,這是一種有重大未滿足需求的嚴重疾病。該公司還正在開發一系列新型2型NKT激動劑,用於治療系統性紅斑狼瘡。此外,GRI Bio擁有超過500種專有化合物的庫,可爲其不斷壯大的管道提供動力。

Forward-Looking Statements

前瞻性聲明

This press release contains "forward-looking statements" within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by the use of words such as "anticipate," "believe," "contemplate," "could," "estimate," "expect," "intend," "seek," "may," "might," "plan," "potential," "predict," "project," "target," "aim," "should," "will," "would," or the negative of these words or other similar expressions. These forward-looking statements are based on the Company's current beliefs and expectations. Forward-looking statements include, but are not limited to, statements regarding: the Company's expectations with respect to development and commercialization of the Company's product candidates, the timing of initiation or completion of clinical trials and availability of resulting data, the potential benefits and impact of the Company's clinical trials and product candidates and any implication that the data or results observed in preclinical trials or earlier studies or trials will be indicative of results of later studies or clinical trials and the Company's beliefs about the timing and outcome of regulatory approvals and potential regulatory approval pathways. Actual results may differ from the forward-looking statements expressed by the Company in this press release and consequently, you should not rely on these forward-looking statements as predictions of future events. These forward-looking statements are subject to inherent uncertainties, risks and assumptions that are difficult to predict, including, without limitation: (1) the inability to maintain the listing of the Company's common stock on Nasdaq and to comply with applicable listing requirements; (2) changes in applicable laws or regulations; (3) the inability of the Company to raise financing in the future; (4) the success, cost and timing of the Company's product development activities; (5) the inability of the Company to obtain and maintain regulatory clearance or approval for its respective products, and any related restrictions and limitations of any cleared or approved product; (6) the inability of the Company to identify, in-license or acquire additional technology; (7) the inability of the Company to compete with other companies currently marketing or engaged in the development of products and services that the Company is currently developing; (8) the size and growth potential of the markets for the Company's products and services, and their respective ability to serve those markets, either alone or in partnership with others; (9) the failure to achieve any milestones or receive any milestone payments under any agreements; (10) inaccuracy in the Company's estimates regarding expenses, future revenue, capital requirements and needs for and the ability to obtain additional financing; (11) the Company's ability to protect and enforce its intellectual property portfolio, including any newly issued patents; and (12) other risks and uncertainties indicated from time to time in the Company's filings with the U.S. Securities and Exchange Commission (the "SEC"), including the risks and uncertainties described in the "Risk Factors" section of the Company's most recent Annual Report on Form 10-K filed with the SEC on March 28, 2024 and subsequently filed reports. Forward-looking statements contained in this announcement are made as of this date, and the Company undertakes no duty to update such information except as required under applicable law.

本新聞稿包含“前瞻性聲明”,根據1995年《私人證券訴訟改革法》的“安全港”條款,該條款規定可通過使用諸如“預計”、“相信”、“思考”、“可能”、“估計”、“期望”、“打算”、“尋求”、“可能”、“計劃”、“潛在”、“預測”、“項目”、“目標”、“瞄準”、“應該”、“將”、“願意”或其他類似表達方式的用詞來識別前瞻性聲明。這些前瞻性聲明基於本公司目前的信念和期望。前瞻性聲明包括但不限於:關於公司產品候選品的開發和商業化的期望,臨床試驗的啓動或完成時間以及得出的數據的可用性,公司臨床試驗和產品候選品的潛在益處和影響以及任何意味着臨床試驗或前期試驗或研究中觀察到的數據或結果將預示後期試驗或臨床試驗結果的聲明,以及公司對監管批准的時機和結果以及潛在的監管批准途徑的信念。本新聞稿中的前瞻性聲明基於本公司目前的信念和期望。本新聞稿中的前瞻性聲明取決於內在的不確定性、風險和假設,這些不確定性、風險和假設很難預測,包括但不限於:(1)無法保持公司普通股在NASDAQ的上市,並遵守適用的上市要求;(2)適用法律或法規的變化;(3)公司將來無法籌集資金;(4)公司產品開發活動的成功、成本和時間;(5)公司無法爲其各自的產品獲得和維持法規審批或批准,以及任何獲得批准的產品的相關限制和限制;(6)公司無法識別、許可或收購其他技術;(7)公司無法與目前市場營銷或從事與公司目前開發產品和服務相同的產品和服務的其他公司競爭;(8)公司的產品和服務市場的大小和增長潛力,以及其各自能否獨自或與其他公司合作爲這些市場提供服務;(9)未能在任何協議下達到任何里程碑或獲得任何里程碑付款;(10)對於支出、未來收入、資本需求和需要和能否獲得額外融資的估計不準確;(11)公司保護和執行其知識產權組合,包括任何新頒發的專利的能力;以及(12)其他風險和不確定因素,時不時地註明在公司向美國證券交易委員會(SEC)提交的文件中,包括在2024年3月28日提交的公司最新一份年度報告(Form 10-K)的“風險因素”部分以及隨後提交的報告中所描述的風險和不確定因素。本公告中的前瞻性聲明截至此日期,公司無義務更新此類信息,除非根據適用法律要求。

Investor Contact:
JTC Team, LLC
Jenene Thomas
(833) 475-8247
GRI@jtcir.com

投資者聯繫人:
JTC團隊有限責任公司
Jenene Thomas
(833) 475-8247
GRI@jtcir.com

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譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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