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GRI Bio Announces Pricing of $4 Million Public Offering

GRI Bio Announces Pricing of $4 Million Public Offering

GRI Bio宣佈定價400萬美元的公開發行。
GRI BIO ·  06/27 12:00

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 the pricing of a public offering of an aggregate of 2,185,793 shares of its common stock (or common stock equivalents in lieu thereof), Series C-1 warrants to purchase up to 2,185,793 shares of common stock and Series C-2 warrants to purchase up to 2,185,793 shares of common stock (all the warrants, collectively, the "Series Warrants"), at a combined public offering price of $1.83 per share (or per common stock equivalent in lieu thereof) and accompanying Series Warrants. The Series Warrants will have an exercise price of $1.83 per share and will be exercisable beginning on the effective date of stockholder approval of the issuance of the shares upon exercise of the Series Warrants. The Series C-1 warrants will expire on the five-year anniversary of the initial exercise date. The Series C-2 warrants will expire on the eighteen month anniversary of the initial exercise date. The closing of the offering is expected to occur on or about June 28, 2024, subject to the satisfaction of customary closing conditions.

加利福尼亞州拉霍亞,2024年6月27日——GRI Bio, Inc.(納斯達克股票代碼:GRI)(“GRI Bio” 或 “公司”)是一家生物技術公司,該公司正在推進用於治療炎症、纖維化和自身免疫性疾病的Natural Killer T(“NKT”)細胞調節劑創新產品線,今天宣佈其普通股(或普通股)的公開發行定價股票等價物代替)、購買最多2,185,793股普通股的C-1系列認股權證和購買最多2,185,793股普通股的C-2系列認股權證(全部認股權證,統稱爲 “系列認股權證”),總公開發行價格爲每股1.83美元(或以每股普通股等價物代替),以及隨附的系列認股權證。系列認股權證的行使價爲每股1.83美元,並將從股東批准行使系列認股權證後發行股票的生效之日起開始行使。C-1系列認股權證將在首次行使之日起五週年之際到期。C-2系列認股權證將在首次行使之日起十八個月週年紀念日到期。此次發行預計將於2024年6月28日左右結束,但須滿足慣例成交條件。

H.C. Wainwright & Co. is acting as the exclusive placement agent for the offering.

H.C. Wainwright & Co. 擔任本次發行的獨家配售代理。

The aggregate gross proceeds to the Company from the offering are expected to be approximately $4 million before deducting the placement agent's fees and other offering expenses payable by the Company. The potential additional gross proceeds to the Company from the Series Warrants, if fully exercised on a cash basis, will be approximately $8 million. No assurance can be given that any of the Series Warrants will be exercised. The Company intends to use the net proceeds from this offering for its product candidate development, working capital and general corporate purposes.

在扣除配售代理費用和公司應付的其他發行費用之前,公司從本次發行中獲得的總收益預計約爲400萬美元。如果以現金爲基礎全部行使,公司可能從該系列認股權證中獲得的額外總收益約爲800萬美元。無法保證任何系列認股權證都會被行使。公司打算將本次發行的淨收益用於其候選產品的開發、營運資金和一般公司用途。

The securities described above are being offered pursuant to a registration statement on Form S-1 (File No. 333-280323), as amended, which was declared effective by the Securities and Exchange Commission (the "SEC") on June 26, 2024. The offering is being made only by means of a prospectus forming part of the effective registration statement relating to the offering. A preliminary prospectus relating to the offering has been filed with the SEC and is available on the SEC's website at http://www.sec.gov and a final prospectus relating to the offering will be filed with the SEC. Electronic copies of the final prospectus, when available, may be obtained on the SEC's website at http://www.sec.gov and may also be obtained, when available, by contacting H.C. Wainwright & Co., LLC at 430 Park Avenue, 3rd Floor, New York, NY 10022, by phone at (212) 856-5711 or e-mail at placements@hcwco.com.

上述證券是根據經修訂的S-1表格(文件編號333-280323)上的註冊聲明發行的,該聲明於2024年6月26日由美國證券交易委員會(“SEC”)宣佈生效。此次發行僅通過招股說明書進行,該招股說明書是與本次發行有關的有效註冊聲明的一部分。與本次發行有關的初步招股說明書已向美國證券交易委員會提交,可在美國證券交易委員會的網站上查閱 http://www.sec.gov 與本次發行有關的最終招股說明書將提交給美國證券交易委員會。最終招股說明書的電子副本(如果有)可在美國證券交易委員會的網站上獲得 http://www.sec.gov 如果有,也可以通過以下方式獲取:聯繫紐約公園大道430號三樓的H.C. Wainwright & Co., LLC,紐約州 10022,電話 (212) 856-5711 或發送電子郵件至 placements@hcwco.com

This press release shall not constitute an offer to sell or a solicitation of an offer to buy any of the securities described herein, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.

本新聞稿不構成出售要約或招攬購買本文所述任何證券的要約,也不得在根據任何此類州或其他司法管轄區的證券法進行註冊或資格認證之前,在任何州或其他司法管轄區出售這些證券是非法的。

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 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是一家臨床階段的生物製藥公司,致力於從根本上改變炎症、纖維化和自身免疫性疾病的治療方式。GRI Bio的療法旨在靶向NKT細胞的活性,NKT細胞是炎症級聯早期的關鍵調節劑,以中斷疾病進展並恢復免疫系統的動態平衡。NKT 細胞是與生俱來的 T 細胞,共有 NK 和 T 細胞的特性,是先天免疫反應和適應性免疫反應之間的功能紐帶。I 型不變 NKT(“inKT”)細胞在傳播炎症和纖維化適應症中觀察到的損傷、炎症反應和纖維化方面起着關鍵作用。GRI Bio的主要項目 GRI-0621 是InKT細胞活性的抑制劑,正在開發爲一種新的口服療法,用於治療特發性肺纖維化,這是一種嚴重的疾病,其需求尚未得到滿足。該公司還在開發用於治療系統性紅斑狼瘡的新型2型NKT激動劑產品線。此外,GRI Bio擁有超過500種專有化合物的庫,有能力爲不斷增長的管道提供燃料。

Forward-Looking Statements

前瞻性陳述

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 completion of the offering; the satisfaction of customary closing conditions related to the offering; the anticipated use of proceeds therefrom; the Company's ability to regain and maintain compliance with Nasdaq's listing requirements; 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, the Company's beliefs and expectations regarding potential stakeholder value and future financial performance 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 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1995年《私人證券訴訟改革法》中 “安全港” 條款所指的 “前瞻性陳述”。前瞻性陳述可以通過使用 “預測”、“相信”、“考慮”、“可以”、“估計”、“期望”、“打算”、“尋求”、“可能”、“可能”、“計劃”、“潛在”、“預測”、“項目”、“目標”、“應該”、“將”、“將” 等詞語或這些詞語的否定詞來識別或其他類似的表達方式。這些前瞻性陳述基於公司當前的信念和預期。前瞻性陳述包括但不限於以下方面的陳述:本次發行的完成;與發行相關的慣例成交條件的滿足;所得收益的預期用途;公司恢復和維持遵守納斯達克上市要求的能力;公司對公司候選產品的開發和商業化的預期、臨床試驗啓動或完成的時機以及所得數據的可用性、潛在的收益和影響公司的臨床試驗和候選產品,以及任何暗示在臨床前試驗或早期研究或試驗中觀察到的數據或結果將表明後來的研究或臨床試驗結果、公司對潛在利益相關者價值和未來財務業績的信念和期望,以及公司對監管批准的時間和結果以及潛在的監管批准途徑的看法。實際業績可能與公司在本新聞稿中表達的前瞻性陳述有所不同,因此,您不應依賴這些前瞻性陳述作爲對未來事件的預測。這些前瞻性陳述受難以預測的固有不確定性、風險和假設的影響,包括但不限於:(1)無法維持公司普通股在納斯達克的上市和遵守適用的上市要求;(2)適用法律或法規的變化;(3)公司未來無法籌集資金;(4)公司產品開發活動的成功、成本和時機;(5)無法爲了獲得和維持監管許可,或者其各自產品的批准,以及對任何已批准或批准的產品的任何相關限制和限制;(6) 公司無法識別、許可或獲取其他技術;(7) 公司無法與目前正在銷售或參與開發公司目前正在開發的產品和服務的其他公司競爭;(8) 公司產品和服務市場的規模和增長潛力,以及它們各自爲這些市場服務的能力,單獨或與他人合作其他;(9)未能實現任何里程碑或根據任何協議獲得任何里程碑付款;(10)公司對支出、未來收入、資本要求和額外融資需求和獲得額外融資能力的估計不準確;(11)公司保護和執行其知識產權組合,包括任何新發行的專利的能力;以及(12)公司向美國證券交易委員會提交的文件中不時顯示的其他風險和不確定性,包括 “風險因素” 中描述的風險和不確定性公司於2024年3月28日向美國證券交易委員會提交的最新10-K表年度報告的一部分,隨後提交了報告。本公告中包含的前瞻性陳述自該日起作出,除非適用法律要求,否則公司沒有義務更新此類信息。

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

投資者聯繫人:
JTC Team, LLC
珍妮·托馬斯
(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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