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Tonix Pharmaceuticals Announces Closing of $4.0 Million Public Offering

Tonix Pharmaceuticals Announces Closing of $4.0 Million Public Offering

tonix pharmaceuticals宣佈完成400萬美元公開發行。
Tonix Pharmaceuticals ·  07/10 00:00

Tonix Pharmaceuticals Announces Closing of $4.0 Million Public Offering

tonix pharmaceuticals宣佈完成400萬美元公開發行。

July 10, 2024 4:30pm EDT Download as PDF
2024年7月10日下午4:30 EDt 保存爲PDF

CHATHAM, N.J., July 10, 2024 (GLOBE NEWSWIRE) -- Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) ("Tonix" or the "Company"), a fully-integrated biopharmaceutical company, today announced the closing of its public offering of 3,393,600 shares of its common stock and pre-funded warrants to purchase up to 3,703,140 shares of common stock in a public offering at an offering price of $0.57 per share of common stock and $0.569 per pre-funded warrant. The warrants have an exercise price of $0.001 per share and became exercisable upon issuance.

新澤西州查塔姆,2024年7月10日(環球新聞通訊社)——安泰醫藥控股公司(納斯達克:TNXP)("安泰"或"公司")是一家全面集成的生物製藥公司,今天宣佈,公司以每股0.57美元的發行價,公開發行339.36萬股普通股和可提前行使購買最多370.314萬股普通股的預先擔保認購權。認購權的行使價格爲每股0.001美元,自發行日起行使。

The gross proceeds of the offering are $4.0 million before deducting placement agent fees and other estimated offering expenses payable by the Company. The Company intends to use the net proceeds from the offering for working capital and general corporate purposes, including the preparation of the new drug application relating to its Tonmya product candidate in patients with fibromyalgia, and the satisfaction of any portion of its existing indebtedness.

發行市值爲4,000,000美元,扣除放置代理費用和其他估計的發行費用,由公司支付。公司打算將發行所得用於營運資金和一般公司目的,包括準備與其用於治療纖維肌痛患者的Tonmya候選藥品相關的新藥申請,以及償還任何部分現有債務。

Dawson James Securities, Inc. acted as the sole placement agent for the offering.

Dawson James Securities, Inc.擔任本次發行的唯一放置代理。

Lowenstein Sandler, New York, NY, represented the Company in connection with the offering, and ArentFox Schiff LLP, Washington, DC, represented the placement agent.

紐約市洛因斯坦薩德勒律師事務所代表公司參與發行,而ArentFox Schiff律師事務所(華盛頓特區)則代表放置代理。

This offering was made pursuant to an effective shelf registration statement on Form S-3 (File No. 333-266982) previously filed with the U.S. Securities and Exchange Commission (the "SEC"). The offering was made only by means of a prospectus supplement and accompanying prospectus. A final prospectus supplement and accompanying prospectus describing the terms of the proposed offering were filed with the SEC and are available on the SEC's website located at Electronic copies of the preliminary prospectus supplement may be obtained from Dawson James Securities, Inc., 101 North Federal Highway, Suite 600, Boca Raton, FL 33432 or by telephone at (561) 391-5555, or by email at investmentbanking@dawsonjames.com.

本次發行是依據先前向美國證券交易委員會("SEC")提交的S-3表格(文件編號333-266982)有效的架構註冊聲明執行的。該發行僅通過招股書補充和附帶的招股說明書進行。最終招股書補充和附帶的招股說明書描述了擬議發行的條款,並已提交給SEC並可在位於SEC網站上獲取的。初步招股說明書的電子副本可從Dawson James Securities,Inc.,101 North Federal Highway,Suite 600,Boca Raton,FL 33432獲得,或通過電話(561)391-5555或電子郵件investmentbanking@dawsonjames.com獲得。

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

Tonix Pharmaceuticals Holding Corp.*,是一家完全整合的生物製藥公司,致力於發展富有創新性的治療和預防潛在疾病的製劑。公司正在研發針對纖維肌痛患者的產品TNX-102 SL,已經完成了兩項具有統計學意義的3期研究。TNX-102 SL也正在被開發用於治療急性壓力反應以及類纖維肌痛的長期COVID。Tonix的神經系統藥物組合包括TNX-1300(可卡因酯酶),這是一種用於治療可卡因中毒、被授予“突破性療法”稱號的生物製品。Tonix的免疫學研發組合包括生物製品,用於治療器官移植排斥、自身免疫和癌症,包括TNX-1500,這是一種人源單克隆抗體,靶向CD40L(CD40L或CD154)用於預防異體移植器官排斥並用於治療自身免疫性疾病。Tonix在罕見疾病和傳染病領域的正在研發中的產品。商業子公司Tonix Medicines市場上銷售Zembrace SymTouch(舒馬曲坦注射液)3毫克和Tosymra(舒馬曲坦鼻噴劑)10毫克,用於成年急性偏頭疼的治療。

Tonix Pharmaceuticals Holding Corp.*

Tonix Pharmaceuticals Holding Corp.*

Tonix is a fully-integrated biopharmaceutical company focused on developing, licensing and commercializing therapeutics to treat and prevent human disease and alleviate suffering. Tonix's development portfolio is focused on central nervous system (CNS) disorders. Tonix's priority is to submit a New Drug Application (NDA) to the FDA in the second half of 2024 for Tonmya1, a product candidate for which two statistically significant Phase 3 studies have been completed for the management of fibromyalgia. TNX-102 SL is also being developed to treat acute stress reaction as well as fibromyalgia-type Long COVID. Tonix's CNS portfolio includes TNX-1300 (cocaine esterase), a biologic designed to treat cocaine intoxication that has Breakthrough Therapy designation. Tonix's immunology development portfolio consists of biologics to address organ transplant rejection, autoimmunity and cancer, including TNX-1500, which is a humanized monoclonal antibody targeting CD40-ligand (CD40L or CD154) being developed for the prevention of allograft rejection and for the treatment of autoimmune diseases. Tonix also has product candidates in development in the areas of rare disease and infectious disease. Tonix Medicines, our commercial subsidiary, markets Zembrace SymTouch (sumatriptan injection) 3 mg and Tosymra (sumatriptan nasal spray) 10 mg for the treatment of acute migraine with or without aura in adults.

Tonix是一家全面集成的生物製品公司,專注於開發、許可和銷售用於治療和預防人類疾病和減輕痛苦的治療劑。Tonix的發展合作伙伴的組合主要集中在中樞神經系統(CNS)疾病。Tonix的重點是在2024年下半年向美國FDA遞交Tonmya1的新藥申請(NDA),Tonmya1是一種用於治療纖維肌痛的產品,已完成兩項有統計學意義的III期研究。TNX-102 SL也正在開發,用於治療急性壓力反應以及纖維肌痛型長週期感染。Tonix的CNS產品組合包括TNX-1300(可卡因酯酶),一種用於治療可卡因中毒的生物製品,已獲得突破性療法認定。 Tonix的免疫學開發組合包括用於肝臟移植排斥反應、自身免疫病和癌症的生物製品,包括TNX-1500,該生物製品是一種人源化單克隆抗體靶向CD40-Ligand (CD40L或CD154),正在開發用於預防異種移植排斥及治療自身免疫性疾病。Tonix在罕見疾病和感染性疾病領域的藥品候選品也正在研發。Tonix Medicines是Tonix的商業子公司,主要市場營銷的藥品是治療成人急性偏頭痛和無偏頭痛的口服舒米特蘭注射液Zembrace SymTouch(蘇米替丹注射液)3毫克和鼻腔噴霧劑Tosymra(蘇米替丹鼻腔噴霧劑)10毫克。

*Tonix's product development candidates are investigational new drugs or biologics and have not been approved for any indication.

Tonix的產品研發候選品是新藥或生物製品,尚未獲得任何適應症批准。

1Tonmya is conditionally accepted by the U.S. Food and Drug Administration (FDA) as the tradename for TNX-102 SL for the management of fibromyalgia. Tonmya has not been approved for any indication.

1Tonmya被美國食品藥品監督管理局(FDA)有條件地接受爲TNX-102 SL治療纖維肌痛的商品名稱。Tonmya尚未獲得任何適應症的批准。

Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. All other marks are property of their respective owners.

Zembrace SymTouch和Tosymra是Tonix Medicines的註冊商標,其他所有商標均爲其各自所有者的財產。

This press release and further information about Tonix can be found at .

有關Tonix的此新聞稿和更多信息,請訪問。

Forward Looking Statements

前瞻性聲明

Certain statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995 including those relating to the intended use of proceeds from the public offering and other statements that are predictive in nature. These statements may be identified by the use of forward-looking words such as "anticipate," "believe," "forecast," "estimate," "expect," and "intend," among others. These forward-looking statements are based on Tonix's current expectations and actual results could differ materially. There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements. These factors include, but are not limited to, risks related to the failure to obtain FDA clearances or approvals and noncompliance with FDA regulations; risks related to the failure to successfully market any of our products; risks related to the timing and progress of clinical development of our product candidates; our need for additional financing; uncertainties of patent protection and litigation; uncertainties of government or third party payor reimbursement; limited research and development efforts and dependence upon third parties; and substantial competition. As with any pharmaceutical under development, there are significant risks in the development, regulatory approval and commercialization of new products. Tonix does not undertake an obligation to update or revise any forward-looking statement. Investors should read the risk factors set forth in the Annual Report on Form 10-K for the year ended December 31, 2023, as filed with the Securities and Exchange Commission (the "SEC") on April 1, 2024, and periodic reports filed with the SEC on or after the date thereof. All of Tonix's forward-looking statements are expressly qualified by all such risk factors and other cautionary statements. The information set forth herein speaks only as of the date thereof.

本新聞稿中的某些陳述屬於《1995年私人證券訴訟改革法案》中的前瞻性陳述,包括關於公開發行所得使用目的的陳述和其他具有預測性質的陳述。這些陳述可通過使用前瞻性詞語,例如“預期”,“相信”,“預測”,“估計”,“期望”和“打算”等來區分。這些前瞻性陳述基於Tonix目前的預期,實際結果可能有所不同。有許多因素可能導致實際情況與此類前瞻性陳述所示情況不符。這些因素包括但不限於,與FDA清關或批准相關的風險以及與FDA法規不符的風險;營銷任何產品的失敗風險;產品候選物的臨床開發進展和時間風險;我們需要增加資金;專利保護和訴訟的不確定性;政府或第三方支付者退款的不確定性;有限的研究和開發工作以及對第三方的依賴以及激烈的競爭。與正在開發的任何製藥品一樣,新產品的開發、法規批准和商業化都存在重大風險。Tonix不承擔更新或修訂任何前瞻性聲明的義務。投資者應閱讀年度報告,該報告已於2024年4月1日提交給證券交易委員會(SEC),並閱讀此後提交給SEC的定期報告,以獲取有關此類風險的因素。所有Tonix的前瞻性陳述都經過此類風險因素和其他謹慎性聲明的明確限定。此處的信息僅截止當日。

Investor Contact

投資者聯繫方式

Jessica Morris
Tonix Pharmaceuticals
investor.relations@tonixpharma.com
(862) 904-8182

Jessica Morris
tonix pharmaceuticals
investor.relations@tonixpharma.com
(862) 904-8182

Peter Vozzo
ICR Westwicke
peter.vozzo@westwicke.com
(443) 213-0505

Peter Vozzo
ICR Westwicke
peter.vozzo@westwicke.com
(443) 213-0505

Media Contact

媒體聯繫人

Katie Dodge
LaVoieHealthScience
kdodge@lavoiehealthscience.com
(978) 360-3151

Katie Dodge
LaVoieHealthScience
kdodge@lavoiehealthscience.com
(978) 360-3151


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Source: Tonix Pharmaceuticals Holding Corp.
來源:Tonix製藥公司

Released July 10, 2024

發佈於2024年7月10日

声明:本內容僅用作提供資訊及教育之目的,不構成對任何特定投資或投資策略的推薦或認可。 更多信息
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