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Citius Pharmaceuticals Announces Closing of $15 Million Registered Direct Offering

Citius Pharmaceuticals Announces Closing of $15 Million Registered Direct Offering

Citius Pharmicals宣佈完成1500萬美元的註冊直接發行
PR Newswire ·  05/01 04:05

CRANFORD, N.J., April 30, 2024 /PRNewswire/ -- Citius Pharmaceuticals Inc. (Nasdaq: CTXR) ("Citius" or the "Company"), a late-stage biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products, today announced that it has closed its previously announced registered direct offering for the purchase of an aggregate of 21,428,574 shares of its common stock and accompanying warrants to purchase up to an aggregate of 21,428,574 shares of its common stock, at a purchase price of $0.70 per share and accompanying warrant. The warrants have an exercise price of $0.75 per share, will be exercisable six months from the date of issuance, and will expire five years from the initial exercise date.

新澤西州克蘭福德,2024年4月30日 /PRNewswire/ — 致力於開發和商業化的後期生物製藥公司Citius Pharmicals Inc.(納斯達克股票代碼:CTXR)(“Citius” 或 “公司”)今天宣佈,已完成先前宣佈的總共21,428,574股股票的註冊直接發行普通股和隨附的認股權證,以每股0.70美元的收購價格購買最多21,428,574股普通股及其附帶的認股權證逮捕令。認股權證的行使價爲每股0.75美元,自發行之日起六個月內可行使,並將自首次行使之日起五年內到期。

H.C. Wainwright & Co. acted 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 were approximately $15 million, before deducting the placement agent fees and other offering expenses payable by the Company. Citius currently intends to use the net proceeds from the offering for general corporate purposes, including pre-clinical and clinical development of our product candidates and working capital and capital expenditures.

在扣除公司應付的配售代理費和其他發行費用之前,公司從本次發行中獲得的總收益約爲1500萬美元。Citius目前打算將本次發行的淨收益用於一般公司用途,包括我們的候選產品的臨床前和臨床開發以及營運資金和資本支出。

The securities described above were offered pursuant to a "shelf" registration statement (File No. 333-277319) filed with the Securities and Exchange Commission ("SEC") on February 23, 2024 and declared effective on March 1, 2024. The offering was made only by means of a prospectus, including a prospectus supplement, forming a part of the effective registration statement. The prospectus supplement and the accompanying prospectus relating to the securities offered was filed with the SEC and is available at the SEC's website at www.sec.gov. Electronic copies of the prospectus supplement and the accompanying prospectus relating to the securities being offered may also be obtained by contacting H.C. Wainwright & Co., LLC at 430 Park Avenue, 3rd Floor, New York, NY 10022, by telephone at (212) 856-5711 or e-mail at [email protected].

上述證券是根據2024年2月23日向美國證券交易委員會(“SEC”)提交的 “貨架” 註冊聲明(文件編號333-277319)發行的,該聲明於2024年3月1日宣佈生效。此次發行僅通過招股說明書(包括招股說明書補充文件)進行,招股說明書是有效註冊聲明的一部分。與所發行證券有關的招股說明書補充文件和隨附的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www.sec.gov上查閱。也可以聯繫位於公園大道 430 號 3 號的 H.C. Wainwright & Co., LLC 獲取招股說明書補充文件和隨附的與所發行證券相關的招股說明書的電子副本第三方 Floor,紐約,紐約 10022,致電 (212) 856-5711 或發送電子郵件至 [email protected]。

This press release shall not constitute an offer to sell or the 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 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 jurisdiction.

本新聞稿不構成出售要約或徵求購買本文所述任何證券的要約,在根據任何此類州或司法管轄區的證券法進行註冊或獲得資格認證之前,在任何州或司法管轄區出售此類證券是非法的,也不得在任何州或司法管轄區出售這些證券。

About Citius Pharmaceuticals, Inc.

關於 Citius 製藥有限公司

Citius is a late-stage biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products. The Company's diversified pipeline includes two late-stage product candidates. The Biologics License Application for LYMPHIR, a novel IL-2R immunotherapy for an initial indication in cutaneous T-cell lymphoma, is currently under review by the FDA with August 13, 2024 assigned as the PDUFA target action date. Citius previously announced plans to form Citius Oncology, a standalone publicly traded company with LYMPHIR as its primary asset. LYMPHIR received orphan drug designation by the FDA for the treatment of CTCL and PTCL. In addition, Citius completed enrollment in its Phase 2b trial of CITI-002 (Halo-Lido), a topical formulation for the relief of hemorrhoids. For more information, please visit .

Citius是一家處於後期階段的生物製藥公司,致力於開發和商業化一流的重症監護產品。該公司的多元化產品線包括兩個處於後期階段的候選產品。LYMPHIR 的生物製劑許可證申請這是一種針對皮膚 T 細胞淋巴瘤初步適應症的新型 IL-2R 免疫療法,目前正在接受美國食品藥品管理局的審查,PDUFA 的目標行動日期定爲 2024 年 8 月 13 日。Citius此前曾宣佈計劃成立Citius Oncology,這是一家以LYMPHIR爲主要資產的獨立上市公司。LYMPHIR被美國食品藥品管理局認定爲用於治療CTCL和PTCL的孤兒藥。此外,Citius完成了其緩解痔瘡的局部配方 CITI-002(Halo-Lido)的2b期試驗的入組。欲了解更多信息,請訪問。

Forward Looking Statements

前瞻性陳述

This press release may contain "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Such statements are made based on our expectations and beliefs concerning future events impacting Citius. You can identify these statements by the fact that they use words such as "will," "anticipate," "estimate," "expect," "plan," "should," and "may" and other words and terms of similar meaning or use of future dates. Forward-looking statements are based on management's current expectations and are subject to risks and uncertainties that could negatively affect our business, operating results, financial condition and stock price, and includes all statements related to the intended use of net proceeds from the offering. Factors that could cause actual results to differ materially from those currently anticipated are: risks relating to the results of research and development activities, including those from existing and new pipeline assets; uncertainties relating to preclinical and clinical testing; the early stage of products under development; our need for substantial additional funds; our ability to commercialize our products if approved by the FDA; our dependence on third-party suppliers; our ability to procure cGMP commercial-scale supply; the estimated markets for our product candidates and the acceptance thereof by any market; the ability of our product candidates to impact the quality of life of our target patient populations; our ability to obtain, perform under and maintain financing and strategic agreements and relationships; market and other conditions; our ability to attract, integrate, and retain key personnel; risks related to our growth strategy; patent and intellectual property matters; our ability to identify, acquire, close and integrate product candidates and companies successfully and on a timely basis; government regulation; competition; as well as other risks described in our SEC filings. These risks have been and may be further impacted by Covid-19 and could be impacted by any future public health risks. Accordingly, these forward-looking statements do not constitute guarantees of future performance, and you are cautioned not to place undue reliance on these forward-looking statements. Risks regarding our business are described in detail in our SEC filings which are available on the SEC's website at www.sec.gov, including in our Annual Report on Form 10-K for the year ended September 30, 2023, filed with the SEC on December 29, 2023, and updated by our subsequent filings with the SEC. These forward-looking statements speak only as of the date hereof, and we expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in our expectations or any changes in events, conditions or circumstances on which any such statement is based, except as required by law.

本新聞稿可能包含1933年《證券法》第27A條和1934年《證券交易法》第21E條所指的 “前瞻性陳述”。此類聲明是基於我們對影響Citius的未來事件的期望和信念做出的。您可以根據這些陳述使用諸如 “將”、“預期”、“估計”、“期望”、“計劃”、“應該” 和 “可能” 等詞語以及其他具有相似含義或使用未來日期的詞彙和術語來識別這些陳述。前瞻性陳述基於管理層當前的預期,受風險和不確定性的影響,這些風險和不確定性可能會對我們的業務、經營業績、財務狀況和股價產生負面影響,幷包括與本次發行淨收益的預期用途有關的所有陳述。可能導致實際結果與目前預期的結果存在重大差異的因素包括:與研發活動結果相關的風險,包括來自現有和新的管道資產的風險;與臨床前和臨床測試相關的不確定性;我們對大量額外資金的需求;如果獲得美國食品藥品管理局批准,我們的產品商業化的能力;我們採購cGMP商業規模供應的能力;我們採購cGMP商業規模供應的能力;估計的市場爲了我們的候選產品及其對任何市場的接受;我們的候選產品影響目標患者群體生活質量的能力;我們獲得、履行和維持融資和戰略協議及關係的能力;市場和其他條件;我們吸引、整合和留住關鍵人員的能力;與增長戰略相關的風險;專利和知識產權事務;我們成功及時識別、收購、關閉和整合候選產品和公司的能力;政府監管;競爭;以及我們在美國證券交易委員會文件中描述的其他風險。這些風險已經並且可能會受到Covid-19的進一步影響,並可能受到未來任何公共衛生風險的影響。因此,這些前瞻性陳述不構成對未來業績的保證,提醒您不要過分依賴這些前瞻性陳述。我們向美國證券交易委員會提交的文件詳細描述了我們的業務風險,這些文件可在美國證券交易委員會網站www.sec.gov上查閱,包括我們在2023年12月29日向美國證券交易委員會提交的截至2023年9月30日止年度的10-K表年度報告,並在隨後向美國證券交易委員會提交的文件中進行了更新。這些前瞻性陳述僅代表截至本文發佈之日,除非法律要求,否則我們明確表示沒有義務或承諾公開發布此處包含的任何前瞻性陳述的任何更新或修訂,以反映我們預期的任何變化或任何此類陳述所依據的事件、條件或情況的任何變化。

Investor Contact:
Ilanit Allen
[email protected]
908-967-6677 x113

投資者聯繫人:
伊拉尼特·艾倫
[電子郵件保護]
908-967-6677 x113

Media Contact:
STiR-communications
Greg Salsburg
[email protected]

媒體聯繫人:
TSI 通信
格雷格·薩爾斯堡
[電子郵件保護]

SOURCE Citius Pharmaceuticals, Inc.

來源 Citius 製藥公司

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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