Citius Pharmaceuticals Announces $3 Million Registered Direct Offering
Citius Pharmaceuticals Announces $3 Million Registered Direct Offering
CRANFORD, N.J., Nov. 15, 2024 /PRNewswire/ -- Citius Pharmaceuticals Inc. (Nasdaq: CTXR) ("Citius Pharma" or the "Company"), a biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products, today announced that it has entered into definitive agreements for the purchase of an aggregate of 12,000,000 shares of its common stock and accompanying warrants to purchase up to an aggregate of 12,000,000 shares of its common stock, at a purchase price of $0.25 per share and accompanying warrant in a registered direct offering. The warrants will have an exercise price of $0.25 per share, will be exercisable immediately upon issuance, and will expire five years from the initial exercise date. The closing of the offering is expected to occur on or about November 18, 2024, subject to the satisfaction of customary closing conditions.
CRANFORD,新泽西州,2024年11月15日 / PRNewswire / - Citius Pharmaceuticals Inc.(纳斯达克:CTXR)("Citius Pharma"或"公司"),一家致力于开发和商业化一流急救产品的生物制药公司,今天宣布已签署明确协议,购买总计12,000,000股普通股及关联权证,该关联权证可购买总计12,000,000股普通股,购买价为每股$0.25及附赠权证,在注册直接发行中。权证行使价为每股$0.25,发行后即可行使,并将于首次行使日期起计有效五年。该发行预计将于2024年11月18日前后完成,具体时间取决于完成通常的交割条件。
H.C. Wainwright & Co. is acting as the exclusive placement agent for the offering.
H.C.Wainwright & Co.将担任本次定向增发的独家配售代理。
The aggregate gross proceeds to the Company from the offering are expected to be $3 million, before deducting the placement agent fees and other offering expenses payable by the Company. The Company 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.
本次发行预期将为公司带来总计$3,000,000的募集净收入,扣除由公司支付的征位代理费和其他发行费用。公司目前打算利用本次发行的净收益用于一般公司用途,包括产品候选物的临床前和临床开发以及运营资金和资本支出。
The securities described above are being 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 is being 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 being offered will be filed with the SEC and be 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, when available, 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].
上述证券是根据已于2024年2月23日提交的"货架"注册声明(文件号333-277319)进行发行的,并于2024年3月1日宣告生效。本次发行仅通过一份招股说明书进行,包括构成有效注册声明一部分的招股说明书补充说明书。将与本次发行的证券相关的招股说明书补充说明书和附属招股说明书将提交给SEC,并可在SEC的网站www.sec.gov上获得。本次发行的招股说明书补充说明书和附属招股说明书的电子副本也可通过联系H.C. Wainwright & Co., LLC获取,地址为New York, NY 10022,Park Avenue 430号3楼,电话:(212)856-5711或电子邮件:[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.
本新闻稿不构成出售或购买本处所述任何证券的要约,也不得在此类要约、招揽或出售被认为是违法的州或司法管辖区内,在该州或司法管辖区注册或符合证券法规定之前出售这些证券。
About Citius Pharmaceuticals, Inc.
关于Citius Pharmaceuticals,Inc。
Citius Pharma is a biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products. In August 2024, the FDA approved LYMPHIR, a targeted immunotherapy for an initial indication in the treatment of cutaneous T-cell lymphoma. Citius Pharma's late-stage pipeline also includes Mino-Lok, an antibiotic lock solution to salvage catheters in patients with catheter-related bloodstream infections, and CITI-002 (Halo-Lido), a topical formulation for the relief of hemorrhoids. A Pivotal Phase 3 Trial for Mino-Lok and a Phase 2b trial for Halo-Lido were completed in 2023. Mino-Lok met primary and secondary endpoints of its Phase 3 Trial. Citius Pharma is actively engaged with the FDA to outline next steps for both programs. Citius Pharma owns 92% of Citius Oncology, Inc. ("Citius Oncology"). For more information, please visit .
Citius Pharma是一家生物制药公司,致力于开发和商业化首个类关键护理产品。2024年8月,FDA批准了LYMPHIR,这是一种针对治疗皮肤T细胞淋巴瘤初始适应症的靶向免疫疗法。Citius Pharma的晚期产品线还包括Mino-Lok,一种抗生素锁定溶液,可用于拯救患有导管相关血流感染的患者的导管,以及CITI-002(Halo-Lido),一种用于缓解痔疮症状的局部制剂。2023年,Mino-Lok的关键3期试验和Halo-Lido的第20亿期试验已经完成。Mino-Lok满足了其关键3期试验的首要和次要终点。Citius Pharma正在与FDA积极合作,制定这两个项目的下一步计划。Citius Pharma拥有Citius Oncology,Inc.(“Citius Oncology”)92%的股份。欲了解更多信息,请访问。
Forward Looking Statements
前瞻性声明
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 Pharma. 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 completion of the offering, the satisfaction of customary closing conditions related to the offering and the intended use of net proceeds from the offering. Factors that could cause actual results to differ materially from those currently anticipated, and, unless noted otherwise, that apply to Citius Pharma and Citius Oncology, are: related to the closing of the offering; our ability to raise additional money to fund our operations for at least the next 12 months as a going concern; Citius Pharma's ability to regain compliance with and continue to meet Nasdaq's continued listing standards; our ability to commercialize LYMPHIR and any of our other product candidates that may be approved by the FDA; risks relating to the results of research and development activities, including those from our existing and any new pipeline assets; risks related to research using our assets but conducted by third parties; our need for substantial additional funds; 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 dependence on third-party suppliers; our ability to procure cGMP commercial-scale supply; our ability to obtain, perform under and maintain financing and strategic agreements and relationships; uncertainties relating to preclinical and clinical testing; the early stage of products under development; market and other conditions; 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 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 Citius Pharma's Annual Report on Form 10-K for the year ended September 30, 2023, filed with the SEC on December 29, 2023, as 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.
本新闻稿可能包含符合1933年证券法第27A条和1934年证券交易法第21E条的“前瞻性声明”。此类声明根据我们对影响Citius Pharma的未来事件的预期和信念进行。您可以通过这些声明来识别它们使用“将”,“预期”,“估计”,“期望”,“计划”,“应该”和“可能”等词汇以及其他具有类似含义或使用未来日期的词语。前瞻性声明基于管理层目前的期望,并且受到可能对我们业务,运营结果,财务状况和股价产生负面影响的风险和不确定性的影响,其中包括与完成发行有关的一切声明,与发行相关的惯例终结条件的满足以及发行的净收益的预期用途。可能导致实际结果与当前预期有实质差异的因素,除非另有说明,这些因素适用于Citius Pharma和Citius Oncology:与发行闭环有关的风险;我们能够筹集足够资金以维持至少未来12个月的运营作为持续经营的能力;Citius Pharma能够恢复并继续符合纳斯达克的继续上市标准;我们能够推广LYMPHIR以及FDA可能批准的我们其他任何产品候选药物的能力;与研究开发活动的结果相关的风险,包括我们现有和任何新的管道资产;由第三方进行研究使用我们资产而进行的研究相关风险;我们需要大量额外资金;我们的产品候选药物的预估市场及其及其接受程度;我们的产品候选药物对我们目标患者人群生活质量的影响能力;我们依赖于第三方供应商;我们能够获得cGMP商业规模供应;我们能够获得,执行和维持融资和战略协议和关系的能力;与临床和临床试验有关的不确定性;产品开发早期阶段;市场和其他状况;与增长战略相关的风险;专利和知识产权事项;我们成功识别,收购,关闭和整合产品候选和公司的能力以及及时的基础;政府管理;竞争;以及其他在我们的SEC备案中描述的风险。这些风险一直可以并且或许会受到未来公共卫生风险的进一步影响。因此,这些前瞻性声明并不能构成未来表现的保证,并且我们警告您不要过分依赖这些前瞻性声明。有关我们业务的风险在我们的SEC备案中有详细描述,这些备案可以在SEC网站www.sec.gov上获得,包括Citius Pharma于2023年12月29日向SEC提交的截至2023年9月30日年度报告表格10-k,以及我们随后向SEC提交的备案文件。这些前瞻性声明仅在此日期发表,我们明确放弃对这些在此包含的前瞻性声明发布公开更新或修订的任何义务或承诺,以反映任何现有我们的期望或所依赖的事件,状况或环境的任何变化, 除非法律要求。
Investor Contact:
Ilanit Allen
[email protected]
908-967-6677 x113
投资者联系人:
Ilanit Allen
[email protected]
908-967-6677 x113
Media Contact:
STiR-communications
Greg Salsburg
[email protected]
媒体联系:
STiR-communications
Greg Salsburg
[email protected]
SOURCE Citius Pharmaceuticals, Inc.
来源:Citius Pharmaceuticals, Inc.