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Aridis Pharmaceuticals Announces $2 Million Offering

Aridis Pharmaceuticals Announces $2 Million Offering

阿瑞迪斯制药宣布发行200万美元
GlobeNewswire ·  2023/08/02 08:17

Los Gatos, Calif., Aug.  02, 2023  (GLOBE NEWSWIRE) -- Aridis Pharmaceuticals, Inc. (OTC: ARDS), a biopharmaceutical company focused on the discovery and development of novel anti-infective therapies for treating life-threatening infections, today announced the pricing of an offering of 10,000,000 shares of the Company's common stock (or pre-funded warrants in lieu thereof) and accompanying warrants to purchase up to 10,000,000 shares of common stock at a combined offering price of $0.20 per share of common stock (or pre-funded warrant) and accompanying warrant. Each warrant will have an exercise price per share of $0.20, will be exercisable immediately and will terminate on the five year anniversary of the date of issuance. The closing of the offering is expected to occur on or about August 4, 2023, subject to the satisfaction of customary closing conditions.

加利福尼亚州洛斯加托斯,2023年8月2日(GLOBE NEWSWIRE)——专注于发现和开发用于治疗危及生命的感染的新型抗感染疗法的生物制药公司Aridis Pharmicals, Inc.(场外交易代码:ARDS)今天宣布了发行1,000万股公司普通股(或代替预先融资的认股权证)和随附的认股权证的定价 00万股普通股,合并发行价为每股普通股(或预先注资的认股权证)和随附的认股权证。每份认股权证的行使价为每股0.20美元,可立即行使,并将在发行之日五周年之日终止。本次发行预计将于2023年8月4日左右结束,但须满足惯例成交条件。

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

H.C. Wainwright & Co. 担任本次发行的独家配售代理。

The gross proceeds to the Company from the offering are expected to be $2 million, before deducting the placement agent's fees and other offering expenses payable by the Company. Aridis Pharmaceuticals currently intends to use the net proceeds from the offering for working capital and general corporate purposes.

在扣除配售代理费用和公司应支付的其他发行费用之前,预计本次发行给公司的总收益为200万美元。Aridis Pharmicals目前打算将此次发行的净收益用于营运资金和一般公司用途。

The securities described above are being offered pursuant to a registration statement on Form S-1 (File No. 333-272128) originally filed with the Securities and Exchange Commission ("SEC") on May 22, 2023 and declared effective on August 1, 2023. The offering is being made only by means of a prospectus, which is part of the effective registration statement. A preliminary prospectus relating to the offering has been 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 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.

上述证券是根据S-1表格(文件编号333-272128)上的注册声明发行的,该声明最初于2023年5月22日向美国证券交易委员会(“SEC”)提交,并于2023年8月1日宣布生效。本次发行仅通过招股说明书进行,招股说明书是有效注册声明的一部分。与本次发行有关的初步招股说明书已提交给美国证券交易委员会。最终招股说明书的电子副本(如果有)可在美国证券交易委员会的网站上获得 http://www.sec.gov 也可以通过致电 (212) 856-5711 或发送电子邮件至 10022 联系位于纽约州纽约公园大道 430 号的 H.C. Wainwright & Co., LLC 获得 placements@hcwco.com

The Company also has agreed that certain existing warrants to purchase up to an aggregate of (i) 2,473,778 shares of the Company's common stock that were previously issued in August 2021, as amended, at an exercise price of $2.00 per share and (ii) 7,207,208 shares of the Company's common stock that were previously issued in October 2022, at an exercise price of $1.11 per share, will be amended effective upon the closing of the offering, such that the amended warrants will have a reduced exercise price of $0.20 per share and a termination date on the five year anniversary of the closing date of the offering.

公司还同意,某些现有认股权证,以每股2.00美元的行使价购买总额不超过 (i) 2021年8月发行的经修订的公司普通股的2473,778股,以及 (ii) 先前于2022年10月发行、行使价为每股1.11美元的7,207,208股公司普通股的认股权证,将在发行结束后进行修订,因此,修订后的认股权证的行使价将降至每股0.20美元,终止日期为五年发行截止日期的周年纪念日。

This press release shall not constitute an offer to sell or a solicitation of an offer to buy these securities, 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要约或招揽购买这些证券的要约,也不得在任何州或司法管辖区根据任何此类州或司法管辖区的证券法进行注册或获得资格之前,在任何州或司法管辖区出售这些证券,如果此类要约、招标或出售是非法的。

About Aridis Pharmaceuticals, Inc.

关于 Aridis 制药有限公司

Aridis Pharmaceuticals, Inc. discovers and develops anti-infectives to be used as first-line treatments to combat antimicrobial resistance (AMR) and viral pandemics. The Company is utilizing its proprietary ʎPEX and MabIgX technology platforms to rapidly identify rare, potent antibody-producing B-cells from patients who have successfully overcome an infection, and to rapidly manufacture mAbs for therapeutic treatment of critical infections. These mAbs are already of human origin and functionally optimized by the natural human immune system for high potency. Hence, they are already fit-for-purpose anddo not require further engineering optimization to achieve full functionality.

Aridis Pharmicals, Inc. 发现并开发了抗感染药物,可用作对抗抗微生物药物耐药性(AMR)和病毒流行的一线治疗方法。该公司正在利用其专有的 pex 和 mabiGX 技术平台,从成功克服感染的患者身上快速鉴定出稀有、强效抗体产生抗体的B细胞,并快速制造用于治疗危重感染的单克隆抗体。这些单克隆抗体已经来自人类,并经过人类天然免疫系统的功能优化,具有很高的效力。因此,它们已经适合用途,不需要进一步的工程优化即可实现全部功能。

The Company has generated multiple clinical stage mAbs targeting bacteria that cause life-threatening infections such as ventilator associated pneumonia (VAP) and hospital acquired pneumonia (HAP), in addition to preclinical stage antibacterial and antiviral mAbs. The use of mAbs as anti-infective treatments represents an innovative therapeutic approach that harnesses the human immune system to fight infections and is designed to overcome the deficiencies associated with the current standard of care, which is broad spectrum antibiotics. Such deficiencies include, but are not limited to, increasing drug resistance, short duration of efficacy, disruption of the normal flora of the human microbiome and lack of differentiation among current treatments. The mAb portfolio is complemented by a non-antibiotic novel mechanism small molecule anti-infective candidate being developed to treat lung infections in cystic fibrosis patients. The Company's pipeline is highlighted below:

除了临床前阶段的抗菌和抗病毒单抗外,该公司还生产了多个针对导致生命危险感染的细菌的临床阶段单抗体,例如呼吸机相关性肺炎(VAP)和医院获得性肺炎(HAP)。使用单克隆抗体作为抗感染治疗代表了一种利用人体免疫系统对抗感染的创新治疗方法,旨在克服与当前护理标准(即广谱抗生素)相关的缺陷。此类缺陷包括但不限于耐药性增加、疗效持续时间短、人类微生物组正常菌群的破坏以及当前治疗方法之间缺乏差异。mAb产品组合辅之以一种非抗生素的新机制小分子抗感染候选药物,用于治疗囊性纤维化患者的肺部感染。该公司的渠道如下所示:

Aridis' Pipeline

阿里迪斯的管道

AR-301 (VAP/HAP/CAP). AR-301 is a fully human IgG1 mAb currently in Phase 3 clinical development targeting gram-positive S. aureus alpha-toxin in ventilator associated pneumonia (VAP), ventilated hospital acquired pneumonia (HAP), and ventilated community acquired pneumonia (CAP) patients.

AR-301 (VAP/HAP/CAP)。AR-301 是一种全人类 IgG1 单克隆抗体,目前正处于 3 期临床开发阶段,靶向革兰氏阳性 金黄色葡萄球菌 呼吸机相关性肺炎 (VAP)、通风医院获得性肺炎 (HAP) 和通气社区获得性肺炎 (CAP) 患者中的α-毒素。

AR-501 (cystic fibrosis). AR-501 is an inhaled formulation of gallium citrate with broad-spectrum anti-infective activity being developed to treat chronic lung infections in cystic fibrosis patients. This program is currently in a Phase 2a clinical study in CF patients.

AR-501 (囊性纤维化)。AR-501 是一种具有广谱抗感染活性的柠檬酸镓吸入制剂,用于治疗囊性纤维化患者的慢性肺部感染。该项目目前正处于针对 CF 患者的2a期临床研究中。

AR-320 (VAP). AR-320 is a fully human mAb targeting S. aureus alpha-toxin for prevention of VAP. Statistically significant Phase 2 data in the target population of those ≤ 65 years of age was published in the September 2021 Lancet Infectious Diseases journal. The Company has completed discussions with the EMA and FDA on study design and recently launched the Phase 3 study.

AR-320 (VAP)。AR-320 是一种全人类 mAB 靶向 金黄色葡萄球菌 用于预防 VAP 的 α-毒素。2021 年 9 月《柳叶刀传染病》杂志上发布了目标人群中 65 岁以下人群的第 2 阶段数据,具有统计学意义。该公司已经完成了与EMA和FDA关于研究设计的讨论,最近启动了第三阶段研究。

AR-701 (COVID-19). AR-701 is a cocktail of fully human mAbs discovered from convalescent COVID-19 patients that target multiple sites on the spike proteins of the SARS-CoV-2 virus.

AR-701 (新冠肺炎)。AR-701 是一种从康复期的 COVID-19 患者身上发现的全人类 mAB 混合物,靶向 SARS-CoV-2 病毒刺突蛋白的多个位点。

AR-101 (HAP). AR-101 is a fully human IgM mAb in Phase 2 clinical development targeting Pseudomonas aeruginosa liposaccharides serotype O11, which accounts for approximately 22% of all P. aeruginosa HAP cases worldwide. This program is licensed to the Serum Institute of India and Shenzhen Arimab.

AR-101 (哈普)。AR-101 是一种全人类 IgM 单抗体,正处于 2 期临床开发阶段 铜绿假单胞菌 脂糖血清型 O11,约占所有脂糖的 22% 铜绿假单胞菌 全球范围内的 HAP 病例。该项目已获得印度血清研究所和深圳Arimab的许可。

AR-201 (RSV infection). AR-201 is a fully human IgG1 mAb directed against the F-protein of diverse clinical isolates of respiratory syncytial virus (RSV). This program is licensed exclusively to the Serum Institute of India.

AR-201 (呼吸道合胞病毒感染)。AR-201 是一种针对呼吸道合胞病毒 (RSV) 多种临床分离株的 F 蛋白的全人类 IgG1 单抗。该程序由印度血清研究所独家授权。

AR-401 (blood stream infections). AR-401 is a fully human mAb preclinical program aimed at treating infections caused by gram-negative Acinetobacter baumannii.

AR-401 (血液感染)。AR-401 是一项全人类 mAB 临床前项目,旨在治疗革兰氏阴性引起的感染 鲍曼不动杆菌

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