Genenta Announces Pricing of $15.0 Million Registered Direct Offering of American Depositary Shares
Genenta Science (Nasdaq: GNTA) announced a registered direct offering to sell 4,285,715 ADSs at $3.50 per ADS for gross proceeds of approximately $15.0 million, before fees and expenses. Maxim Group is lead placement agent and Rodman & Renshaw is co-placement agent. Genenta intends to use net proceeds for working capital and general corporate purposes. The offering is expected to close on or about October 28, 2025, subject to customary closing conditions and a prospectus supplement to be filed under its effective Form F-3 registration.
Genenta Science (Nasdaq: GNTA) ha annunciato un'offerta diretta registrata per vendere 4.285.715 ADS a $3,50 per ADS per ottenere proventi lordi di circa $15,0 milioni, prima delle commissioni e delle spese. Maxim Group è l'agente principale di collocamento e Rodman & Renshaw è co-collocatore. Genenta intende utilizzare i proventi netti per capitale circolante e scopi aziendali generali. Si prevede che l'offerta si chiuda indicativamente entro il 28 ottobre 2025, soggetta alle consuete condizioni di chiusura e a un supplemento di prospetto da depositare ai sensi del suo Form F-3 registrato efficacemente.
Genenta Science (Nasdaq: GNTA) anunció una oferta directa registrada para vender 4,285,715 ADS a $3.50 por ADS para ingresos brutos de aproximadamente $15.0 millones, antes de comisiones y gastos. Maxim Group es el agente principal de colocación y Rodman & Renshaw es el coagente de colocación. Genenta tiene la intención de usar los ingresos netos para capital de trabajo y fines corporativos generales. Se espera que la oferta cierre aproximadamente el 28 de octubre de 2025, sujeto a condiciones de cierre habituales y a un suplemento de prospecto que se presentará en su registro Form F-3 vigente.
Genenta Science (나스닥: GNTA)는 4,285,715 ADS를 $3.50/ADS의 가격으로 등록된 직접 공모를 통해 매각하여 총 약 $15,000,000의 매출을 얻겠다고 발표했습니다. 수수료와 비용 차감 전. Maxim Group은 주간 배정의 선두 에이전트이고 Rodman & Renshaw가 공동 배정 에이전트입니다. Genenta는 순매출금을 운전자본 및 일반 기업 목적용으로 사용할 예정입니다. 이 공모는 관례적 마감 조건 및 시행 Form F-3 등록의 효력 있는 보충설명서가 제출될 예정인 2025년 10월 28일 경에 마감될 것으로 예상됩니다.
Genenta Science (Nasdaq : GNTA) a annoncé une offre directe enregistrée visant à vendre 4 285 715 ADS à 3,50 $ par ADS pour un produit brut d'environ 15,0 millions de dollars, frais et dépenses avant. Maxim Group est l'agent principal de placement et Rodman & Renshaw est l'agent de placement associé. Genenta a l'intention d'utiliser le produit net pour fonds de roulement et usages généraux de l'entreprise. L'offre devrait être clôturée aux alentours du 28 octobre 2025, sous réserve des conditions de clôture habituelles et d'un supplément de prospectus à déposer sous son enregistrement Form F-3 en vigueur.
Genenta Science (Nasdaq: GNTA) kündigte eine registrierte Direct-Offering zum Verkauf von 4.285.715 ADS zu 3,50 $ pro ADS an für Bruttoerlöse von ca. 15,0 Mio. USD, vor Gebühren und Aufwendungen. Maxim Group ist Lead Placement Agent und Rodman & Renshaw ist Co-Placement Agent. Genenta beabsichtigt, Nettoprovisionen für Working Capital und allgemeine Unternehmenszwecke zu verwenden. Das Angebot wird voraussichtlich am oder um den 28. Oktober 2025 geschlossen, vorbehaltlich üblicher Abschlussbedingungen und eines Prospektzusatzes, der unter dem gültigen Form F-3-Registrierungsverfahren eingereicht wird.
Genenta Science (ناسداك: GNTA) أعلنت عن عرض مباشر مسجل لبيع 4,285,715 ADS بسعر $3.50 لكل ADS لتحقيق عوائد إجمالية تقارب $15.0 مليون، قبل الرسوم والنفقات. Maxim Group هي الوكيل الرئيسي للطرح و Rodman & Renshaw هي الوكيل المشترك. تعتزم Genenta استخدام العائدات المتبقية لـ رأس المال العامل والأغراض العامة للشركة. من المتوقع إغلاق العرض في أو حوالي 28 أكتوبر 2025، مع مراعاة الشروط المعتادة للإغلاق ومُلحق نشرة الإصدار الذي سيتم تقديمه بموجب تسجيل Form F-3 الفعال.
Genenta Science(纳斯达克:GNTA)宣布进行一项注册直接发行,拟以每股ADS 3.50美元出售4,285,715股ADS,毛收入约为1500万美元,未扣除费用和支出。 Maxim Group 为主承销商,Rodman & Renshaw 为联席承销商。Genenta 计划将净收益用于营运资金和公司一般用途。该发行预计在大约2025年10月28日前后完成,前提是符合常规交割条件,并将就其有效的F-3注册提交招股说明书补充文件。
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Insights
Genenta priced a $15.0 million registered direct ADS offering to fund working capital; closing expected on or about 
Genenta agreed to sell 4,285,715 ADSs at 
The immediate business effect is increased near-term liquidity that should support operations and ongoing clinical programs mentioned, including the completed Phase 1 GBM cohort and the initiated Phase 1/2a metastatic RCC study. Key dependencies and risks include successful closing on or about 
MILAN and NEW YORK, Oct.  27, 2025  (GLOBE NEWSWIRE) -- Genenta Science (Nasdaq: GNTA), a pioneer in immuno-oncology, today announced that it has entered into a securities purchase agreement with institutional investors to purchase 4,285,715 American Depositary Shares ("ADSs") at an offering price of 
Maxim Group LLC is acting as lead placement agent for the offering, and Rodman & Renshaw LLC is acting as co-placement agent for the offering.
Genenta intends to use the net proceeds from the offering for working capital and general corporate purposes. The offering is expected to close on or about October 28, 2025, subject to the satisfaction of customary closing conditions.
The securities described above are being offered pursuant to a shelf registration statement on Form F-3 (File No. 333-271901) previously filed with the U.S. Securities and Exchange Commission (“SEC”) and declared effective on May 24, 2023. A prospectus supplement relating to the securities to be issued in the offering will be filed by the Company with the SEC. When available, copies of the prospectus supplement relating to the offering, together with the accompanying prospectus, can be obtained at the SEC's website at www.sec.gov or by contacting Maxim Group LLC, at 300 Park Avenue, 16th Floor, New York, NY 10022, Attention: Syndicate Department, or via email at syndicate@maximgrp.com or by telephone at (212) 895-3745., or from Rodman & Renshaw LLC at 600 Lexington Avenue, 32nd Floor, New York, NY 10022, by telephone at (212) 540-4414, or by email at info@rodm.com.
This press release shall not constitute an offer to sell or the 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 registration or qualification under the securities laws of any such state or jurisdiction.
About Genenta Science 
Genenta Science (Nasdaq: GNTA) is a clinical stage immuno-oncology company developing a proprietary hematopoietic stem cells therapy for the treatment of a variety of solid tumor cancers. Genenta’s first in class product candidate is Temferon™, which is designed to allow the expression of immune-therapeutic payloads within the tumor microenvironment by bone marrow derived myeloid cells and enable a durable and targeted response. Genenta has completed the Phase 1 trial for newly diagnosed Glioblastoma Multiforme (GBM) patients with an unmethylated MGMT gene promoter, which suggests the potential reprogramming of the tumor microenvironment and inhibiting of myeloid induced tolerance, while allowing the induction of T cell responses, potentially breaking immune tolerance. Genenta has initiated a Phase 1/2a metastatic Renal Cell Carcinoma study that will also include a combination with immune checkpoint inhibitors. Genenta’s treatments are designed as one-time monotherapies, but with the additional potential, when used in combination, to significantly enhance the efficacy of other approved therapeutics.
Forward-Looking Statements 
Statements in this press release contain “forward-looking statements,” within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “suggest,” “target,” “aim,” “should,” "will,” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on Genenta’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict, including risks related to the expected completion, timing and size of the offering, Genenta's intended use of the proceeds from the offering, the funding provided by the recently acquired Mandatory Convertible Bond, the completion and timing of Genenta's ongoing Phase 1/2a clinical trial for newly diagnosed GBM patients with uMGMT-GBM, its clinical trial for metastatic RCC or any related studies, as well as Genenta’s ability to fund its research and development plans. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully in the section titled “Risk Factors” in Genenta's Annual Report on Form 20-F for the year ended December 31, 2024 filed with the Securities and Exchange Commission. Forward-looking statements contained in this announcement are made as of the date of this announcement, and Genenta undertakes no duty to update such information except as required under applicable law. This press release discusses product candidates that are under preclinical or clinical evaluation and that have not yet been approved for marketing by the U.S. Food and Drug Administration or any other regulatory authority. Until finalized in a clinical study report, clinical trial data presented herein remain subject to adjustment as a result of clinical site audits and other review processes. No representation is made as to the safety or effectiveness of these product candidates or the use for which such product candidates are being studied. Temferon™ is an investigational product candidate for which the effectiveness and safety have not been established. In addition, Temferon™ is not approved for use in any jurisdiction.
Genenta Science Media 
Tiziana Pollio, Mobile: +39 348 23 15 143 
E-mail: tiziana.pollio@genenta.com
 
    
      
  
 
             
             
             
             
             
             
             
         
         
         
        