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Genenta Announces Pricing of $15.0 Million Registered Direct Offering of American Depositary Shares Milan, Italy and New York, USA

Key Takeaway: Genenta Science announced a registered direct offering of 4,285,715 American Depositary Shares at $3.50 per share, raising approximately $15 million. The funds will be allocated for working capital and corporate purposes, supporting ongoing clinical trials, including for their proprietary therapy, Temferon. The offering is set to close by October 28, 2025, pending customary closing conditions. However, the company notes potential risks associated with these forward-looking statements and the investigational status of their therapies.

Market Sentiment Analysis

POSITIVE FACTORS

  • Genenta has successfully raised $15 million through a direct offering.
  • The proceeds will support working capital and ongoing clinical trials.
  • The company is pioneering innovative therapies in immuno-oncology.

CONCERNS & RISKS

  • Forward-looking statements indicate inherent risks and uncertainties.
  • The company has not yet received approval for its investigational product Temferon.

Full Press Release Details

Announces Pricing of $15.0 Million Registered Direct Offering of American Depositary Shares
Italy and New York, USA, October 26, 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 $3.50 per ADS, for gross proceeds of approximately $15.0 million, before deducting
placement agent fees and other estimated offering expenses. All of the securities in the offering were sold by Genenta, and no warrants
or other derivative securities were issued in connection with this offering.
Group LLC is acting as lead placement agent for the offering, and Rodman & Renshaw LLC is acting as co-placement agent for the offering.
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.
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.
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.
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.
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.
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Frequently Asked Questions

What is Genenta Science's recent offering amount?

Genenta Science announced a $15.0 million registered direct offering.

What is the price per American Depositary Share (ADS)?

Each American Depositary Share is priced at $3.50.

Who acted as the placement agents for the offering?

Group LLC is the lead agent and Rodman & Renshaw LLC is the co-agent.

When is the expected closing date for the offering?

The offering is expected to close on or about October 28, 2025.

What will the proceeds be used for?

Net proceeds will be used for working capital and general corporate purposes.

Last updated: Oct 26, 2025