Genenta Showcases Strategic Vision at Premier Biotech Forum in Qatar
Rhea-AI Summary
Genenta Science (Nasdaq: GNTA) announced its upcoming presentation at the 'Montalcini Global Biotech Tour' in Doha, Qatar on April 17th, 2025. The presentation follows two significant financial developments:
1. A €20 million ($22.7 million) strategic financing through a Mandatory Convertible Bond to ENEA Tech and Biomedical (ETB), aimed at advancing Temferon™ in metastatic Renal Cell Cancer (mRCC)
2. An additional €3.0 million ($3.2 million) raised via an at-the-market (ATM) facility
The event will be hosted by Qatar's Minister of State for Foreign Trade Affairs and Italy's Minister of Health, featuring presentations from key stakeholders including Qatar Research, Development and Innovation Council (QRDI) and potential meetings with Qatar Investment Authority (QIA), which manages over $475 billion in assets.
Positive
- Secured €20 million ($22.7 million) strategic financing through Mandatory Convertible Bond
- Additional €3.0 million ($3.2 million) raised via ATM facility
- Potential partnership opportunity with Qatar Investment Authority ($475B AUM)
Negative
- None.
Insights
Genenta's securing of
The use of a mandatory convertible structure suggests future equity dilution for existing shareholders, though this approach allows Genenta to secure significant capital without immediately flooding the market with new shares. The additional fundraising through the ATM facility indicates management is actively shoring up the company's financial position through multiple channels.
The timing of this capital raise alongside the company's participation in Qatar's biotech forum is strategically significant. By presenting to potential Middle Eastern investors including representatives from Qatar Investment Authority's
MILAN and NEW YORK, April 15, 2025 (GLOBE NEWSWIRE) -- Pierluigi Paracchi, CEO Genenta Science (Nasdaq: GNTA), a pioneer in immuno-oncology and a leader in cell-based therapeutics, will present at “Montalcini Global Biotech Tour” in Doha, Qatar on April 17th, 2025 at the Sheikh Fahad bin Jassim Al Thani theatre, Ministry of Commerce and Industry (MOCI) Building.
Following the announcement of a
Paracchi, who also serves as Moderator of the National Working Table for the Internationalization of the Italian Biotech sector (NWTIB) — a strategic initiative launched by Italian Deputy Prime Minister and Minister of Foreign Affairs Antonio Tajani — will speak during the session dedicated to the “Italian Biotech & Lifesciences Ecosystem,” which will also feature Massimo Carnelos, Head of the Office for Technological Innovation and Startups at the Italian Ministry of Foreign Affairs, and Mario Scuderi, Senior Partner at CDP Venture Capital. CDP VC is a long-standing investor in Genenta, having participated in the company’s IPO on Nasdaq in 2021.
The program includes presentations by key institutional stakeholders such as Qatar Research, Development and Innovation Council (QRDI), represented by Dr. Sara A. Abdulla, Senior Research Program Manager, and concludes with bilateral meetings featuring representatives of the Qatar Investment Authority (QIA) — the country’s sovereign wealth fund managing over
Note: The information provided herein regarding the Mandatory Convertible Bond is a summary and does not purport to be comprehensive. The full terms and conditions of the Mandatory Convertible Bond are set forth in the official subscription agreement by and between Genenta and ETB and relevant bond regulations, which are detailed and govern the issuance of the Mandatory Convertible Bond. Investors are encouraged to refer to the full documentation. The complete documentation with respect to the Mandatory Convertible Bond is available in the Company’s Form 6-K filing with the SEC filed concurrently with this press release and on the Company's website at www.genenta.com.
Note: For further details on the ATM facility, investors are encouraged to consult the Company’s Form 6-K filed with the SEC on March 19, 2025 and available on Genenta’s website at www.genenta.com
About Genenta
Genenta (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 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 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 in Q4 2024 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 funding to be provided by the Mandatory Convertible Bond, the completion and timing of Genenta's ongoing 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, 2023 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 Media
Tiziana Pollio, Mobile: +39 348 23 15 143
e-mail: tiziana.pollio@genenta.com