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Genenta Advances Transformation into Saentra Forge, Strengthens ATC Governance and Expands Strategic Industrial Consolidation Platform

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Genenta Science (Nasdaq: GNTA), transforming into Saentra Forge (Nasdaq: SAEN), announced appointment of Paolo Salvato to the Board of ATC, marking its first entry into defense manufacturing, and confirmed ongoing evaluation of majority-control acquisitions in regulated national-security sectors. Nature Medicine accepted a manuscript reporting key clinical findings from the company’s Glioblastoma multiforme trial, with publication expected in the coming weeks.

Management said it is prioritizing profitable, majority-controlled industrial scale-ups and evaluating biotech partnerships to reduce capital needs for registrational studies, while retaining flexibility to access U.S. public markets subject to market and regulatory conditions.

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Positive

  • Nature Medicine accepted GBM clinical manuscript for publication
  • Appointed Paolo Salvato to ATC board to strengthen defense governance
  • Targeting profitable, majority-controlled industrial scale-ups for consolidation
  • Access to Nasdaq listing could provide U.S. public capital market flexibility

Negative

  • Biotech registrational plans require substantial capital and increase risk exposure
  • Accessing U.S. public markets is subject to market conditions and regulation

Market Reality Check

Price: $0.9601 Vol: Volume 50,720 vs 20-day a...
low vol
$0.9601 Last Close
Volume Volume 50,720 vs 20-day avg 182,173 (relative volume 0.28) shows subdued trading ahead of this news. low
Technical Shares at 0.9601 are trading below the 200-day MA of 2.77 and sit 90.4% under the 52-week high of 10.

Peers on Argus

Peer biotech moves are mixed: ATNM +0.88%, INMB -4.29%, VTVT +3.47%, PDSB -0.36%...

Peer biotech moves are mixed: ATNM +0.88%, INMB -4.29%, VTVT +3.47%, PDSB -0.36%, PYPD -0.71%. With GNTA down 3.99%, the pattern suggests stock-specific dynamics rather than a coordinated sector move.

Historical Context

5 past events · Latest: 2026-01-27 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
2026-01-27 Strategic transformation Positive +18.5% Announced shift to Saentra Forge industrial consolidator and ATC acquisition plan.
2025-12-19 Insider ownership update Positive -2.0% CEO disclosed sizable stake and open-market ADS purchases with no reported sales.
2025-11-24 GBM trial update Positive +6.0% Reported improved long-term survival trends and supportive immune findings in GBM trial.
2025-10-26 Equity offering Negative -46.5% Priced $15.0M registered direct ADS offering at $3.50 for corporate purposes.
2025-10-24 Strategic partnership Positive +92.0% Expanded LVV plasmid DNA collaboration with Anemocyte for off-the-shelf platform.
Pattern Detected

GNTA’s past five news events show reactions mostly aligned with the underlying news tone, with only one notable divergence on insider-ownership disclosure.

Recent Company History

Over the last several months, GNTA has moved from a Temferon-focused biotech toward a broader industrial consolidator strategy. On Jan 27, 2026 it outlined the Saentra Forge transformation and staged ATC acquisition, which saw a +18.46% reaction. Earlier, GBM clinical data on Nov 24, 2025 and an LVV plasmid DNA partnership on Oct 24, 2025 were followed by gains of 5.95% and 91.95%, respectively. A $15.0M registered direct offering on Oct 26, 2025 led to a -46.45% drop, underscoring sensitivity to equity financing. Today’s update reinforces the same transformation and GBM program validation.

Market Pulse Summary

This announcement advances GNTA’s transition into Saentra Forge while reinforcing governance at ATC ...
Analysis

This announcement advances GNTA’s transition into Saentra Forge while reinforcing governance at ATC and highlighting Nature Medicine’s acceptance of GBM clinical data. It builds on earlier disclosures about the industrial consolidation strategy and prior GBM survival findings. Key factors to watch include progress on majority-control acquisitions in regulated national-security sectors, terms of any biotech partnering deals, and how future capital allocation balances industrial roll-ups with legacy cell-therapy assets. The Nature Medicine publication timing and content will also be important validation milestones.

Key Terms

glioblastoma multiforme (GBM), EBITDA, registrational studies
3 terms
glioblastoma multiforme (GBM) medical
"a manuscript describing key clinical findings from its Glioblastoma Multiforme (GBM) trial"
Glioblastoma multiforme (GBM) is an aggressive, fast-growing form of brain cancer that spreads into surrounding tissue and is difficult to remove or cure. Its poor patient outlook and lack of effective standard treatments make GBM a high-priority target for new drugs and medical devices, so clinical trial results, regulatory decisions, or scientific breakthroughs can meaningfully affect companies involved in research and the potential market for effective therapies—like clearing a large patch of persistent weeds that others have struggled to remove.
EBITDA financial
"We are focused on acquiring profitable industrial scale-ups with positive EBITDA."
EBITDA stands for earnings before interest, taxes, depreciation, and amortization. It measures a company's profitability by focusing on the money it makes from its core operations, ignoring expenses like taxes and accounting adjustments. Investors use EBITDA to compare how well different companies are performing financially, as it provides a clearer picture of operational success without the influence of financial structure or accounting choices.
registrational studies regulatory
"Pursuing combination or registrational studies independently would require substantial additional capital"
Clinical trials run specifically to provide the evidence regulators require for approval of a new drug, device, or treatment. They are the final, rigorous tests—like a product’s “final exam” or blueprint review—that determine whether a therapy can legally be marketed, so their outcomes directly affect a company’s ability to generate revenue, timelines to market and overall investment risk.

AI-generated analysis. Not financial advice.

Nature Medicine Accepts Manuscript Highlighting Clinical Results from the Company’s Glioblastoma Trial

MILAN, Feb. 27, 2026 (GLOBE NEWSWIRE) -- Genenta Science S.p.A. (Nasdaq: GNTA) in transformation to Saentra Forge (Nasdaq: SAEN), a strategic industrial consolidator focused on biotech, defense, aerospace, and national-security-related technologies, today announced the appointment of Paolo Salvato to the Board of Directors of ATC, a manufacturer of tactical defense systems representing the Company’s initial entry into defense technology manufacturing. The Company also provided an update on its ongoing evaluation of majority-control acquisition opportunities in regulated national-security sectors.

Mr. Salvato previously served as Chief Executive Officer of Fiocchi Munizioni S.p.A. (CSG Group), where he led operational strengthening, international growth initiatives, and strategic positioning within the global defense ecosystem. He brings more than two decades of experience across defense industrial operations, with expertise spanning manufacturing execution, export markets, supply chain management, and regulatory compliance. Prior to Fiocchi Munizioni, he served as Chief Executive Officer of Thales Italia, and he held senior leadership roles at Leonardo S.p.A., deepening his experience across the European defense and aerospace ecosystem.

As part of its broader strategic transition into Saentra Forge, the Company continues to evaluate selected acquisition opportunities in the national-security regulated sectors1, with the object of building a next-generation strategic industrial consolidator of tech and scale-up companies. Management, now supported by Paolo Salvato, is reviewing potential targets that align with its capital allocation framework, focusing on profitable, majority-controlled, privately-held industrial businesses.

Acquired companies will be able to benefit from additional financial flexibility to support disciplined growth, as the Company may access the U.S. public capital markets through the Company’s Nasdaq listing, subject to market conditions and applicable regulatory requirements. This is further complemented by the strategic network of Fondazione Praexidia2, intended to support the development of institutional relationships and industrial partnerships.

On the biotech side, the Company today announced that Nature Medicine has accepted for publication a manuscript describing key clinical findings from its Glioblastoma Multiforme (GBM) trial. The publication is expected in the coming weeks, subject to the journal’s schedule, and represents an important validation of the Company’s scientific and clinical work.

Pierluigi Paracchi, Chief Executive Officer, commented, “Our transformation reflects a deliberate response to evolving market dynamics and long-term industrial opportunities. We believe advanced biotechnology and defense-related technologies increasingly intersect in areas of national resilience and strategic industrial capability, as evidenced by initiatives such as the NATO Innovation Fund and investment strategies of frontier-focused firms.”

“Our biotech program has reached clinical maturity, where a strategic partnership represents the most efficient path to advance development and maximize its long-term potential. Pursuing combination or registrational studies independently would require substantial additional capital and increase risk exposure. We are therefore evaluating potential partnership opportunities that could provide development expertise, shared risk, and capital support.”

“In parallel, we maintain financial resources to execute our industrial aggregation strategy. We are focused on acquiring profitable industrial scale-ups with positive EBITDA. As a publicly listed company, we believe we are well positioned to acquire privately held businesses at private market valuations and integrate them within a transparent, listed platform built for operational scale and long-term value creation.”

About: Genenta Science (Nasdaq: GNTA), which will be renamed as Saentra Forge (Nasdaq: SAEN, pending effectiveness), will be a next-generation strategic consolidator focused on privately held specialized companies operating in Italian national security regulated sectors, with activities spanning cybersecurity, defense, aerospace, and biotechnology/biosecurity.

Non-GAAP Information. This release includes EBITDA, which is a non-GAAP financial measure. EBITDA is defined as net loss adjusted to exclude interest income, income tax expense, and depreciation and amortization. This non-GAAP measure is not in accordance with, or an alternative for, measures prepared in accordance with generally accepted accounting principles (GAAP) and may be different from non-GAAP measures used by other companies. In addition, this non-GAAP measure is not based on any comprehensive set of accounting rules or principles. Genenta believes that this non-GAAP financial measure, when considered together with financial information prepared in accordance with GAAP, can enhance investors’ and analysts’ ability to meaningfully compare its results from period to period and to forward-looking guidance, and to identify operating trends in its business. However, non-GAAP information is not superior to financial measures calculated in accordance with GAAP, is presented for supplemental informational purposes only, has limitations as an analytical tool, and should not be considered in isolation or as a substitute for financial information presented in accordance with GAAP.

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 transition to Saentra Forge, the expansion to a sovereign-aligned industrial consolidator, the legal proceedings with ENEA Tech, the funding provided by the recently acquired Mandatory Convertible Bond, the Phase 1/2a clinical trial for newly diagnosed GBM patients with uMGMT-GBM or any related studies, as well as Genenta’s ability to establish partnerships and 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, and Genenta's material disclosures on Form 6-K dated January 26, 2026, both 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


1 No definitive agreements have been executed with respect to any such potential transactions. There can be no assurance that any transaction will be completed, nor as to the timing or terms of any potential transaction.
2 www.fondazionepraexidia.org


FAQ

What did Genenta (GNTA) announce about its transformation to Saentra Forge (SAEN) on February 27, 2026?

Genenta said it is transforming into Saentra Forge to become a strategic industrial consolidator. According to the company, the plan targets biotech, defense, aerospace, and national-security-related technologies and will pursue majority-control acquisitions aligned with its capital allocation framework.

What is the significance of Paolo Salvato joining ATC’s board for GNTA/SAEN investors?

His appointment strengthens ATC governance and defense manufacturing expertise. According to the company, Salvato brings over two decades of defense industry leadership and operational experience, supporting the company’s initial entry into regulated defense technology manufacturing.

What did Genenta announce about its Glioblastoma trial publication on February 27, 2026?

Nature Medicine accepted the company’s manuscript reporting key GBM clinical findings, with publication expected in coming weeks. According to the company, this represents an important validation of its scientific and clinical work for the biotech program.

How is GNTA planning to finance acquisitions and biotech development under Saentra Forge?

The company may use its Nasdaq listing to access U.S. public capital markets for financial flexibility. According to the company, it will focus on profitable, privately held businesses and pursue biotech partnerships to share development risk and capital needs.

Will Genenta pursue acquisitions in national-security regulated sectors immediately?

Management is actively evaluating majority-control acquisition opportunities but has not announced closed transactions. According to the company, target selection focuses on profitable industrial scale-ups that fit its capital allocation framework and regulatory requirements.
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