Genenta and Anemocyte announce a collaboration for the manufacturing of starting materials for cutting-edge cell-based therapies
May 07 2025 - 7:00AM
Genenta Science (Nasdaq: GNTA), a pioneer in immuno-oncology and a
leader in cell-based therapeutics, today announced a collaboration
with Anemocyte, a leading Biotech Manufacturing Organization (BMO)
based in Italy. This strategic partnership marks a major milestone,
encompassing the successful production of critical starting
materials, including the establishment of Cell Banks and the
manufacturing of Plasmids for viral vector production.
This collaboration represents a pivotal step in
the advancement of immuno-oncology therapies, highlighting the
powerful synergy between Genenta's innovative platform and
Anemocyte's proven expertise in the production of high-quality
starting materials.
"Thanks to Anemocyte, Genenta has achieved
significant milestones in the progression of its clinical trials.
The expertise and knowledge of Anemocyte’s team have been
instrumental throughout the entire manufacturing process of these
critical starting materials," stated Carlo Russo, M.D., Chief
Medical Officer & Head of Development of Genenta Science.
"Further manufacturing steps confirmed our expectations with
Anemocyte’s plasmid DNA in the production of high-quality
therapeutic products. Such results confirmed the role of Anemocyte
as a top-quality, cost-effective, and reliable partner."
"Genenta's status as the first Italian company
listed on Nasdaq is a testament to its innovation and leadership in
the immuno-oncology space. We are immensely proud of this
collaboration with Genenta supporting its pioneering product and
technology, facilitating further progress in the next phase of
trials," expressed Marco Ferrari, CEO of Anemocyte. "Genenta
symbolizes the concerted efforts of the Italian industry and
academia to accelerate advancements in the Cell and Gene
therapeutic field. Moreover, this collaboration confirms the
direction Anemocyte has taken as future steps which have been built
around pillars of flexibility, quality, and sustainability."
About Anemocyte:Anemocyte is a
Biotech Manufacturing Organization (BMO) based in Italy, offering
comprehensive development and manufacturing services and providing
innovative solutions from R&D to GMP. Specialized in the
development and production of pDNA and mRNA, Anemocyte brings over
25 years of expertise in manufacturing innovative therapies and
related starting materials.For more information, visit
www.anemocyte.com.
About GenentaGenenta (Nasdaq:
GNTA) is a clinical-stage immuno-oncology company developing a
proprietary hematopoietic stem cell 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
StatementsStatements 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 MediaTiziana Pollio, Mobile: +39 348 23 15
143Email: tiziana.pollio@genenta.com
Anemocyte MediaTelephone +39
0299372311Email: media@anemocyte.comwww.anemocyte.com
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