Genenta Welcomes New Directors John L. Cantello, Lauren H. Chung, Armon R. Sharei, and Todd Wider
May 06 2024 - 5:25AM
Genenta Science (NASDAQ: GNTA), a clinical-stage immuno-oncology
company developing a cell-based platform harnessing the power of
hematopoietic stem cells to provide durable and safe treatments for
solid tumors, announces that it held its Ordinary and Extraordinary
Shareholders' Meeting on May 2, 2024. At the Ordinary and
Extraordinary Shareholders' Meeting, the Company's shareholders
approved the appointment of five directors to the Company's Board
of Directors, effective as of May 2, 2024, including four new
members. The new members of the Board include:
John L.
Cantello, Ph.D., Lauren H. Chung, Ph.D., Armon R. Sharei, Ph.D. and
Todd Wider, M.D., and
Pierluigi Paracchi,
Chief Executive Officer, will continue to serve on the Board as
Chairman.
"When Luigi Naldini, Ph.D., M.D., and I
co-founded Genenta, we always aspired to involve leading figures in
the biotech sector. This Board is fantastic. Our new directors will
support Genenta as we aim to consolidate the important results we
have achieved so far and to expand the potential impact of our cell
therapy for treating tumors," said Pierluigi
Paracchi.
The Company extends its thanks to the former
members of its Board for their significant contributions throughout
their service.
John L. Cantello, Ph.D. John is
an independent advisor to the biopharma industry with over 20 years
of experience. John served as the Former VP and Head of Business
Development, Oncology Therapy Area at GlaxoSmithKline and VP and
Head of BD, Respiratory & Immune Diseases at AstraZeneca. John
has led teams accountable for assessing, valuing, and transacting
M&A, pipeline & commercial asset deals covering oncology,
respiratory, inflammation, metabolic, and rare diseases. He has a
track record of closing deals (transacting >$30B in deal value)
representing primary care, specialty care, and rare diseases.
Lauren H. Chung, Ph.D.Lauren
has over 20 years of operating experience spearheading agile
investment management strategies and tactical asset allocation in
the healthcare industry. As the founder and CEO of Minleigh LLC, a
healthcare focused strategic advisory firm, Lauren has advised
leadership, boards, and investment firms on global strategic plans,
M&A, integration, and compliance. Previously, Lauren co-founded
Tokum Capital Management, a global institutional healthcare fund,
and successfully managed its merger with Perella Weinberg Partners.
Lauren serves on public and private company boards. She has a Ph.D.
in Biomedical Sciences from Columbia University Vagelos College of
Physicians and Surgeons, an M.B.A. from Columbia Business School,
and a B.A. in Biochemistry and Economics with Honors from Wellesley
College.
Armon R. Sharei, Ph.D.Armon is
the founder and CEO of Portal Bio and formerly the CEO and founder
of SQZ Biotechnologies, where he led the company from
invention to post-IPO with over $300 million in equity financing, a
$1 billion collaboration with Roche, and three clinical trials. He
graduated from Stanford University, and received his Ph.D. at
Massachusetts Institute of Technology and his Post-Doctoral at
Harvard Medical School.
Todd Wider, M.D.Todd has served
as a consultant to numerous entities in the biotechnology space. He
is a co-founder and Board member of Xanadu Bio and prior Executive
Chairman of Emendo Biotetherapeutics, Board member of Abeona
Therapeutics and Arya Science Acquisition Corp IV (Nasdaq: ARYD).
Todd is an active, honorary member of the medical staff of Mount
Sinai Hospital in New York City. He received his M.D. from Columbia
University's Vagelos College of Physicians and Surgeons where he
was Rudin Fellow, and an A.B., with high honors and Phi Beta Kappa,
from Princeton University. Todd is also a principal in Wider Film
Projects, a documentary film company focused on producing films
with sociopolitical resonance that have won Academy, Emmy and
Peabody Awards.
Additional information related to the Genenta
shareholders’ meeting are reported on a Form 6-K filed with the
U.S. Securities and Exchange Commission and made available on
the Company’s website (www.genenta.com).
About Genenta and
TemferonGenenta (www.genenta.com) is a clinical-stage
biotechnology company engaged in the development of a proprietary
hematopoietic stem cell therapy for the treatment of a variety of
solid tumor cancers. Temferon™ is based on ex-vivo gene transfer
into autologous Tie2+ hematopoietic stem/progenitor cells (HSPCs)
to deliver immunomodulatory molecules directly via
tumor-infiltrating monocytes/macrophages (Tie2 Expressing Monocytes
- TEMs). Temferon, which is under investigation in a phase 1/2a
clinical trial in newly diagnosed Glioblastoma Multiforme patients
who have an unmethylated MGMT gene promoter (uMGMT-GBM), is
designed to reach solid tumors, induce a durable immune response
not restricted to pre-selected tumor antigens nor type, and avoid
systemic toxicity, which are some of the main unresolved challenges
in immuno-oncology.
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 completion and timing of the phase 1/2a
clinical trial or any studies relating to the treatment of
glioblastoma multiforme patients who have an unmethylated MGMT gene
promoter (uMGMT-GBM). 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, 2022 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.
Genenta Media: Tiziana Pollio, mobile +39 348 23 15 143
tiziana.pollio@genenta.com
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