Nkarta Adds Experienced Leader in Autoimmune R&D, George Vratsanos, M.D., FACR, to Board of Directors
14 June 2024 - 6:01AM
Nkarta, Inc. (Nasdaq: NKTX), a clinical-stage biopharmaceutical
company developing engineered natural killer (NK) cell therapies
today announced that translational immunology expert George
Vratsanos, M.D., FACR, is joining its board of directors.
Dr. Vratsanos currently serves as Chief Medical Officer and Head
of R&D for Jnana Therapeutics where he oversees the company’s
R&D work to treat phenylketonuria and a broad range of
immune-mediated diseases.
He previously held R&D leadership roles as Senior Vice
President of Translational Science and Medicine, Immunology at
Janssen Pharmaceuticals, Executive Global Program Head of the
Immunology and Dermatology Franchise at Novartis, as well as a
Translational Medicine Leader at Roche and a Group Director at
Bristol Meyers Squibb.
“George is an accomplished physician-scientist whose R&D
leadership experience spans multiple autoimmune diseases areas and
the successful development of approved therapies such as
Orencia® and Cosentyx®,” said Paul J. Hastings, President and
CEO of Nkarta. “He will be an enormous asset to the Nkarta board
and executive team as we execute our bold, strategic path to
pioneer safe and accessible cell therapy for people living with
lupus and other autoimmune diseases.”
Dr. Vratsanos graduated from New York University (NYU) School of
Medicine with honors and completed a postdoctoral fellowship in
investigative rheumatology/immunobiology at Yale University. He
also earned a master’s degree in clinical investigation from
Vanderbilt University, as well as a bachelor’s degree and master’s
degree in biomedical engineering from Columbia University.
“I’m excited to embrace this new leadership opportunity and
support Nkarta’s ground-breaking clinical work to explore natural
killer cell therapy for the treatment of lupus and other autoimmune
diseases,” Vratsanos said. “Nkarta’s mission is my own. My passion
is the translation of innovative immune science into approved
therapies that transform patient care. NK cell therapy has
breakthrough potential to treat debilitating autoimmune diseases
without the safety concerns and logistical challenges of other cell
therapies. I look forward to helping Nkarta leverage its strengths
as it advances its cell therapy programs.”
Nkarta is working to harness the body's natural killer (NK)
cells – the immune system's first responders – to deliver a safe,
well tolerated, accessible form of cell therapy to treat autoimmune
disease. NKX019, an allogeneic, on-demand cell therapy candidate,
is in development to treat lupus nephritis – a severe form of lupus
in which the immune system attacks the kidneys and other healthy
tissue and organs.
About NKX019NKX019 is an allogeneic,
cryopreserved, off-the-shelf immunotherapy candidate that uses
natural killer (NK) cells derived from the peripheral blood of
healthy adult donors. It is engineered with a humanized
CD19-directed CAR for enhanced cell targeting and a proprietary,
membrane-bound form of interleukin-15 (IL-15) for greater
persistence and activity without exogenous cytokine support. CD19
is a biomarker for normal B cells as well as those implicated in
autoimmune disease and B cell-derived malignancies.
About NkartaNkarta is a clinical-stage
biotechnology company advancing the development of allogeneic,
off-the-shelf natural killer (NK) cell therapies. By combining its
cell expansion and cryopreservation platform with proprietary cell
engineering technologies and CRISPR-based genome engineering
capabilities, Nkarta is building a pipeline of future cell
therapies engineered for deep therapeutic activity and intended for
broad access in the outpatient treatment setting. For more
information, please visit the company’s website at
www.nkartatx.com.
Cautionary Note on Forward-Looking
StatementsStatements contained in this press release
regarding matters that are not historical facts are
“forward-looking statements” within the meaning of the Private
Securities Litigation Reform Act of 1995, as amended. Words such as
"anticipates," "believes," "expects," "intends," “plans,”
“potential,” "projects,” “would” and "future" or similar
expressions are intended to identify forward-looking statements.
Examples of these forward-looking statements include, but are not
limited to, statements concerning Nkarta’s expectations regarding
any or all of the following: the value and benefits to Nkarta of
Dr. Vratsanos joining Nkarta’s Board; Nkarta’s position, plans, and
strategies for the continued and future clinical development and
commercial potential of its product candidates, including NKX019,
for the treatment of autoimmune disease; and the therapeutic
potential, accessibility, tolerability, advantages, and safety
profile of NK cell therapies, including NKX019 for the treatment of
autoimmune diseases, such as lupus.
Because such statements are subject to risks and uncertainties,
actual results may differ materially from those expressed or
implied by such forward-looking statements. These risks and
uncertainties include, among others: Nkarta’s limited operating
history and historical losses; Nkarta’s lack of any products
approved for sale and its ability to achieve profitability; the
risk that the results of preclinical studies and early-stage
clinical trials may not be predictive of future results; Nkarta’s
ability to raise additional funding to complete the development and
any commercialization of its product candidates; Nkarta’s
dependence on the clinical success of NKX019; that Nkarta may be
delayed in initiating, enrolling or completing its clinical trials;
competition from third parties that are developing products for
similar uses; Nkarta’s ability to obtain, maintain and protect its
intellectual property; Nkarta’s dependence on third parties in
connection with manufacturing, clinical trials and pre-clinical
studies; and the complexity of the manufacturing process for CAR NK
cell therapies.
These and other risks and uncertainties are described more fully
in Nkarta’s filings with the Securities and Exchange Commission
(“SEC”), including the “Risk Factors” section of Nkarta’s Quarterly
Report on Form 10-Q for the quarter ended March 31, 2024, filed
with the SEC on May 9, 2024, and Nkarta’s other documents
subsequently filed with or furnished to the SEC. All
forward-looking statements contained in this press release speak
only as of the date on which they were made. Except to the extent
required by law, Nkarta undertakes no obligation to update such
statements to reflect events that occur or circumstances that exist
after the date on which they were made.
Nkarta Media/Investor Contact:Greg MannNkarta,
Inc.gmann@nkartatx.com
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