Nkarta Promotes David R. Shook, M.D., to Chief Medical Officer
January 09 2023 - 4:30PM
Nkarta, Inc. (Nasdaq: NKTX), a clinical-stage biopharmaceutical
company developing engineered natural killer (NK) cell therapies to
treat cancer, today announced the promotion of David R. Shook,
M.D., to the role of Chief Medical Officer. Dr. Shook has extensive
expertise in cell therapy development and continues to lead
Nkarta’s global clinical development and regulatory operations.
“Dave has been a driving force behind the
development and execution of Nkarta’s clinical strategy using
off-the-shelf NK cell therapeutics since he joined our
organization,” said Paul J. Hastings, President and CEO of Nkarta.
“His expertise in the biology and engineering of NK cells, clinical
development experience, and proven leadership will strengthen our
mission to bring life-changing cell therapies to patients.”
An early pioneer of NK cell therapy, Dr. Shook
joined Nkarta in 2020 and was appointed as Vice President, Clinical
Development in 2022. Prior to joining Nkarta, he designed and led
multiple first-in-human cell therapy clinical trials, including the
use of CD19 CAR-NK cells, and he remains a practicing pediatric
oncologist and transplant physician. He was a fellow, fellowship
director and faculty member at St. Jude Children’s Research
Hospital, where he conducted research in the laboratory of Dario
Campana, M.D., Ph.D., Nkarta’s scientific founder. Dr. Campana and
Dr. Shook co-developed the membrane bound form of interleukin-15
(IL-15), a key component of Nkarta’s engineered NK cell platform
technology. He received an M.D. from The Johns Hopkins University
School of Medicine and a B.S. from Purdue University.
“Our advanced technology platform and highly
scalable manufacturing process have culminated in ongoing clinical
programs advancing two first-in-class cell therapy candidates, each
with early compelling data. Nkarta is well positioned to lead the
next generation of cell therapies and make a meaningful impact on
underserved therapeutic areas, harnessing the potential safety and
dosing advantages of NK cells," said Dr. Shook. “I’m excited to
continue working with our talented clinical team, investigators,
and my fellow leaders at Nkarta to realize the profound potential
of our programs to transform patient care.”
About Nkarta Nkarta is a
clinical-stage biotechnology company advancing the development of
allogeneic, off-the-shelf natural killer (NK) cell therapies for
patients with cancer. 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 anti-tumor 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
Statements Statements 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 statements
concerning Nkarta’s expectations regarding any or all of the
following: the potential impact of executive appointments made by
Nkarta; Nkarta’s ability to advance its cell therapy candidates in
the clinic and deliver them to patients; and the potential impact
of Nkarta’s cell therapy candidates on patients. Interim clinical
data referenced in this press release were reported on April 25,
2022 (for NKX101) and December 5, 2022 (for NKX019) are subject to
the risk that one or more of the clinical outcomes may materially
change as patient enrollment continues and more data on existing
patients become available.
Because forward looking 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 success of its co-lead
product candidates, NKX101 and NKX019; that Nkarta may be delayed
in initiating, enrolling or completing any 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; the complexity of the manufacturing process for CAR NK
cell therapies; the availability of components and supplies
necessary for the conduct of our clinical trials; and risks
relating to the impact on Nkarta’s business of the COVID-19
pandemic or similar public health crises.
These and other risks 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 September 30, 2022, filed
with the SEC on November 9, 2022, 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 Mann Nkarta, Inc. gmann@nkartatx.com
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