Nkarta Presents NKX101 Clinical Data at the 2023 American Society of Hematology Annual Meeting & Exposition
December 09 2023 - 8:31PM
Nkarta, Inc. (Nasdaq: NKTX), a clinical-stage biopharmaceutical
company developing engineered natural killer (NK) cell therapies,
today announced a poster presentation at the 2023 American Society
of Hematology (ASH) Annual Meeting and Exposition featuring
follow-up data from its Phase 1 clinical trial that evaluates
NKX101 in patients with relapsed or refractory acute myeloid
leukemia (r/r AML). NKX101 is an allogeneic, off-the-shelf NK cell
therapy candidate derived from healthy donors and engineered to
target NKG2D ligands.
As reported in June 2023, of those patients who received NKX101
after a disease-specific lymphodepletion (LD) regimen comprising
fludarabine and cytarabine (Flu/Ara-C), four of six achieved
CR/CRi. In the follow up presented today, three of those four
patients remained in CR/CRi at 4 months from treatment with NKX101.
No cases of cytokine release syndrome (CRS), immune effector
cell-associated neurotoxicity syndrome (ICANS), or
graft-versus-host disease (GvHD) of any grade were observed in
these patients.
“While this data set is small, we’re encouraged to see responses
and early durability in patients with high-risk features, including
those who have relapsed after stem cell transplantation. Recent
progress in therapy for r/r AML has been limited to targeted
therapies, which only help a minority of patients. This all-comers
study seeks to help patients without targetable mutations as well
as those for whom these treatments are ineffective,” noted David R.
Shook, MD, Chief Medical Officer of Nkarta. “We continue to
evaluate NKX101 following Flu/Ara-C in this high-need patient
population.”
Nkarta plans to provide an update from the NKX101 Flu/Ara-C LD
cohort in the first half of 2024 that includes preliminary safety
and response data from 12 to 20 additional patients.
Nkarta’s 2023 ASH poster will be available for download shortly
after its scheduled presentation at
http://www.nkartatx.com/publications/.
About NKX101NKX101 is an allogeneic,
cryopreserved, off-the-shelf cancer immunotherapy candidate that
uses natural killer (NK) cells derived from the peripheral blood of
healthy donors. It is engineered with a chimeric antigen receptor
(CAR) targeting NKG2D ligands on tumor cells. NKG2D, a key
activating receptor found on naturally occurring NK cells, induces
a cell-killing immune response through the detection of stress
ligands that are widely expressed on cancer cells. NKX101 is also
engineered with a membrane-bound form of interleukin-15 (IL15) for
greater persistence and activity without exogenous cytokine
support.
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 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, but are not limited to, statements concerning
Nkarta’s expectations regarding any or all of the following:
Nkarta’s position, plans, strategies, and timelines for the
continued and future clinical development and commercial potential
of NK cell therapies, including NKX101; the therapeutic potential,
accessibility, tolerability and safety profile of NK cell
therapies, including NKX101 for the treatment of AML; and Nkarta’s
plans and timelines for the future availability and disclosure of
NKX101 clinical trial data. Interim clinical data for NKX101
included in this press release 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 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 its two
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 our business of the COVID-19 pandemic or
similar public health crises.
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
September 30, 2023, filed with the SEC on November 9, 2023, 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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