First patient receives brain-responsive
neuromodulation for LGS, a severe and disabling childhood-onset
epilepsy
NeuroPace, Inc. (Nasdaq: NPCE), a commercial-stage medical
device company focused on transforming the lives of people living
with epilepsy, today announced that the first patient with
Lennox-Gastaut Syndrome (LGS) was treated in its feasibility
investigational device exemption (IDE) study. LGS is a devastating
form of childhood onset epilepsy characterized by cognitive
dysfunction and frequent generalized onset seizures that often lead
to injury. The study uses the RNS® System, which has demonstrated
safety and effectiveness of brain-responsive stimulation for
treating medically intractable focal onset seizures in people 18
and older, to test whether brain-responsive neurostimulation can
also be used to treat LGS.
The first procedure took place at Emory Healthcare in Atlanta
and was performed by Robert E. Gross, MD, PhD, the MBNA Bowman
Chair in Neurosurgery and Professor and Vice Chair, Emory
University Department of Neurosurgery. “An exciting aspect of this
study is that the implant location for each patient is based on
customized models of their brain connectivity.”
NeuroPace received a $9.3 million National Institutes of Health
(NIH) grant through the Brain Research through Advancing Innovative
Neurotechnologies® (BRAIN Initiative) to evaluate its responsive
neuromodulation technology in those who suffer from LGS. Six study
sites will enroll a total of 20 patients 12 years of age and older
with LGS and drug-resistant generalized onset seizures.
“The NIH looks for ideas that could be transformative, with the
potential to change how LGS is treated today,” said Martha Morrell,
MD, Chief Medical Officer of NeuroPace. “In addition to finding the
best detection and stimulation settings for responsive
neurostimulation in LGS, we are looking to identify changes in the
recorded brain data that indicate whether the therapy is effective.
These so-called biomarkers may help clinicians treat LGS and also
facilitate future research, including the possibility of a larger
clinical study into the mechanisms of the disease and treatment
approaches.”
Presently, antiseizure medications are the standard of care for
treatment of LGS. However, even with multiple medications, seizures
are rarely controlled, and it is typical for people with LGS to
experience increasing disability over their lifetime.
"Overall, treatment is rarely effective in LGS, and the outcome
remains very poor," said Tracy Dixon-Salazar, PhD, Executive
Director of the LGS Foundation and mother of an adult living with
LGS. "Those living with LGS need new treatment options for the many
seizures, LGS-associated disorders, and treatment side-effects our
loved ones suffer. The impact of LGS extends to the whole family,
as we shoulder this unpredictable disease and try to manage the
many physical, emotional, and financial burdens. We need better
treatments now."
Disclaimer: Research reported in this press release was
supported by the National Institutes of Health’s Brain Research
Through Advancing Innovative Neurotechnologies (BRAIN) Initiative
under award number UH3NS109557. The content is solely the
responsibility of the authors and does not necessarily represent
the official views of the National Institutes of Health.
About Epilepsy
One in 26 Americans will develop epilepsy in their lifetime,
with approximately 150,000 new cases of epilepsy diagnosed
annually. An estimated 3.4 million Americans currently live with
epilepsy. Epilepsy is a chronic disorder, the hallmark of which is
recurrent, unprovoked seizures. More people live with epilepsy than
autism spectrum disorder, Parkinson’s disease, multiple sclerosis
and cerebral palsy – combined.[i]
About the RNS® System
The RNS® System, a paradigm-shifting treatment for
drug-resistant focal epilepsy, is the only brain-responsive
neuromodulation system approved by the FDA. The closed-loop
technology delivers personalized, data-driven treatment targeted to
the seizure source by continuously monitoring brain activity,
recognizing a patient’s unique seizure pattern, and responding in
real-time with imperceptible stimulation to prevent seizures. By
recording ongoing EEG data, the RNS System provides physicians with
a unique “window to the brain,” enabling them to remotely monitor
their patients, gain insights based on brain activity, and use that
information to optimize patient care. Long-term clinical studies
demonstrate that the RNS System provides significant reduction in
seizure frequency and enduring improvements in quality of life and
cognition with no stimulation-related side effects. The RNS System
is available at most comprehensive epilepsy centers in the United
States and is widely covered by insurance. It is currently approved
in the United States as an adjunctive therapy for patients 18 years
of age and older with drug-resistant focal epilepsy. See important
safety information at www.neuropace.com/safety/.
About NeuroPace, Inc.
Based in Mountain View, Calif., NeuroPace is a commercial-stage
medical device company focused on transforming the lives of people
living with epilepsy by reducing or eliminating the occurrence of
debilitating seizures. Its novel and differentiated RNS System is
the first and only commercially available, brain-responsive
platform that delivers personalized, real-time treatment at the
seizure source. This platform can drive a better standard of care
for patients suffering from drug-resistant epilepsy and has the
potential to offer a more personalized solution and improved
outcomes to the large population of patients suffering from other
brain disorders.
Forward Looking Statements
In addition to background and historical information, this press
release contains “forward-looking statements” based on NeuroPace’s
current expectations, forecasts and beliefs, including NeuroPace’s
expectations and beliefs about future growth and indication
expansion, commercialization efforts, expected returns, growth
plans and revenue expectations, as well as our assumptions
underlying these expectations. These forward-looking statements are
subject to inherent uncertainties, risks, and assumptions that are
difficult to predict, including the possibility of delays or
failures associated with implementation, regulatory actions,
failure to maintain or renew key customer and other business
relationships, failure to maintain competitive offerings, the
possibility of unfavorable results, and other risks associated with
our commercialization efforts or business. You should not put undue
reliance on these statements or the information presented. These
and other risks and uncertainties include those described more
fully in the section titled “Risk Factors” and “Management’s
Discussion and Analysis of Financial Condition and Results of
Operation” and elsewhere in its public filings with the U.S.
Securities and Exchange Commission (SEC), including its Annual
Report on Form 10-K for the year ended December 31, 2021 filed with
the SEC on March 10, 2022 and its quarterly report on Form 10-Q
filed with the SEC on November 8, 2022, as well as any reports that
it may file with the SEC in the future. Forward-looking statements
contained in this announcement are based on information available
to NeuroPace as of the date hereof. NeuroPace undertakes no
obligation to update such information except as required under
applicable law. These forward-looking statements should not be
relied upon as representing NeuroPace’s views as of any date
subsequent to the date of this press release and should not be
relied upon as a prediction of future events. In light of the
foregoing, investors are urged not to rely on any forward-looking
statement in reaching any conclusion or making any investment
decision about any securities of NeuroPace.
[i]Epilepsy Foundation. “Facts about Seizures and
Epilepsy.”
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version on businesswire.com: https://www.businesswire.com/news/home/20221130005182/en/
Media Contacts: Health+Commerce for NeuroPace Shay Smith
shay@healthandcommerce.com
Investor Contact: Gilmartin Group Philip Trip Taylor
investors@neuropace.com
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