SK Biopharmaceuticals is recognized in the digital health category for two wearable devices – Zero Glasses TM and Zero Wired TM– becoming the first Korean pharma to earn this accolade
Pangyo, Gyeonggi Province, Korea, Nov. 16, 2022 – SK Biopharmaceuticals, an innovative global pharmaceutical company, announced that it has been named a CES® 2023 Innovation Awards Honoree for outstanding design and engineering of two wearable devices – Zero GlassesTM
and Zero WiredTM.
SK Biopharmaceuticals will become the first Korean pharmaceutical company to earn such an accolade in the category of digital health. The announcement came ahead of the CES 2023, the world’s most influential and biggest technology event that will be held January 5-8 in Las Vegas, Nevada.
Zero Glasses, smart glasses, and Zero Wired, a wired device
connectable to mobile phones, are integrated wearable devices that can
detect and forecast seizure by measuring bio-signals from brain
activity, heart rhythm, and body movement.
They are compatible with SK Biopharmaceuticals’ mobile application named Zero AppTM
that can record and analyze bio-signal data in real time. The wearable
devices can be worn comfortably in both professional and private
The names of the wearable devices derive from SK Biopharmaceuticals’
key mission to strive for the potential of “zero seizures” for patients
through cenobamate, an anti-seizure medication (ASM) approved by the
U.S. Food and Drug Administration for the treatment of partial-onset
(focal-onset) seizures in adults. It is commercially available in the
U.S. under the brand name XCOPRI® (cenobamate tablets) CV. SK
Biopharmaceuticals operates in the U.S. through SK Life Science, a
subsidiary based in New Jersey.
SK Biopharmaceuticals will showcase the wearable devices and provide
an on-site demonstration at CES 2023. The CES Innovation Awards program,
owned and produced by the Consumer Technology Association (CTA)®, is an
annual competition honoring outstanding design and engineering in 28
consumer technology product categories.
About SK Biopharmaceuticals
SK Biopharmaceuticals and its U.S. subsidiary SK Life Science are
global pharmaceutical companies focused on the research, development and
commercialization of treatments for disorders of the central nervous
system (CNS). The companies have a pipeline of eight compounds in
development for the treatment of CNS disorders, including epilepsy.
Additionally, SK Biopharmaceuticals is focused on early research in
oncology. For more information, visit SK Biopharmaceuticals’ website at www.skbp.com/eng and SK Life Science’s website at www.SKLifeScienceInc.com.
Cenobamate is an anti-seizure medication (ASM) discovered and
developed by SK Biopharmaceuticals and SK life science. While
the precise mechanism by which cenobamate exerts its therapeutic effect
is unknown, it is believed to reduce repetitive neuronal firing by
inhibiting voltage-gated sodium currents. It is also a
positive allosteric modulator of the γ-aminobutyric acid (GABAA) ion channel.
Cenobamate is approved in the United States for the treatment
of partial-onset seizures in adults and is available under the brand
name XCOPRI® (cenobamate tablets) CV. Cenobamate can be combined with
other ASMs or used alone. The recommended initial dosage
of cenobamate is 12.5 mg once-daily, with titration every two weeks; it
is available in six tablet strengths for once-daily dosing: 12.5 mg, 25
mg, 50 mg, 100 mg, 150 mg and 200 mg.
Cenobamate is also approved in the European Union and the United
Kingdom for the adjunctive treatment of focal-onset (partial-onset)
seizures with or without secondary generalization in adult patients with
seizures that have not been adequately controlled despite a history of
treatment with at least two anti-epileptic medicinal products and is
marketed by Angelini Pharma under the brand name ONTOZRY®.
Additionally, cenobamate is in clinical development in Asia. Ono
Pharmaceutical and Ignis Therapeutics have the rights to develop and
commercialize cenobamate in Japan and in the Greater China region,
respectively. SK Biopharmaceuticals has recently entered into an
exclusive licensing agreement with Endo for cenobamate in Canada.
IMPORTANT SAFETY INFORMATION AND INDICATION FOR XCOPRI® (cenobamate tablets) CV
DO NOT TAKE XCOPRI IF YOU:
Are allergic to cenobamate or any of the other ingredients in XCOPRI.
Have a genetic problem (called Familial Short QT syndrome) that affects the electrical system of the heart.
XCOPRI CAN CAUSE SERIOUS SIDE EFFECTS, INCLUDING:
Allergic reactions: XCOPRI can cause serious skin rash or
other serious allergic reactions which may affect organs and other parts
of your body like the liver or blood cells. You may or may not
have a rash with these types of reactions. Call your healthcare
provider right away and go to the nearest emergency room if you have any
of the following: swelling of your face, eyes, lips, or tongue, trouble
swallowing or breathing, a skin rash, hives, fever, swollen glands, or
sore throat that does not go away or comes and goes, painful sores in
the mouth or around your eyes, yellowing of your skin or eyes, unusual
bruising or bleeding, severe fatigue or weakness, severe muscle pain,
frequent infections, or infections that do not go away. Take
XCOPRI exactly as your healthcare provider tells you to take it. It is
very important to increase your dose of XCOPRI slowly, as instructed by
your healthcare provider.
QT shortening: XCOPRI may cause problems with the electrical system of the heart (QT shortening). Call
your healthcare provider if you have symptoms of QT shortening
including fast heartbeat (heart palpitations) that last a long time or
Suicidal behavior and ideation: Antiepileptic drugs,
including XCOPRI, may cause suicidal thoughts or actions in a very
small number of people, about 1 in 500. Call your health care provider
right away if you have any of the following symptoms, especially if they
are new, worse, or worry you: thoughts about suicide or dying;
attempting to commit suicide; new or worse depression, anxiety, or
irritability; feeling agitated or restless; panic attacks; trouble
sleeping (insomnia); acting aggressive; being angry or violent; acting
on dangerous impulses; an extreme increase in activity and talking
(mania); or other unusual changes in behavior or mood.
Nervous system problems: XCOPRI may cause problems
that affect your nervous system. Symptoms of nervous system problems
include: dizziness, trouble walking or with coordination, feeling sleepy
and tired, trouble concentrating, remembering, and thinking clearly,
and vision problems. Do not drive, operate heavy machinery, or do other dangerous activities until you know how XCOPRI affects you.
Do not drink alcohol or take other medicines that can make
you sleepy or dizzy while taking XCOPRI without first talking to your
Do not stop taking XCOPRI without first talking to your healthcare provider. Stopping
XCOPRI suddenly can cause serious problems. Stopping seizure medicine
suddenly in a patient who has epilepsy can cause seizures that will not
stop (status epilepticus).
XCOPRI may affect the way other medicines work, and other medicines may affect how XCOPRI works. Do not start or stop other medicines without talking to your healthcare provider. Tell
healthcare providers about all the medicines you take, including
prescription and over-the-counter medicines, vitamins and herbal
PREGNANCY AND LACTATION:
XCOPRI may cause your birth control medicine to be less effective. Talk to your health care provider about the best birth control method to use.
Talk to your health care provider if you are pregnant or plan to become pregnant. It
is not known if XCOPRI will harm your unborn baby. Tell your healthcare
provider right away if you become pregnant while taking XCOPRI. You and
your healthcare provider will decide if you should take XCOPRI while
you are pregnant. If you become pregnant while taking XCOPRI, talk to
your healthcare provider about registering with the North American
Antiepileptic Drug (NAAED) Pregnancy Registry. The purpose of this
registry is to collect information about the safety of antiepileptic
medicine during pregnancy. You can enroll in this registry by calling
1-888-233-2334 or go to www.aedpregnancyregistry.org.
Talk to your health care provider if you are breastfeeding or plan to breastfeed. It
is not known if XCOPRI passes into breastmilk. Talk to your healthcare
provider about the best way to feed your baby while taking XCOPRI.
COMMON SIDE EFFECTS:
The most common side effects in patients taking XCOPRI include
dizziness, sleepiness, headache, double vision, and feeling tired.
These are not all the possible side effects of XCOPRI. Tell your
healthcare provider if you have any side effect that bothers you or that
does not go away. For more information, ask your healthcare provider or
pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www.fda.gov/medwatch.
XCOPRI is a federally controlled substance (CV) because it can be abused or lead to dependence. Keep XCOPRI in a safe place to prevent misuse and abuse. Selling or giving away XCOPRI may harm others and is against the law.
INDICATION: XCOPRI is a prescription medicine
used to treat partial-onset seizures in adults 18 years of age and
older. It is not known if XCOPRI is safe and effective in children under
18 years of age.
Please see additional patient information in the Medication Guide. This information does not take the place of talking with your healthcare provider about your condition or your treatment.