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Innovation

Shining a light on the treatment of CNS disorders and cancer care.

SK Life Science is here listening to the needs of healthcare providers, patients, caregivers, advocates, and scientists. We are developing new molecules, enhancing advocacy efforts, and providing solutions that change what’s possible in the treatment of CNS disorders and cancer care.

Our Medicines

SK Life Science is committed to accelerating the development of next generation treatments for CNS disorders and cancer care. SK Biopharmaceuticals and SK Life Science independently developed XCOPRI® (cenobamate tablets) CV from inception through FDA approval.

For More Information

The two companies also discovered and licensed-out the FDA and EMA-approved treatment for sleep disorders after completing phase 1 clinical trials.

U.S. Patent Rights For Products

This website is provided to satisfy the virtual patent marking provisions of the United States, including relevant provisions of the America Invents Act and 35 U.S. Code 287 (a).

The following products are protected by the associated U.S. patents set forth in the table below. The list is subject to change due to issuance of additional patents, product changes and other circumstances. The absence of a U.S. Patent number from the list does not constitute a waiver of the patent, trademark, or other intellectual property rights pertaining to the product.

  • XCOPRI®
    (cenobamate tablets) CV
    U.S. Patent No. 7,598,279
    U.S. Patent No. 11,654,133

For Healthcare Providers

Changing What’s Possible

For the latest scientific and clinical information about our medicines, please visit our medical information website. This resource provides up-to-date access to company-sponsored publications and recent medical conference presentations, helping you support your patients in leading healthier and happier lives.

For medical information inquiries on our medicines or to report adverse effects, please email us at Medicalinfo@SKLSI.com or call 1-866-OKSKLSI (657-5574).

Global Patient Safety

Ensuring the safety of patients is our top priority.

We do this through pharmacovigilance monitoring. For more information, please see here.

Our Clinical Trials

We are committed to conducting diverse, global clinical trials. With a commitment to safety, we place our patients at the center of everything we do.

To address the needs of the patient communities we serve, we are conducting the following clinical trials:

  • Global Primary Generalized Tonic-Clonic (PGTC) Seizures Clinical Trial
    Our global Phase 3 Open Label Safety Study for patients 12 years of age and older had sites in the U.S. as well as Bulgaria, Czechia, Georgia, Hungary, Poland, Slovakia, and Ukraine.
  • Global Pediatric Clinical Trial
    We are currently enrolling in a Phase 3 Open Label Safety Study for patients between the ages of 2 and 3. The trial is currently recruiting in the U.S. as well as in Australia, Germany, Hungary, Poland, South Korea, and Spain.
  • Global LGS DISCOVER Study
    The LGS DISCOVER study is evaluating whether an investigational drug can decrease the number of seizures in patients 4-55 years of age living with Lennox-Gastaut syndrome. The trial is currently recruiting in Australia, Colombia, Germany, Greece, Hungary, Italy, Korea, Mexico, Poland, Portugal, Serbia, Spain, Taiwan, and the U.S. For more information, please visit www.LGSDiscoverStudy.com.
  • Monotherapy Study
    This is an open-label study to evaluate the effectiveness, safety and tolerability of an investigational drug used as a monotherapy in newly diagnosed or recurrent partial-onset seizures adult patients between the ages of 18 and 74.
  • Global Phase 1 Radiopharmaceutical Therapy Clinical Trial
    This first-in-human, open-label, multicenter Phase 1 study is evaluating the safety, dose range, and biologically active dose of an investigational alpha-emitter radiopharmaceutical therapy (SKL35501) in patients with advanced solid tumors expressing NTSR1. The study is being conducted in the United States and South Korea and includes dose escalation followed by dose optimization and expansion.

Our Global Pipeline

SK Life Science and its parent company SK Biopharmaceuticals have 12 compounds under development globally.

Compound Indication
Discovery
Pre-Clinical
Phase 1
Phase 2
Phase 3
NDA
Marketed
Cenoba­mate
Epilepsy – Focal Seizures
Epilepsy – Focal Seizures, Asia 1
Epilepsy – Generalized Seizures2
Epilepsy – Focal Seizures, Pediatric
Solriamfetol (L/O to Axsome, Ignis)
EDS3 in Narcolepsy, EDS in OSA4
Carisbamate
Lennox-Gastaut Syndrome
SKL32276
Parkinson’s Diseases
(GCase Activator)
SKL24741
Epilepsy
SKL13865
ADHD
SKL20540
Schizophrenia
SKL35501 (FL-091)
Oncology
(targeting NTSR1)
SKL37321 (WT-7695)
Oncology
(targeting CA9)
ROR1 Project
Oncology
(targeting ROR1)
p300 Degrader
Oncology
(targeting p300)
Neuroimmune Project
CNS
(targeting VAV1)

1) NDA approved in Korea, China(Nov. 2025, Dec. 2025 for each), Submitted NDA in Japan(Sep. 2025)
2) Primary Generalized Tonic-Clonic(PGTC) seizures, Phase 3 topline data obtained in Sep. 2025
3) Excessive Daytime Sleepiness
4) Obstructive Sleep Apnea

Invigorating Next Generation Discovery

We are a group of scientists, inventors, and explorers tirelessly working to develop solutions that will improve CNS and cancer care

Leveraging Technologies to Include:

  • Target-based drug discovery techniques
  • High throughput organic screening (HTOs)/high content screening (HCS)
  • Computer-aided drug design (CADD)
  • Combinatorial chemistry

Key R&D Sectors:

We deploy our technologies in the areas of biology/discovery, medicinal chemistry, and pharmacology. The goal of research in these areas is to bring meaningful products to market.

Select A Sector For Details

We are responsible for lead compound discovery and optimization. This sector:

  • IDENTIFIES and validates signal and molecular targets
  • DEVELOPS screening technologies
  • PERFORMS high-throughput screening (HTS) leveraging technologies
  • PARTICIPATES in joint studies on targets known to have high target-disease correlation
  • INVESTIGATES the efficacy and safety of lead compounds

The medicinal chemistry sector of SK Life Science is responsible for:

  • IDENTIFYING a wide array of drug candidates for the treatment of CNS disorders and cancer
  • OPTIMIZING lead compounds in terms of their structure-activity relationships
  • DEVELOPING processes for clinical candidates to lead compound discovery and optimization

To maximize efficiency, we have implemented a CADD system, a high-efficiency synthesis infrastructure, an established structure-diverse library, and a target focus library.

The pharmacology sector is responsible for research programs in which drug candidates are studied to enable prediction of drug activity in the human body.

Grant Requests

Medical Education Grant Request

  • Please complete and submit the form below, along with the following documents to request an Investigator Initiated Studies (IIS). The Review Committee will review the request and determine if there is interest in the proposal.  An email will be sent after the review is complete and a decision is made.  Study requestor will be notified within 30 days of submission.

    Accepted file types: pdf, docx, doc, txt, png, jpg, jpeg, ppt, pptx, xlsx, xls, csv, Max. file size: 20 MB.
    Accepted file types: pdf, docx, doc, txt, png, jpg, jpeg, ppt, pptx, xlsx, xls, csv, Max. file size: 20 MB.
    This form must be completed with the study institution information that will be receiving payment.
    Accepted file types: pdf, docx, doc, txt, png, jpg, jpeg, ppt, pptx, xlsx, xls, csv, Max. file size: 20 MB.

    Contact Information

    Study Information

    Please provide the expected benefits and new challenges that may emerge based on the outcome of this proposal. Challenges could be a result of inferences and or misperceptions based on study outcome(s). Regional differences could exist and if so, provide context. If not applicable, enter “NA”.

    To healthcare providers

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    To XCOPRI’s Lifecycle

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