2026 Hawaii Comprehensive Epilepsy Center & Epilepsy Research Unit Awarded Study to Investigate (JZP926 or Epidiolex) for the Treatment of Developmental and Epileptic Encephalopathy (DEE)

Honolulu, October 2026

Neurologists, epileptologists and researchers at Hawaii's Comprehensive Epilepsy Center and Epilepsy Research Unit

The neurologists, epileptologists and research team of Hawaii’s Comprehensive Epilepsy Center & Epilepsy Research Unit.

The Hawaii Comprehensive Epilepsy Center and Epilepsy Research Unit have been awarded a new Phase 3 study investigating JZP926 (CBD oral solution, Epidiolex) for the treatment of developmental and epileptic encephalopathy (DEE).

The study brings an advanced epilepsy treatment option to Hawaii, so that local families no longer have to travel to the mainland to take part in research of this kind.

What Is Developmental and Epileptic Encephalopathy?

Developmental and epileptic encephalopathy (DEE) refers to a group of severe epilepsies characterized by seizures that are often drug-resistant. The term encephalopathy describes significant developmental delay, or even the loss of developmental skills already gained.

In the DEEs, two separate factors contribute to developmental delay. This distinction matters for treatment: if seizure control can be improved, the epileptic encephalopathy component of the delay should also improve.

About Epidiolex

Epidiolex cannabidiol 100 mg/mL oral solution

Epidiolex is a prescription oral solution containing highly purified, plant-derived cannabidiol (CBD). It is FDA-approved to treat Lennox-Gastaut syndrome (LGS), Dravet syndrome, and tuberous sclerosis complex (TSC).

It works through several pathways at once. It binds to TRPV1 channels and GPR55 receptors to reduce calcium influx into brain cells, and interacts with ENT-1 to alter adenosine signaling. Together these actions dampen excess release of glutamate, the brain’s primary excitatory chemical, which helps stabilize abnormal electrical activity across neural networks.

About the Study

This is a Phase 3, multicenter, randomized, placebo-controlled, double-blind study evaluating the efficacy and safety of CBD oral solution (CBD-OS) in participants with DEE.

Phase 3

Randomized, double-blind, placebo-controlled

Age 1+

Participants aged 1 year and older with DEE

6 Weeks

Double-blind treatment period

The primary objective of the 6-week double-blind treatment period is to assess whether CBD-OS reduces the frequency of countable motor seizures compared with placebo in participants with DEE.

Darren Dugas, MD, Neurologist and Principal Investigator, Hawaii Pacific Neuroscience

“Our neurologists, epileptologists & researchers at Hawaii’s Comprehensive Epilepsy Center & Epilepsy Research Unit are honored to contribute to this important study and making available this option to our local island populations who no longer has to travel to Mainland for advanced epilepsy treatments.”

— Darren Dugas, MD, Neurologist & Principal Investigator, Comprehensive Epilepsy Center and Video-EEG Epilepsy Monitoring Unit (EMU), Hawaii Epilepsy Research Unit

Learn More or Enroll

To ask about taking part, contact our dedicated epilepsy research hotline:

📞 (808) 564-6141

✉️ info@HawaiiNeuroscience.com

View the Study on ClinicalTrials.gov

Study identifier: NCT07723976. Eligibility is determined by the study team after a screening evaluation.

 

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