Plain-English translation of NCT07010471 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Phase 3 — Testing in thousands of people, comparing the treatment against what doctors currently use. This is the last big step before approval.
This trial is testing a new medication called Relutrigine to help children and young people with developmental and epileptic encephalopathy (a severe form of epilepsy that affects development). The study will compare the medication to a placebo (a dummy pill with no active ingredient) to see if the medication is safe and can reduce seizures.
Severe childhood epilepsy can be very difficult to control with existing treatments, and children with this condition often continue to have seizures despite trying multiple medications. This trial is testing whether this new treatment option can help reduce seizures and improve safety in this group.
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You will be randomly assigned to receive either the new medication or a placebo once daily for 16 weeks. Neither you nor the research team will know which one you're receiving (this is called "double-blind"). After 16 weeks, if you choose, you can continue into an additional 32-week phase where everyone receives the active medication. Throughout the trial, you'll have clinic visits to check how you're doing and monitor for any side effects.
AI-generated summary from trial data · Jun 4, 2026 · Not medical advice
United States