Could a seizure drug also prevent sudden death in dravet syndrome?
NCT ID NCT07112365
First seen Jun 27, 2026 · Last updated Jul 16, 2026 · Updated 2 times
Summary
This study tests whether the drug Fintepla (fenfluramine) can improve how the brain and lungs respond to carbon dioxide in people with Dravet syndrome, a severe epilepsy. Poor responses to CO2 may increase the risk of sudden unexpected death in epilepsy (SUDEP). Twenty-five participants will take Fintepla for about 60 days and undergo brain scans and breathing tests to measure changes.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- Fenfluramine (Fintepla)
- What this could lead to
- If it works, this could point toward a way to lower the risk of sudden unexpected death in epilepsy (SUDEP) for people with Dravet syndrome.
- What could go wrong
- This is a small, early-stage study with only 25 participants, so results may not apply to everyone. It focuses on brain and breathing changes, not directly on preventing death, so benefits are uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
The University of Texas Health Science Center at Houston
RECRUITINGHouston, Texas, 77030, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Virtual therapy helps kids with rare epilepsy gain daily living skills
- New hope for dravet syndrome: phase 3 trial of EPX-100 aims to cut seizures
- Could a repurposed drug tame seizures in adult dravet patients?
- New hope for rare epilepsy: fenfluramine made available for dravet patients
- New hope for kids with rare seizure disorder: ION337 trial launches