New hope for babies with severe epilepsy: early access to fenfluramine

NCT ID NCT06598449

First seen May 17, 2026 · Last updated May 28, 2026 · Updated 5 times

Summary

This study is for children aged 12 to 23 months with Dravet syndrome, a severe genetic epilepsy that causes long seizures often triggered by fever. The drug fenfluramine is already approved for children 2 years and older and has been shown to greatly reduce seizures. This expanded access program aims to give younger children the same treatment while carefully monitoring safety. Only 5 children will take part, and doctors must provide a statement of potential benefit before enrollment.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Children's Hospital Colorado

    RECRUITING

    Aurora, Colorado, 80045, United States

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••

Conditions

Explore the condition pages connected to this study.