Summary

Eligibility
for people ages 12 months to 24 months (full criteria)
Location
at San Francisco, California and other locations
Dates
study started
completion around
Principal Investigator
by Joseph Sullivan, MD
Headshot of Joseph Sullivan
Joseph Sullivan

Description

Summary

Dravet syndrome is a genetic epilepsy associated with pathogenic variants in SCN1A that codes for Nav1.1, a protein necessary for sodium channels. Children with Dravet syndrome classically present in the first year of life with prolonged seizures, often hemiclonic and in the setting of fever or temperature changes such as getting in or out of bath water. Many anti-seizure medications are sodium channel blockers and exacerbate seizures in this patient population. This creates some limitations in medication choices for this patient population. Recently fenfluramine was approved for use in Dravet syndrome for people 2 years and older. Randomized studies demonstrated a 74.9% reduction of convulsive motor seizures compared to 19.2% in the placebo group. Additionally, 16% of children treated with fenfluramine were seizure free. Fenfluramine is likely to be as effective in children under the age of 2 years. The current study has proposed a treatment protocol to allow access to fenfluramine for children under 24 months of age.

Official Title

Assessment of Safety of the Use of Fenfluramine in Children with Dravet Syndrome Under the Age of 24 Months

Keywords

Dravet Syndrome (DS), Children Under 2 Years, Fenfluramine, Dravet Syndrome, Myoclonic Epilepsies, Syndrome

Eligibility

You can join if…

Open to people ages 12 months to 24 months

Treating physicians must submit a clinical statement of potential benefit to the lead site for review of the multi-PIs, which includes patient's gender, age, diagnosis, genetic pathogenic variant, co-morbidities, seizure history, prior and current therapies, response to prior therapies and reason for request. Echocardiogram (ECHO) results must also be submitted to the lead site prior to final approval. Patients must be between 12 and 23 months old to be eligible. Each subject will be reviewed by the multi-PIs to ensure agreement that the subject has Dravet syndrome. Additional inclusion criteria:

  1. SCN1A with a known or presumed pathogenic variant or VUS with a history of prolonged seizure or a clinical diagnosis of Dravet syndrome.
  2. Failure of at least one anti-seizure medication that is not a sodium channel blocker (lamotrigine, oxcarbazepine, carbamazepine, eslicarbazepine)

You CAN'T join if...

  1. Patients with mild or greater mitral valve regurgitation and/or trace or greater aortic valve regurgitation will not be eligible for participation. The clinical statement can be submitted first for initial, conditional approval and then ECHO results can be submitted at a later date for final approval.
  2. Patients with failure to thrive will not be eligible for participation as fenfluramine can suppress appetite and has a risk for weight loss. Failure to thrive will be evaluated on the following criteria:
    1. Weight less than the 2nd percentile.
    2. Lack of weight gain that crosses two or more of the major percentile lines and is not congruent with length.

Inclusion of patients will be at the sole discretion of the multi-PIs based on a majority vote.

Locations

  • UCSF
    San Francisco California 94143 United States
  • Children's Hospital Colorado
    Aurora Colorado 80045 United States
  • Mayo Clinic
    Rochester Minnesota 55905 United States

Lead Scientist at UCSF

  • Joseph Sullivan, MD
    Professor, Neurology, School of Medicine. Authored (or co-authored) 55 research publications

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of Colorado, Denver
ID
NCT06598449
Phase
Phase 4 research study
Study Type
Interventional
Participants
Expecting 12 study participants
Last Updated