Clin2
NCT06504511Possibly a fitRecruiting

SCN1A gene study for epilepsy patients in the UK

SCN1ADravet SyndromeEpilepsy

Part of Brain & nervous system clinical trials.

This study aims to better understand SCN1A-related epilepsies by following patients over time. Researchers hope to learn more about how the condition progresses to help develop future treatments.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
400 people
Ages
Any age
Study type
Observational

Who can take part

  • You must be willing to sign a consent form agreeing to take part.
  • You must be able to attend virtual visits from home.
  • You must have a genetic test showing a specific SCN1A gene change.
  • You must not have any other serious illness that could interfere with the study.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT07251673Recruiting
Study of Dravet syndrome in children with SCN1A gene changes

This study follows children with Dravet syndrome caused by a specific SCN1A gene change to understand how the condition develops over time. It may help families know more about what to expect.

Paris, Ap-hp / DRCI
NCT05651204Recruiting
Study of brain GABA signals in Dravet syndrome

This study looks at “GABA signals” in the body/brain to learn more about Dravet syndrome and how it may relate to seizures. If you have Dravet syndrome caused by a specific SCN1A gene change, you may be asked to provide genetic test results and help with study visits so researchers can compare biomarker readings.

Fort Worth, Texas
NCT05419492Recruiting· Phase 1/Phase 2
ETX101 for children with SCN1A Dravet syndrome

This early-phase study tests how safe ETX101 is and whether it can help reduce seizures in young children with Dravet syndrome caused by an SCN1A gene change. It mainly enrolls infants and children with a specific type of seizure history and genetic result.

San Francisco, California
NCT07531745Recruiting· Phase 1/Phase 2
ION337 gene therapy for children with Dravet syndrome

This study tests a new gene therapy called ION337 designed to treat Dravet syndrome, a severe childhood epilepsy caused by a SCN1A gene mutation. The therapy is given as a spinal fluid injection and aims to reduce seizures in children ages 2–12.

Ann Arbor, Michigan
NCT06585605Recruiting
Study of epilepsy and movement disorder genes in children

This study looks at children with epilepsy and movement disorders to better understand the genes involved. It aims to help doctors recognize and treat these conditions more effectively.

Boston, Massachusetts
NCT05126914Recruiting
Follow-up study for rare epilepsy in children

This study follows children and teens with rare forms of epilepsy to better understand their condition over time in real-life care. It may help doctors improve future care plans and support for families.

Angers

Hear when a new Dravet Syndrome trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.