STXBP1 ENCEPHALOPATHY WITH EPILEPSY
Clinical trials for STXBP1 ENCEPHALOPATHY WITH EPILEPSY explained in plain language.
Never miss a new study
Get alerted when new STXBP1 ENCEPHALOPATHY WITH EPILEPSY trials appear
Sign up with your email to follow new studies for STXBP1 ENCEPHALOPATHY WITH EPILEPSY, keep track of the ones that matter, and come back to a personal dashboard instead of checking manually.
By submitting, you agree to our Terms of use
-
Scientists map rare brain disorder to pave way for First-Ever cures
Knowledge-focused Recruiting nowThis study aims to prepare for future clinical trials for STXBP1-related disorders, a rare and severe genetic condition causing seizures and developmental delays. Researchers will follow 120 patients over time to better understand how the disease progresses and to identify the be…
Matched conditions: STXBP1 ENCEPHALOPATHY WITH EPILEPSY
Sponsor: European STXBP1 Consortium • Aim: Knowledge-focused
Last updated Mar 30, 2026 14:30 UTC
-
Groundwork laid for future treatments of rare brain disorders
Knowledge-focused Recruiting nowThis study aims to learn more about two rare genetic brain disorders, STXBP1 and SYNGAP1, which cause severe developmental delays and epilepsy. Researchers will follow 600 participants for up to five years, tracking their symptoms and quality of life through regular check-ups and…
Matched conditions: STXBP1 ENCEPHALOPATHY WITH EPILEPSY
Sponsor: Children's Hospital of Philadelphia • Aim: Knowledge-focused
Last updated Mar 23, 2026 15:17 UTC