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
-
Can mapping rare genetic variants unlock better care for autism-related disorders?
Knowledge-focused Recruiting nowThis international online study collects medical, behavioral, and developmental information from people with rare genetic changes that are linked to autism and other neurodevelopmental disorders. By partnering with families, researchers aim to build a detailed database to improve…
Matched conditions: STXBP1 ENCEPHALOPATHY WITH EPILEPSY
Sponsor: Simons Searchlight • Aim: Knowledge-focused
Last updated Jul 25, 2026 00:00 UTC
-
Groundbreaking study paves way for STXBP1 therapies
Knowledge-focused Recruiting nowThis study follows 120 people with STXBP1-related disorders, a rare genetic condition causing severe developmental delays and seizures. Researchers aim to track how the disease changes over time and identify the best ways to measure improvement. This work will help design future …
Matched conditions: STXBP1 ENCEPHALOPATHY WITH EPILEPSY
Sponsor: European STXBP1 Consortium • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:02 UTC
-
Researchers track rare genetic disorders to prepare for future treatments
Knowledge-focused Recruiting nowThis study is observing 600 people of any age with STXBP1 or SYNGAP1 gene mutations to better understand how these disorders affect development, seizures, and quality of life. No treatment is given; instead, researchers will collect data from routine clinical assessments over tim…
Matched conditions: STXBP1 ENCEPHALOPATHY WITH EPILEPSY
Sponsor: Children's Hospital of Philadelphia • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:55 UTC