Crick
HomeTrialsGenesDrugs23andMeGraphBlogContact
  • Home
  • Trials
  • Genes
  • Drugs
  • 23andMe
  • Graph
  • Blog
  • Contact
Crick

An open-source clinical intelligence platform. Explore clinical trials, gene networks, and molecular structures using public data sources.

Data Sources

  • ClinicalTrials.gov
  • OpenTargets
  • ClinVar
  • PubChem

Links

  • Contact
  • About
  • Privacy

© 2026 Crick. All rights reserved.

Crick is for educational purposes only. Not medical advice.

Results for “STXBP1 Encephalopathy with Epilepsy”

9 trials

Filters

Phase
Early Phase 1
Phase 1
Phase 2
Phase 3
Phase 4
Status
Recruiting
Active, Not Recruiting
Not Yet Recruiting
Completed
Enrolling by Invitation

Showing 9 of 9 results

Very early researchActive Not RecruitingNCT04937062
What this trial is testing

Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathy

Who this might be right for
STXBP1 Encephalopathy With Epilepsy, SLC6A1 Neurodevelopmental DisorderDevelopmental and Epileptic Encephalopathy
Weill Medical College of Cornell University 50
Not applicableLooking for participantsNCT06625112
What this trial is testing

A Multicentric European Study to Promote Clinical Trial Readiness for STXBP1-related Disorders

Who this might be right for
STXBP1 Encephalopathy With Epilepsy
European STXBP1 Consortium 120
Post-approval studies (Phase 4)Looking for participantsNCT05232630
What this trial is testing

Fenfluramine for the Treatment of Different Types of Developmental and Epileptic Encephalopathies: a Pilot Trial Exploring Epileptic and Non-epileptic Outcomes

Who this might be right for
Refractory EpilepsySYNGAP1 EncephalopathySTXBP1 Encephalopathy With Epilepsy+3 more
Hospital Ruber Internacional 20
Not applicableWithdrawnNCT05462054
What this trial is testing

Natural History Study in Pediatric Patients with STXBP1 Encephalopathy with Epilepsy

Who this might be right for
STXBP1 Encephalopathy with Epilepsy
Capsida Biotherapeutics, Inc.
Not applicableLooking for participantsNCT06555965
What this trial is testing

STXBP1 and SYNGAP1 Related Disorders Natural History Study

Who this might be right for
Genetic DiseaseSTXBP1 Encephalopathy With EpilepsySYNGAP1-Related Intellectual Disability
Children's Hospital of Philadelphia 600
Not applicableNot Yet RecruitingNCT06356233
What this trial is testing

Phenotyping and Identification of Biological Markers in STXBP1 Encephalopathy

Who this might be right for
STXBP1 Encephalopathy With Epilepsy
Fundación Iniciativa para las Neurociencias (FINCE) 10
Not applicableLooking for participantsNCT01238250
What this trial is testing

Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight

Who this might be right for
16P11.2 Deletion Syndrome16p11.2 Duplications1Q21.1 Deletion+181 more
Simons Searchlight 100,000
Testing effectiveness (Phase 2)Temporarily pausedNCT06983158
What this trial is testing

A Clinical Trial of CAP-002 Gene Therapy in Pediatric Patients With Syntaxin-Binding Protein 1 (STXBP1) Encephalopathy

Who this might be right for
Developmental and Epileptic Encephalopathy
Capsida Biotherapeutics, Inc. 12
Not applicableActive Not RecruitingNCT05161494
What this trial is testing

Gait in Rare Diseases

Who this might be right for
Tuberous SclerosisSTXBP1 Encephalopathy With Epilepsy
Universiteit Antwerpen 70