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

Study acronym: ESCO
StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Notable Lead sponsor: Amsterdam UMC, location VUmc to European STXBP1 Consortium
    • Collaborators: 8 to 9
    v7
  2. Notable Trial status: Not Yet Recruiting to Recruitingv6 Show 4 more changesShow less
    • Study sites: 0 to 1
    • Primary completion date: Oct 1, 2029 to Oct 31, 2029
    • Study completion date: Oct 1, 2034 to Oct 31, 2034
    • Start date changed from estimate of Oct 1, 2025 to Nov 4, 2025
  3. Notable Primary completion date: Apr 1, 2029 to Oct 1, 2029
    • Start date: Apr 1, 2025 to Oct 1, 2025
    • Study completion date: Apr 1, 2034 to Oct 1, 2034
    v5
  4. Notable Lead sponsor: Kelsey Ax to Amsterdam UMC, location VUmcv4 Show 4 more changesShow less
    • Start date: Dec 1, 2024 to Apr 1, 2025
    • Primary completion date: Dec 1, 2029 to Apr 1, 2029
    • Study completion date: Dec 1, 2034 to Apr 1, 2034
    • Collaborators revised (8)
  5. Notable Start date: Nov 1, 2024 to Dec 1, 2024v3
  6. Minor Collaborators revised (8)v2
  7. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
STXBP1-related disorders (STXBP1-RD) are rare genetic neurodevelopmental disorders, caused by pathogenic variants in the gene STXBP1. The core clinical features of the disorder are developmental delay often leading to (severe) intellectual disability and seizures in most patients, although the phenotypic spectrum is variable. Behavioral problems and movement disorders are frequent comorbidities. STXBP1-RD are severe disorders with significant impact on the quality of life of the patients and their caregivers. At the moment, there is no cure for STXBP1-RD and treatment is largely limited to symptom control. Recent advances in the field of precision medicine and gene therapy have led to the identification of potential novel disease modifying therapies for STXBP1-RD that hold promise to reach clinical trials in the coming years. However, accurate and successful evaluation of such novel precision therapies in STXBP1-RD patients is challenging, given the rarity of the condition and the variable clinical spectrum. Furthermore, relevant clinical endpoints, taking into account the patients' and caregivers' perspective have not been identified to date. In this European collaborative study, the investigators will prospectively follow patients with STXBP1-RD during different phases of life (infantile period, childhood and adolescence/adulthood). The study aims to better understand the natural history and the phenotypic spectrum of the disease including the identification of disease modifiers. It further aims to identify relevant clinical endpoints (what to treat?) and robust outcome measures and biomarkers (how to measure?) for future clinical trials. The study is performed in close collaboration with different STXBP1 patient-caregiver communities across Europe.
Trial Details
NCT Number NCT06625112
Lead Sponsor European STXBP1 Consortium
Collaborators: Filadelfia Epilepsy Hospital, University Hospital Heidelberg, University Hospital, Antwerp, Istituto Giannina Gaslini, Genoa, Italy, Hospital Sant Joan de Deu, Amsterdam UMC, location VUmc, Sheba Medical Center, Aix Marseille Université, Hospital Ruber Internacional
Conditions
(from sponsor)
STXBP1 Encephalopathy With Epilepsy
Related terms Epilepsy, Epileptic Encephalopathy, Early Infantile, 4
Enrollment 120 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov