developmental and epileptic encephalopathy
Information
- Disease name
- developmental and epileptic encephalopathy
- Disease ID
- DOID:0112202
- Description
- "An electroclinical syndrome characterized by epileptiform activity and at least one other pathology that together contribute to cognitive and behavioral impairments including developmental delay or regression with onset anywhere from birth to adulthood." [url:https\://pubmed.ncbi.nlm.nih.gov/28276062/, url:https\://pubmed.ncbi.nlm.nih.gov/31926847/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT05626634 | Active, not recruiting | Phase 2 | Open-label, Long-term Safety Study of LP352 in Subjects With Developmental and Epileptic Encephalopathy | November 8, 2022 | October 2024 |
| NCT05364021 | Completed | Phase 1/Phase 2 | Study to Investigate LP352 in Subjects With Developmental and Epileptic Encephalopathies | March 3, 2022 | November 20, 2023 |
| NCT04937062 | Enrolling by invitation | Early Phase 1 | Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathy | March 1, 2021 | December 31, 2025 |
| NCT06380192 | Not yet recruiting | Developmental and Epileptic Encephalopathy of Genetic Etiology: Natural History Through Reuse of Clinical Data | May 1, 2024 | March 31, 2026 |
- Disase is a (Disease Ontology)
- DOID:0050701
- Cross Reference ID (Disease Ontology)
- MIM:PS308350