spinocerebellar ataxia type 2
Information
- Disease name
- spinocerebellar ataxia type 2
- Disease ID
- DOID:0050955
- Description
- "An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene." [url:https\://ghr.nlm.nih.gov/condition/spinocerebellar-ataxia-type-2]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT05826171 | Active, not recruiting | N/A | Priming Motor Learning Through Exercise in People With Spinocerebellar Ataxia | February 6, 2023 | May 31, 2025 |
| NCT03408080 | Active, not recruiting | Phase 3 | Open Pilot Trial of BHV-4157 | December 15, 2017 | December 15, 2024 |
| NCT03701399 | Active, not recruiting | Phase 3 | Troriluzole in Adult Subjects With Spinocerebellar Ataxia | March 8, 2019 | October 2025 |
| NCT04268147 | Active, not recruiting | Instrumented Data Exchange for Ataxia Study | June 1, 2019 | June 30, 2024 | |
| NCT03120013 | Completed | N/A | Rehabilitative Trial With Cerebello-Spinal tDCS in Neurodegenerative Ataxia | February 6, 2017 | December 1, 2018 |
| NCT04288128 | Completed | Integrated Functional Evaluation of the Cerebellum | May 28, 2020 | June 1, 2022 | |
| NCT04153110 | Completed | N/A | Cerebello-Spinal tDCS as Rehabilitative Intervention in Neurodegenerative Ataxia | December 1, 2018 | January 1, 2021 |
| NCT01470729 | Completed | Biomarkers in Autosomal Dominant Cerebellar Ataxia | November 2011 | December 2015 | |
| NCT03347344 | Completed | Phase 3 | Clinical Trial With Riluzole in Spinocerebellar Ataxia Type 2 (ATRIL) | January 17, 2018 | December 14, 2020 |
| NCT03378414 | Not yet recruiting | Phase 2 | Umbilical Cord Mesenchymal Stem Cells Therapy (19#iSCLife®-SA) for Patients With Spinocerebellar Ataxia | December 31, 2024 | December 31, 2025 |
| NCT01060371 | Recruiting | Natural History Study of and Genetic Modifiers in Spinocerebellar Ataxias | April 2010 | May 19, 2024 | |
| NCT01793168 | Recruiting | Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford | July 2010 | December 2100 | |
| NCT04301284 | Withdrawn | Phase 2 | Study of CAD-1883 for Spinocerebellar Ataxia | June 2021 | December 2022 |
- Disase is a (Disease Ontology)
- DOID:1441
- Cross Reference ID (Disease Ontology)
- MIM:183090
- OrphaNumber from OrphaNet (Orphanet)
- 98756