RecruitingPhase 3NCT07221292
Neurological
Spinocerebellar ataxia type 2
4
studies recruiting now
as of 7 Sept 2026
26
studies registered in total
as of 7 Sept 2026
10
countries with a recruiting site
as of 7 Sept 2026
27 Oct 2025
most recent study posted
among recruiting studies
Recruiting trials
RecruitingNCT01060371
Natural History Study of and Genetic Modifiers in Spinocerebellar Ataxias
RecruitingNot applicableNCT07136844
Gait Analysis Parameter and Upper Limb Evaluation in Adult Patients With Neurological or Metabolic Pathology
RecruitingNCT01793168
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
Showing the 4 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.
Search all Spinocerebellar ataxia type 2 studiesWhere recruiting studies are running
Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.
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Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Spinocerebellar ataxia type 2
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the gene involved (ATXN2).
Treatments being studied
2 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.
Phase 3Riluzole (Exservan)
Phase 2Lithium Carbonate (Camcolit 250)
Related conditions
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).