The CurePSP Genetics Program
The CurePSP Genetics Program
Recruiting · NCT06647641 · Registry updated 2026-01-14Clinical trials
Swipe the table sideways for more columns.
| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| The CurePSP Genetics Program | Multiple system atrophy (MSA) with orthostatic hypotension, Neurologic Manifestations, Ocular Motility Disorders, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, autonomic nervous system disorder, basal ganglia disorder, brain disorder, cardiovascular disorder, central nervous system disorder, corticobasal degeneration disorder, cranial nerve neuropathy, eye disorder, hypotensive disorder, movement disorder, multiple system atrophy, multiple system atrophy, cerebellar type, multiple system atrophy, parkinsonian type, nervous system disorder, neurodegenerative disease, ophthalmoplegia, palsy, primary dysautonomia, progressive supranuclear palsy, supranuclear palsy, progressive, 1, synucleinopathy, tauopathy, vascular disorder | Recruiting | Not stated | 2026-01-14 | NCT06647641 |
3 results · Page 1 of 1
Organizations
Swipe the table sideways for more columns.
| Organizations | Linked trials |
|---|---|
| CurePSP Foundation | 2 |
| Massachusetts General Hospital | 758 |
| National Institutes of Health (NIH) | 667 |
1 results · Page 1 of 1
Research sites
Swipe the table sideways for more columns.
| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Massachusetts General Hospital | Boston | United States | 1015 |