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synucleinopathy - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

synucleinopathy

MONDO:0000510

Also known as:alpha synucleinopathiessynucleinopathies

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Overview

A neurodegenerative disease that is characterized by the abnormal accumulation of aggregates of alpha-synuclein protein in neurons, nerve fibers or glial cells. [url:http://en.wikipedia.org/wiki/Synucleinopathies ]

Clinical Trials16 registered · 9 recruiting

Diagnosis

Biomarker and diagnostic research for synucleinopathy has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

16 clinical trials registered, 9 recruiting. Interventions under study include other interventions and drug therapy. Pipeline includes 3 PHASE2, 1 EARLY_PHASE1, 4 NA. Research is sponsored by a mix of industry and academic institutions.

NCT ID	Title	Phase	Sponsor	Status
[NCT06193252](https://clinicaltrials.gov/study/NCT06193252)

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 1:52 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

→Are any of the 16 active clinical trials a good fit for my situation?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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Research Type	Count	% of Total
Laboratory research	121	40%
Research summaries	67	22%
Testing and diagnosis research	45	15%
Disease patterns and progression	41	14%
New treatment approaches	11	4%
Clinical study results	7	2%
Other research	4	1%
Patient case studies	3	1%

synucleinopathy

Overview

Diagnosis

Research Landscape

Medical References

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Questions for Your Care Team

Questions for Your Care Team

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