Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

progressive muscular atrophy (PMA) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

progressive muscular atrophy

MONDO:0018687

Also known as:PMAprogressive spinal muscular atrophypure progressive muscular atrophy

Find Clinical TrialsTrials

Overview

A rare, milder form of amyotrophic lateral sclerosis. It is characterized by a slowly progressive clinical course. Signs and symptoms include muscle weakness, atrophy, and fasciculation.

Clinical Trials57 registered · 22 recruiting

Diagnosis

Biomarker and diagnostic research for progressive muscular atrophy 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.

57 clinical trials registered, 22 recruiting. Interventions under study include other interventions, drug therapy, medical devices, and procedural interventions. Pipeline includes 3 PHASE4, 4 PHASE3, 2 PHASE2. Research is sponsored by a mix of industry and academic institutions.

NCT ID	Title	Phase	Sponsor	Status
[NCT07047144](https://clinicaltrials.gov/study/NCT07047144)

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 6:21 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:454706

GARD

Genetic and Rare Diseases Info Center

GARD:21891

Questions for Your Care Team

→Are any of the 57 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?

← Back to All Diseases

Research Type	Count	% of Total
Research summaries	61	32%
Disease patterns and progression	44	23%
Laboratory research	28	15%
New treatment approaches	21	11%
Testing and diagnosis research	16	8%
Patient case studies	11	6%
Clinical study results	8	4%

progressive muscular atrophy

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications