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Amyotrophic Lateral Sclerosis (ALS)

Fatal motor neuron disease. ~10% familial, 90% sporadic. Genetic targets SOD1, C9orf72, FUS, and TDP-43 account for most familial cases. First gene-silencing therapy (tofersen) approved 2023.

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987
Papers (5yr)
12
Active trials
5
Tracked biomarkers
5
Related diseases
Research signals

Research activity in ALS gene-silencing mechanisms has increased substantially since tofersen's 2023 approval. Neuroinflammation and microglial activation appear in 23% of active ALS trials — up from 8% five years ago. View full research signals →

Tracked biomarkers
Neurofilament Light Chain (NfL)Strong evidence

Universal neuronal damage marker. Elevated in CSF and blood. Used as a secondary endpoint in 8 active ALS trials.

IL-6 / TNF-αModerate evidence

Neuroinflammatory cytokines. Elevated in ALS CSF. Cross-disease panel opportunity with MS biomarker work.

TDP-43 (CSF/plasma)Moderate evidence

Aggregation marker specific to ALS and FTD. Emerging assay technology improving detection sensitivity.

SOD1 (CSF)Emerging

Target engagement marker for SOD1-ASO therapies including tofersen. Used to confirm mechanism of action.

Active clinical trials
NCT IDDrugPhaseStatusSponsor
NCT04235492Tofersen (SOD1-ASO)Phase IIIRecruitingBiogen
NCT02588677MasitinibPhase IIIRecruitingAB Science
NCT04120740TDP-43 chaperonePhase IIActiveAcademic consortium

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Related diseases — shared mechanisms

Phase 1 primary cohort + monitored diseases

Research and educational use only. Information does not constitute medical advice, diagnosis, or treatment recommendations. Verify with primary literature. AI disclaimer →