ALS
Pipeline by Development Stage
Drug Modality Breakdown
Competitive Landscape
14 companies ranked by most advanced pipeline stage
Trial Timeline
Clinical trial activity over time
Showing 15 of 18 trials with date data
Clinical Trials (20)
Total enrollment: 7,126 patients across 20 trials
Efficacy and Safety Extension Study of Oral Edaravone Administered in Subjects With ALS
Efficacy and Safety Study of Oral Edaravone Administered in Subjects With ALS
Safety Study of Oral Edaravone Administered in Subjects With ALS
Safety and Efficacy of Ranolazine for the Treatment of Amyotrophic Lateral Sclerosis
A Trial of Tocilizumab in ALS Subjects
Talampanel for Amyotrophic Lateral Sclerosis (ALS)
Multicenter Trial for Adults With Partial Seizures
Open-label Extension (OLE) Study of WVE-004 in Patients With C9orf72-associated Amyotrophic Lateral Sclerosis (ALS) and/or Frontotemporal Dementia (FTD)
Study of WVE-004 in Patients With C9orf72-associated Amyotrophic Lateral Sclerosis (ALS) or Frontotemporal Dementia (FTD)
A Pilot Trial of Triheptanoin for People With Amyotrophic Lateral Sclerosis (PALS)
Effects of Talampanel on Patients With Advanced Parkinson's Disease
A Study of TCD601 (Siplizumab) in Newly Diagnosed Adult Amyotrophic Lateral Sclerosis (ALS) Patients
A Phase 1 Study to Investigate the Safety and Pharmacokinetics of Fosigotifator in Patients With Amyotrophic Lateral Sclerosis
Multimodal Imaging Outcome Measures for ALS (Image ALS)
A Phase 1 Study to Investigate the Effects of Talampanel on the Heart Rhythm
Scalable Expanded Access With Analysis of Neurofilament and Other Biomarkers for Ibudilast in ALS
Intermediate Expanded Access Protocol CNMAu8.EAP04
Digital Tools for Assessment of Motor Functions and Falls in ALS
Genomic Translation for Amyotrophic Lateral Sclerosis Care
ALS/MND Natural History Study Data Repository
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.