Muscular Diseases
31
2
3
21
Key Insights
Highlights
Success Rate
88% trial completion (above average)
Clinical Risk Assessment
Based on trial outcomes
Low Risk
Score: 17/100
9.7%
3 terminated out of 31 trials
87.5%
+1.0% vs benchmark
26%
8 trials in Phase 3/4
43%
9 of 21 completed with results
Key Signals
Data Visualizations
Phase Distribution
Trial Status
Trial Success Rate
Benchmark: 86.5%
Based on 21 completed trials
Clinical Trials (31)
Non-invasive BCI-controlled Assistive Devices
Managed Access Program for Del-zota in Participants With DMD Mutations Amenable to Exon 44 Skipping
Long-Term Outcomes of Ataluren in Duchenne Muscular Dystrophy
A Phase 1 Study of Anitocabtagene Autoleucel for the Treatment of Subjects With Non-oncology Plasma Cell-related Diseases
A Study of Deramiocel (CAP-1002) in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
Extension of AOC 1001-CS1 (MARINA) Study in Adult Myotonic Dystrophy Type 1 (DM1) Patients
Mollii Suit and Fibromyalgia (EXOFIB 2)
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
Repeat of: A Study to Evaluate Efficacy and Safety of Sublingual TNX-102 SL Tablet Taken at Bedtime in Patients With Fibromyalgia
Fibromyalgia Integrative Training for Adolescents With Juvenile Fibromyalgia
A Study to Evaluate eFFIcacy and Safety of Sublingual TNX-102 SL Tablet Taken at Bedtime in Patients With fibRoMyalgia
Absorption, Metabolism, Excretion and Absolute Bioavailability of EDG-5506 in Healthy Volunteers
Virtual Path Planning for Image-guided Needle Interventions
Diagnoses Associated With Persistent Elevation of Creatine Kinase
Ultrasound Grayscale Analysis in ARDS covid19
Study of Pioglitazone in Sporadic Inclusion Body Myositis
New Imaging Biomarkers for Muscular Diseases - Multispectral Optoacoustic Imaging in Spinal Muscular Atrophy
An Extension Study of Ataluren (PTC124) in Participants With Nonsense Mutation Dystrophinopathy
Phase 3 Study of Ataluren in Participants With Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)
Non-invasive Molecular Imaging of Muscle Structure (MSOT_muscles)