Key Insights

Highlights

Success Rate

86% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 39/100

Termination Rate

7.7%

1 terminated out of 13 trials

Success Rate

85.7%

-0.8% vs benchmark

Late-Stage Pipeline

15%

2 trials in Phase 3/4

Results Transparency

50%

3 of 6 completed with results

Key Signals

3 with results86% success

Data Visualizations

Phase Distribution

6Total
Not Applicable (1)
P 1 (2)
P 2 (1)
P 3 (2)

Trial Status

Completed6
Recruiting3
Active Not Recruiting2
Terminated1
Not Yet Recruiting1

Trial Success Rate

85.7%

Benchmark: 86.6%

Based on 6 completed trials

Clinical Trials (13)

Showing 13 of 13 trials
NCT07711730Not ApplicableRecruitingPrimary

Telecare Psychosocial and Cognitive Intervention for Children and Adolescents With Limb-Girdle Muscular Dystrophy

NCT06246513Phase 3Active Not RecruitingPrimary

A Trial to Learn More About an Experimental Gene Therapy Called Bidridistrogene Xeboparvovec (SRP-9003) as a Possible Treatment for Limb Girdle Muscular Dystrophy 2E/R4

NCT04475926Active Not RecruitingPrimary

A Study of the Natural History of Participants With LGMD2E/R4, LGMD2D/R3, LGMD2C/R5, and LGMD2A/R1 ≥ 4 Years of Age, Who Are Managed in Routine Clinical Practice

NCT06399770Not Yet RecruitingPrimary

The Role of Muscle Ultrasound in Assessment of Sample of Patients With Limb-girdle Muscular Dystrophy

NCT04054375Phase 2CompletedPrimary

Weekly Steroids in Muscular Dystrophy

NCT00390104Recruiting

Molecular Analysis of Patients With Neuromuscular Disease

NCT03783923Phase 3TerminatedPrimary

A Study of Deflazacort (Emflaza®) in Participants With Limb-Girdle Muscular Dystrophy 2I (LGMD2I)

NCT01403402Recruiting

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

NCT00457912CompletedPrimary

Genetic Characterization of Individuals With Limb Girdle Muscular Dystrophy

NCT02759302CompletedPrimary

MRI on Persons With Mutations in POMT2 Gene (LGMD2N)

NCT02635321CompletedPrimary

MRI and Muscle Involvement in Patients With Mutations in GMPPB

NCT00873782Phase 1Completed

Safety Study of Transvenous Limb Perfusion in Human Muscular Dystrophy

NCT00104078Phase 1Completed

Study Evaluating MYO-029 in Adult Muscular Dystrophy

Showing all 13 trials

Research Network

Activity Timeline