Success Metrics

Clinical Success Rate
60.0%

Based on 3 completed trials

Completion Rate
60%(3/5)
Active Trials
3(30%)
Results Posted
100%(3 trials)
Terminated
2(20%)

Phase Distribution

Ph phase_1
5
50%
Ph phase_2
1
10%
Ph phase_3
3
30%

Phase Distribution

5

Early Stage

1

Mid Stage

3

Late Stage

Phase Distribution9 total trials
Phase 1Safety & dosage
5(55.6%)
Phase 2Efficacy & side effects
1(11.1%)
Phase 3Large-scale testing
3(33.3%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

60.0%

3 of 5 finished

Non-Completion Rate

40.0%

2 ended early

Currently Active

3

trials recruiting

Total Trials

10

all time

Status Distribution
Active(5)
Completed(3)
Terminated(2)

Detailed Status

Completed3
Terminated2
Active, not recruiting2
Enrolling by invitation2
Recruiting1

Development Timeline

Analytics

Development Status

Total Trials
10
Active
3
Success Rate
60.0%
Most Advanced
Phase 3

Trials by Phase

Phase 15 (55.6%)
Phase 21 (11.1%)
Phase 33 (33.3%)

Trials by Status

completed330%
recruiting110%
terminated220%
active_not_recruiting220%
enrolling_by_invitation220%

Recent Activity

Clinical Trials (10)

Showing 10 of 10 trials
NCT06270719

An Observational Study Comparing Delandistrogene Moxeparvovec (ELEVIDYS) With Standard of Care in Participants With Duchenne Muscular Dystrophy

Enrolling By Invitation
NCT04626674Phase 1

A Gene Transfer Therapy Study to Evaluate the Safety of and Expression From Delandistrogene Moxeparvovec (SRP-9001) in Participants With Duchenne Muscular Dystrophy (DMD)

Recruiting
NCT06128564Phase 2

A Gene Delivery Study to Evaluate the Safety and Expression of Delandistrogene Moxeparvovec in Participants Under the Age of Four With Duchenne Muscular Dystrophy (DMD)

Active Not Recruiting
NCT05967351Phase 3

A Long-term Follow-up Study of Participants Who Received Delandistrogene Moxeparvovec (SRP-9001) in a Previous Clinical Study

Enrolling By Invitation
NCT06241950Phase 1

A Gene Transfer Therapy Study to Evaluate the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) Following Imlifidase Infusion in Participants With Duchenne Muscular Dystrophy (DMD) Determined to Have Pre-existing Antibodies to Recombinant Adeno-Associated Virus Serotype (rAAVrh74)

Terminated
NCT06597656Phase 1

A Gene Transfer Therapy to Evaluate the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) Following Therapeutic Plasma Exchange (Plasmapheresis) in Participants With Duchenne Muscular Dystrophy (DMD) and Pre-existing Antibodies to AAVrh74

Terminated
NCT05096221Phase 3

A Gene Transfer Therapy Study to Evaluate the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) in Participants With Duchenne Muscular Dystrophy (DMD)

Completed
NCT05881408Phase 3

A Gene Transfer Therapy Study to Evaluate the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) in Non-Ambulatory and Ambulatory Participants With Duchenne Muscular Dystrophy (DMD)

Active Not Recruiting
NCT03375164Phase 1

A Gene Transfer Therapy Study to Evaluate the Safety of Delandistrogene Moxeparvovec (SRP-9001) in Participants With Duchenne Muscular Dystrophy (DMD)

Completed
NCT03769116Phase 1

A Randomized, Double-blind, Placebo-controlled Study of Delandistrogene Moxeparvovec (SRP-9001) for Duchenne Muscular Dystrophy (DMD)

Completed

All 10 trials loaded

Drug Details

Intervention Type
GENETIC
Total Trials
10