Key Insights

Highlights

Success Rate

96% trial completion (above average)

Published Results

11 trials with published results (39%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

3.6%

1 terminated out of 28 trials

Success Rate

95.7%

+9.1% vs benchmark

Late-Stage Pipeline

32%

9 trials in Phase 3/4

Results Transparency

50%

11 of 22 completed with results

Key Signals

11 with results96% success

Data Visualizations

Phase Distribution

24Total
Not Applicable (4)
P 1 (3)
P 2 (8)
P 3 (9)

Trial Status

Completed22
Recruiting3
Terminated1
Unknown1
Not Yet Recruiting1

Trial Success Rate

95.7%

Benchmark: 86.5%

Based on 22 completed trials

Clinical Trials (28)

Showing 20 of 20 trials
NCT07444333Not ApplicableNot Yet RecruitingPrimary

Cardiac Output and Fatigue in Friedreich's Ataxia

NCT02069509CompletedPrimary

Patient Registry of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS)

NCT02497534RecruitingPrimary

Biomarkers in Friedreich's Ataxia

NCT02316314RecruitingPrimary

Characterization of the Cardiac Phenotype of Friedreich's Ataxia (FRDA)

NCT07095062Not ApplicableRecruitingPrimary

Electroencephalogram in Patients With Friedreich's Ataxia for the Study of the Structural and Functional Connectome.

NCT02593773Phase 3CompletedPrimary

Safety, Tolerability and Efficacy of ACTIMMUNE® Dose Escalation in Friedreich's Ataxia Study

NCT02415127Phase 3CompletedPrimary

Safety, Tolerability and Efficacy of ACTIMMUNE® Dose Escalation in Friedreich's Ataxia

NCT02797080Phase 3CompletedPrimary

Long-Term Safety Extension Study of ACTIMMUNE® (Interferon γ-1b) in Children and Young Adults With Friedreich's Ataxia

NCT00697073Phase 3CompletedPrimary

Study to Assess the Safety and Tolerability of Idebenone in the Treatment of Friedreich's Ataxia Patients

NCT00537680Phase 3CompletedPrimary

Study to Assess the Efficacy, Safety and Tolerability of Idebenone in the Treatment of Friedreich's Ataxia

NCT04102501Phase 3CompletedPrimary

A Study to Assess Efficacy, Long Term Safety and Tolerability of RT001 in Subjects With Friedreich's Ataxia

NCT02179333Completed

Preliminary Study of the Scale To Assess Ataxia and Neurologic Dysfunction (STAND)

NCT01898884Phase 1CompletedPrimary

Safety and Pharmacology Study of VP 20629 in Adults With Friedreich's Ataxia

NCT02445794Phase 1CompletedPrimary

A First in Human Study of RT001 in Patients With Friedreich's Ataxia

NCT01728064Phase 2CompletedPrimary

Safety and Efficacy of EPI-743 in Patients With Friedreich's Ataxia

NCT02660112Phase 2CompletedPrimary

(+) Epicatechin to Treat Friedreich's Ataxia

NCT02840669Not ApplicableCompletedPrimary

A Study to Characterize the Cardiac Phenotype of Individuals With Friedreich's Ataxia (CARFA Study)

NCT01016366Phase 2CompletedPrimary

Safety Study of Carbamylated Erythropoietin to Treat Patients With the Neurodegenerative Disorder Friedreich's Ataxia

NCT01962363Phase 2CompletedPrimary

EPI-743 in Friedreich's Ataxia Point Mutations

NCT00905268Phase 3CompletedPrimary

A Study of Efficacy, Safety and Tolerability of Idebenone in the Treatment of Friedreich's Ataxia (FRDA) Patients

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