Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 50/100

Failure Rate

12.9%

4 terminated/withdrawn out of 31 trials

Success Rate

85.2%

-1.3% vs industry average

Late-Stage Pipeline

13%

4 trials in Phase 3/4

Results Transparency

61%

14 of 23 completed trials have results

Key Signals

1 recruiting14 with results

Enrollment Performance

Analytics

Phase 1
14(48.3%)
Phase 2
11(37.9%)
Phase 3
3(10.3%)
Phase 4
1(3.4%)
29Total
Phase 1(14)
Phase 2(11)
Phase 3(3)
Phase 4(1)

Activity Timeline

Global Presence

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Clinical Trials (31)

Showing 20 of 31 trials
NCT07531251Phase 4Not Yet Recruiting

Clinical Trial in Patients With Barth Syndrome- 4TAZPower

Role: lead

NCT05168774Phase 1Completed

FRDA Investigator Initiated Study (IIS) With Elamipretide

Role: collaborator

NCT07275424Phase 2Recruiting

Study of Healthy Aging and Physical Function With Elamipretide

Role: collaborator

NCT06373731Phase 3Active Not Recruiting

ReNEW:Phase 3 Study of Efficacy, Safety & Pharmacokinetics of Subcutaneous Injections of Elamipretide in Subjects With Dry Age-Related Macular Degeneration (Dry AMD)

Role: lead

NCT05162768Phase 3Completed

Study to Evaluate Efficacy and Safety of Elamipretide in Subjects With Primary Mitochondrial Disease From Nuclear DNA Mutations (nPMD)

Role: lead

NCT04689360Unknown

An Intermediate Size Expanded Access Protocol of Elamipretide

Role: lead

NCT03891875Phase 2Completed

ReCLAIM-2 Study to Evaluate Safety,Efficacy & Pharmacokinetics of Elamipretide in Subjects With AMD With Non-central GA

Role: lead

NCT03098797Phase 2Completed

A Trial to Evaluate Safety, Tolerability and Efficacy of Elamipretide in Subjects With Barth Syndrome

Role: lead

NCT03323749Phase 3Terminated

A Trial to Evaluate Safety and Efficacy of Elamipretide Primary Mitochondrial Myopathy Followed by Open-Label Extension

Role: lead

NCT02976038Phase 2Terminated

Open-Label Extension Trial to Characterize the Long-term Safety and Tolerability of Elamipretide in Subjects With Genetically Confirmed Primary Mitochondrial Myopathy (PMM)

Role: lead

NCT02693119Phase 2Completed

A Study Investigating the Safety, Tolerability, and Efficacy of Elamipretide Topical Ophthalmic Solution for Treatment of Leber's Hereditary Optic Neuropathy

Role: lead

NCT02653391Phase 1Completed

A Study Investigating the Safety, Tolerability, and Efficacy of Elamipretide Topical Ophthalmic Solution for the Treatment of Fuchs' Corneal Endothelial Dystrophy (FCED)

Role: lead

NCT02848313Phase 1Completed

An Open-Label, Phase 1 Clinical Study to Evaluate the Safety and Tolerability of Subcutaneous Elamipretide in Subjects With Intermediate Age-Related Macular Degeneration

Role: lead

NCT01755858Phase 1Terminated

Effects of Intravenous Bendavia™ on Reperfusion Injury in Patients Undergoing Angioplasty of the Renal Artery

Role: lead

NCT02914665Phase 2Completed

A Phase 2 Study to Evaluate the Cardiac and Renal Effects of Short Term Treatment With Elamipretide in Patients Hospitalized With Congestion Due to Heart Failure

Role: lead

NCT02805790Phase 2Completed

Safety, Tolerability, Efficacy of MTP-131 for Treatment of Mitochondrial Disease in Subjects From the MMPOWER Study

Role: lead

NCT02245620Phase 2Completed

A Phase 2 Study to Evaluate the Impact of MTP-131 (Bendavia™) on Skeletal Muscle Function in Elderly

Role: lead

NCT01572909Phase 2Completed

Evaluation of Myocardial Effects of MTP-131 for Reducing Reperfusion Injury in Patients With Acute Coronary Events

Role: lead

NCT02788747Phase 2Completed

Effect of Elamipretide on Left Ventricular Function in Subjects With Stable Heart Failure With Reduced Ejection Fraction

Role: lead

NCT02367014Phase 1Completed

Safety, Tolerability, and Efficacy of MTP-131 for the Treatment of Mitochondrial Myopathy

Role: lead