Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 35/100

Failure Rate

0.0%

0 terminated/withdrawn out of 18 trials

Success Rate

100.0%

+13.5% vs industry average

Late-Stage Pipeline

22%

4 trials in Phase 3/4

Results Transparency

15%

2 of 13 completed trials have results

Key Signals

2 recruiting2 with results

Enrollment Performance

Analytics

Phase 1
10(58.8%)
Phase 3
4(23.5%)
Phase 2
3(17.6%)
17Total
Phase 1(10)
Phase 3(4)
Phase 2(3)

Activity Timeline

Global Presence

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Clinical Trials (18)

Showing 18 of 18 trials
NCT07335601Phase 2Recruiting

Study to Evaluate Resmetirom in Post-Liver Transplant Patients With MASH

Role: lead

NCT07541469Recruiting

Rezdiffra Pregnancy and Lactation Registry

Role: lead

NCT02912260Phase 2Completed

Phase 2 Study of MGL-3196 in Patients With Non-Alcoholic Steatohepatitis (NASH)

Role: lead

NCT03038022Phase 2Completed

Study of MGL-3196 in Patients With Heterozygous Familial Hypercholesterolemia (HeFH)

Role: lead

NCT06397872Phase 1Completed

A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Multiple Oral Doses (6 Days) of 100 mg Resmetirom in Subjects With Severe Renal Impairment and in Matched Healthy Control Subjects With Normal Renal Function

Role: lead

NCT04951219Phase 3Active Not Recruiting

A Phase 3 Study to Evaluate Safety and Biomarkers of Resmetirom (MGL-3196) in Patients With Non-alcoholic Fatty Liver Disease (NAFLD), MAESTRO-NAFLD-Open-Label-Extension (MAESTRO-NAFLD-OLE)

Role: lead

NCT05500222Phase 3Active Not Recruiting

A Phase 3 Study to Evaluate the Effect of Resmetirom on Clinical Outcomes in Patients With Well-compensated NASH Cirrhosis (MAESTRO-NASH-OUTCOMES)

Role: lead

NCT03900429Phase 3Active Not Recruiting

A Phase 3 Study to Evaluate the Efficacy and Safety of MGL-3196 (Resmetirom) in Patients With NASH and Fibrosis

Role: lead

NCT04643795Phase 1Completed

Phase 1 Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Multiple Oral Doses of MGL-3196 in Subjects With Varying Degrees of Hepatic Impairment and Healthy Matched Control Subjects

Role: lead

NCT04197479Phase 3Completed

A Phase 3 Study to Evaluate Safety and Biomarkers of Resmetirom (MGL-3196) in Non Alcoholic Fatty Liver Disease Patients

Role: lead

NCT01367873Phase 1Completed

Ascending Single-Dose Study to Evaluate VIA-3196 in Healthy Subjects

Role: lead

NCT02542969Phase 1Completed

Drug Interaction Study of MGL-3196 With Rosuvastatin and Simvastatin

Role: lead

NCT04671069Phase 1Completed

Drug Interaction Study of MGL-3196 With Clopidogrel

Role: lead

NCT04671056Phase 1Completed

Drug Interaction Study of MGL-3196 With Pioglitazone

Role: lead

NCT03413124Phase 1Completed

Bioavailability Study of MGL-3196 Tablets Compared to Capsules

Role: lead

NCT03220165Phase 1Completed

Radiolabeled Study to Determine the Mass Balance of [14C] MGL-3196

Role: lead

NCT02749578Phase 1Completed

Drug Interaction Study of MGL-3196 With Atorvastatin

Role: lead

NCT01519531Phase 1Completed

Ascending Multiple-Dose Study to Evaluate VIA-3196 in Healthy Subjects

Role: lead

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