Mochida Pharmaceutical Company, Ltd.
18
0
0
17
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
Low Risk
Score: 25/100
0.0%
0 terminated/withdrawn out of 18 trials
100.0%
+13.5% vs industry average
56%
10 trials in Phase 3/4
18%
3 of 17 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (18)
Efficacy of Ethyl Icosapentate in Patients With Severe Hypertriglyceridemia
Role: lead
A Study of MD-120 in Patients With Depression
Role: lead
Drug-drug Interaction Study of FYU-981 and Oxaprozin
Role: lead
Long-term Safety and Efficacy Study of MND-2119 in Patients With Hypertriglyceridemia
Role: lead
A Study Comparing LBAL to Humira® in Subjects With Active Rheumatoid Arthritis Despite Methotrexate Therapy
Role: collaborator
Efficacy of MND-2119 in Participants With Hypertriglyceridemia
Role: lead
Study of FYU-981 in Hyperuricemia With or Without Gout
Role: collaborator
Benzbromarone-Controlled, Double-Blind, Comparative Study of FYU-981 in Hyperuricemia With or Without Gout
Role: collaborator
Study of FYU-981 in Hyperuricemic Outpatients With or Without Gout (Effect on Two Hyperuricemic Types)
Role: lead
Clinical Pharmacology of FYU-981 (Subjects With Hepatic Insufficiency)
Role: lead
Febuxostat-Controlled, Double-Blind, Comparative Study of FYU-981 in Hyperuricemia With or Without Gout
Role: lead
Utility of Presepsin in Distinguishing Between Sepsis and SIRS
Role: lead
Mass Balance Study of FYU-981
Role: collaborator
Clinical Pharmacology of FYU-981 (Final Formulation)
Role: lead
A Study Comparing LBEC0101 to Enbrel® in Subjects With Active Rheumatoid Arthritis Despite Methotrexate Therapy
Role: collaborator
Protective Effect of EPA on Cardiovascular Events
Role: collaborator
Double-Blind, Placebo-Controlled Study of Two Doses of EPA-E in Patients With Non Alcoholic Steatohepatitis (NASH)
Role: lead
Study Evaluating Single Ascending Doses of MR1817
Role: lead
All 18 trials loaded