Taisho Pharmaceutical R&D Inc.
8
0
0
7
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
Moderate Risk
Score: 45/100
12.5%
1 terminated/withdrawn out of 8 trials
87.5%
+1.0% vs industry average
0%
0 trials in Phase 3/4
29%
2 of 7 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (8)
A Single Ascending and Repeated Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TS-142 in Healthy Participants
Role: lead
A Study to Evaluate the Safety and Efficacy of TS-121 as an Adjunctive Treatment for Major Depressive Disorder
Role: lead
First-in-Human Study With Single and Multiple Doses of TS-161 in Healthy Participants
Role: lead
Safety, Tolerability and Pharmacokinetics of Single Doses of TS-134 in Healthy Volunteers
Role: lead
Safety, Tolerability and Pharmacokinetics of 14-day Multiple Dose Titrations of TS-134 in Healthy Volunteers
Role: lead
Effects of TS-134 on Ketamine-induced BOLD Signals in Healthy Subjects
Role: lead
Exploratory Study Using Positron Emission Tomography With TS-121 and [11C]TASP0410699 in Healthy Adult Male Subjects
Role: lead
Study of TS-022 in Adult Patients With Atopic Dermatitis With Pruritus (POC)
Role: lead
All 8 trials loaded