Daiichi Pharmaceuticals
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1 terminated/withdrawn out of 8 trials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
13%
1 trials in Phase 3/4
0%
0 of 7 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (8)
Soblidotin and Gemcitabine in Treating Patients With Locally Advanced or Metastatic Solid Tumors
Role: lead
DX-8951f in Treating Previously Untreated Patients With Stage IIIB or Stage IV Non-small Cell Lung Cancer
Role: lead
Efficacy and Safety in Patients With Acute Coronary Syndrome Without ST-Segment Elevation
Role: collaborator
Study to Evaluate Efficacy of Shunt Operation for Idiopathic Normal Pressure Hydrocephalus
Role: collaborator
A Phase I Trial of Tecogalan Sodium (DS-4152) Administered as an Infusion Every 21 Days
Role: lead
A Phase I Trial of Tecogalan Sodium ( DS-4152 ) Administered as an Infusion Twice Weekly for 21 Days.
Role: lead
A Study of Tecogalan Sodium
Role: lead
A Phase I Trial of Tecogalan Sodium ( DS-4152 ) Administered as an Infusion Weekly x 4
Role: lead
All 8 trials loaded