Cellectis S.A.
6
2
3
0
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
High Risk
Score: 100/100
50.0%
3 terminated/withdrawn out of 6 trials
0.0%
-86.5% vs industry average
0%
0 trials in Phase 3/4
0%
0 of 0 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (6)
Phase 1/2 Study of UCART22 in Patients With Relapsed or Refractory CD22+ B-cell Acute Lymphoblastic Leukemia (BALLI-01)
Role: lead
Study Evaluating UCART20x22 in B-Cell Non-Hodgkin Lymphoma
Role: lead
Study Evaluating Safety and Efficacy of UCART123v1.2 in Patients With Relapsed/Refractory Acute Myeloid Leukemia
Role: lead
Study Evaluating Safety and Efficacy of UCART Targeting CS1 in Patients With Relapsed/Refractory Multiple Myeloma (MELANI-01)
Role: lead
Phase I Study of UCART123 in Patient With Adverse Genetic Risk Acute Myeloid Leukemia
Role: lead
Study to Evaluate the Safety and Clinical Activity of UCART123 in Patients With BPDCN
Role: lead
All 6 trials loaded