Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 100/100

Failure Rate

48.0%

12 terminated/withdrawn out of 25 trials

Success Rate

36.8%

-49.7% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

43%

3 of 7 completed trials have results

Key Signals

4 recruiting3 with results11 terminated

Enrollment Performance

Analytics

Phase 1
21(91.3%)
Phase 2
2(8.7%)
23Total
Phase 1(21)
Phase 2(2)

Activity Timeline

Global Presence

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Clinical Trials (25)

Showing 20 of 25 trials
NCT07570862Phase 2Not Yet Recruiting

A Phase 2, Open-Label, Single-Arm Trial of FT819 in Participants With Lupus Nephritis

Role: lead

NCT06308978Phase 1Recruiting

A Phase 1 Study of FT819 in B-cell Mediated Autoimmune Disease

Role: lead

NCT07560865Phase 1Recruiting

First-in Cancer-Type Phase I Study of FT536 for Recurrent WHO Grade 4 Astrocytoma

Role: collaborator

NCT04629729Phase 1Active Not Recruiting

FT819 in Subjects With B-cell Malignancies

Role: lead

NCT07216105Phase 1Recruiting

FT836 With or Without Chemotherapy and/or Monoclonal Antibodies, in Participants With Advanced Solid Tumors

Role: lead

NCT05182073Phase 1Completed

FT576 in Subjects With Multiple Myeloma

Role: lead

NCT06241456Phase 1Recruiting

FT825/ONO-8250, an Off-the-Shelf, HER2 CAR-T, With or Without Monoclonal Antibodies in Advanced Solid Tumors

Role: lead

NCT05950334Phase 1Completed

FT522 With Rituximab in Relapsed/Refractory B-Cell Lymphoma (FT522-101)

Role: lead

NCT04023071Phase 1Terminated

FT516 in Subjects With Advanced Hematologic Malignancies

Role: lead

NCT04245722Phase 1Terminated

FT596 as a Monotherapy and in Combination With Anti-CD20 Monoclonal Antibodies

Role: lead

NCT04551885Phase 1Terminated

FT516 in Combination With Monoclonal Antibodies in Advanced Solid Tumors

Role: lead

NCT05395052Phase 1Terminated

FT536 Monotherapy and in Combination With Monoclonal Antibodies in Advanced Solid Tumors

Role: lead

NCT04614636Phase 1Terminated

FT538 in Subjects With Advanced Hematologic Malignancies

Role: lead

NCT05069935Phase 1Terminated

FT538 in Combination With Monoclonal Antibodies in Advanced Solid Tumors

Role: lead

NCT04106167Terminated

Long-term, Non-interventional, Observational Study Following Treatment With Fate Therapeutics FT500 Cellular Immunotherapy

Role: lead

NCT05934097Phase 1Withdrawn

FT596 in Combination With R-CHOP in Subjects With B-Cell Lymphoma

Role: lead

NCT03841110Phase 1Completed

FT500 as Monotherapy and in Combination With Immune Checkpoint Inhibitors in Subjects With Advanced Solid Tumors

Role: lead

NCT02743351Phase 1Completed

Study of ProTmune for Allogeneic HCT in Adult Patients With Hematologic Malignancies

Role: lead

NCT04093622Terminated

Long-term Follow-Up Study Following Treatment With Fate Therapeutics' Engineered Cellular Immunotherapy

Role: lead

NCT01627314Phase 2Terminated

The PUMA Trial is a Trial of a Single ProHema Modulated-Cord Blood (CB) Unit as Part of a Double CB Transplant in Patients With Hematologic Malignancies.

Role: lead