Fate Therapeutics
Fate Therapeutics sponsors 22 registered US clinical trials on ClinicalTrials.gov, 3 of them currently recruiting, and 7 completed. 0 of these trials are in Phase 3-4 (later-stage) and 20 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Precursor B-Cell Acute Lymphoblastic Leukemia, with 1 trials.
Trial Pipeline
22 total, page 1 of 1
FT836 With or Without Chemotherapy and/or Monoclonal Antibodies, in Participants With Advanced Solid Tumors
NCT07216105
A Phase 1 Study of FT819 in B-cell Mediated Autoimmune Disease
NCT06308978
FT825/ONO-8250, an Off-the-Shelf, HER2 CAR-T, With or Without Monoclonal Antibodies in Advanced Solid Tumors
NCT06241456
FT819 in Subjects With B-cell Malignancies
NCT04629729
FT522 With Rituximab in Relapsed/Refractory B-Cell Lymphoma (FT522-101)
NCT05950334
FT536 Monotherapy and in Combination With Monoclonal Antibodies in Advanced Solid Tumors
NCT05395052
FT576 in Subjects With Multiple Myeloma
NCT05182073
FT538 in Combination With Monoclonal Antibodies in Advanced Solid Tumors
NCT05069935
FT538 in Subjects With Advanced Hematologic Malignancies
NCT04614636
FT516 in Combination With Monoclonal Antibodies in Advanced Solid Tumors
NCT04551885
FT596 as a Monotherapy and in Combination With Anti-CD20 Monoclonal Antibodies
NCT04245722
FT516 in Subjects With Advanced Hematologic Malignancies
NCT04023071
Long-term Follow-Up Study Following Treatment With Fate Therapeutics' Engineered Cellular Immunotherapy
NCT04093622
Long-term, Non-interventional, Observational Study Following Treatment With Fate Therapeutics FT500 Cellular Immunotherapy
NCT04106167
FT500 as Monotherapy and in Combination With Immune Checkpoint Inhibitors in Subjects With Advanced Solid Tumors
NCT03841110
FATE-NK100 as Monotherapy and in Combination With Monoclonal Antibody in Subjects With Advanced Solid Tumors
NCT03319459
Study of ProTmune for Allogeneic HCT in Adult Patients With Hematologic Malignancies
NCT02743351
A Trial of a Single ProHema-CB Product Transplant in Pediatric Patients With Inherited Metabolic Disorders
NCT02354443
A Phase 1 Trial of a Single ProHema® CB Product for Pediatric Patients With Hematologic Malignancies
NCT02354417
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.
NCT01627314
Single Treatment With FT1050 of an Ex-vivo Modulated Umbilical Cord Blood Unit
NCT01527838
Safety and Efficacy of ProHema Modulated Umbilical Cord Blood Units in Subjects With Hematologic Malignancies.
NCT00890500
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 19 |
| Phase 2 | 1 |
Therapeutic Areas
What the Pipeline for Fate Therapeutics Shows
According to the ClinicalTrials.gov registry, Fate Therapeutics is linked to 22 US clinical trials across every stage of research activity. Of those, 3 studies are currently recruiting, about 14% of the sponsor's indexed portfolio, and 7 are already marked complete, representing roughly 32% of the total.
The phase mix for Fate Therapeutics reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 20 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Fate Therapeutics is Precursor B-Cell Acute Lymphoblastic Leukemia with 1 linked trial, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.