> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/company/fate-therapeutics-c410b206-7118-4087-8440-bb096528658f
> Record changed: 2026-10-13

# Fate Therapeutics

Headquarters country

United States

Source: [search.gleif.org](https://search.gleif.org/#/record/549300L14Q4UHOODLA90)

Registry sponsor category

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/)

## Names and classification

**Other names**

- Fate Therapeutics

**Company name**

Fate Therapeutics

**Organisation type**

Industry

**Registered legal name**

Fate Therapeutics, Inc.

Source: [search.gleif.org](https://search.gleif.org/#/record/549300L14Q4UHOODLA90)

**US industry code (SIC)**

Biological products, (no disgnostic substances)

Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001434316)

**Registry sponsor category**

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/)

## Location and listing

**Headquarters country**

United States

Source: [search.gleif.org](https://search.gleif.org/#/record/549300L14Q4UHOODLA90)

**Publicly traded (proxy)**

Yes

**Listing at source**

Listed

## Identifiers

**SEC filer number (CIK)**

0001434316

Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001434316)

**Legal Entity Identifier (LEI)**

549300L14Q4UHOODLA90

Source: [search.gleif.org](https://search.gleif.org/#/record/549300L14Q4UHOODLA90)

## Related records

### Trials (25)

- [A Phase 1 Study of FT819 in B-cell Mediated Autoimmune Disease](https://trialight.com/data/trial/a-phase-1-study-of-ft819-in-b-cell-mediated-autoimmune-6b8b0d2c-15f0-4af3-a304-bbce1760f628.md)
- A Phase 1 Trial of a Single ProHema® CB Product for Pediatric Patients With Hematologic Malignancies
- A Phase 2, Open-Label, Single-Arm Trial of FT819 in Participants With Lupus Nephritis
- A Trial of a Single ProHema-CB Product Transplant in Pediatric Patients With Inherited Metabolic Disorders
- FATE-NK100 as Monotherapy and in Combination With Monoclonal Antibody in Subjects With Advanced Solid Tumors
- First-in Cancer-Type Phase I Study of FT536 for Recurrent WHO Grade 4 Astrocytoma
- FT500 as Monotherapy and in Combination With Immune Checkpoint Inhibitors in Subjects With Advanced Solid Tumors
- FT516 in Combination With Monoclonal Antibodies in Advanced Solid Tumors
- FT516 in Subjects With Advanced Hematologic Malignancies
- FT522 With Rituximab in Relapsed/Refractory B-Cell Lymphoma (FT522-101)
- FT536 Monotherapy and in Combination With Monoclonal Antibodies in Advanced Solid Tumors
- FT538 in Combination With Monoclonal Antibodies in Advanced Solid Tumors
- FT538 in Subjects With Advanced Hematologic Malignancies
- FT576 in Subjects With Multiple Myeloma
- FT596 as a Monotherapy and in Combination With Anti-CD20 Monoclonal Antibodies
- FT596 in Combination With R-CHOP in Subjects With B-Cell Lymphoma
- FT819 in Subjects With B-cell Malignancies
- [FT825/ONO-8250, an Off-the-Shelf, HER2 CAR-T, With or Without Monoclonal Antibodies in Advanced Solid Tumors](https://trialight.com/data/trial/ft825-ono-8250-an-off-the-shelf-her2-car-t-with-or-without-1027adda-8254-417f-ac37-ff1509e170af.md)
- FT836 With or Without Chemotherapy and/or Monoclonal Antibodies, in Participants With Advanced Solid Tumors
- Long-term Follow-Up Study Following Treatment With Fate Therapeutics' Engineered Cellular Immunotherapy

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