FT596 as a Monotherapy and in Combination With Anti-CD20 Monoclonal Antibodies
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- Fate Therapeutics
- Study ID
- NCT04245722
- Phase
- PHASE1
- Status
- Terminated
Conditions
- Chronic Lymphocytic Leukemia
- Lymphoma, B-Cell
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- FT596 — DRUGExperimental Interventional Therapy
- Cyclophosphamide — DRUGLympho-conditioning agent
- Fludarabine — DRUGLympho-conditioning agent
- Rituximab — DRUGMonoclonal Antibody
- Obinutuzumab — DRUGMonoclonal Antibody
- Bendamustine — DRUGConditioning agent
Study Details
This is a Phase I dose-finding study of FT596 as monotherapy and in combination with Rituximab or Obinutuzumab in subjects with relapsed/refractory B-cell Lymphoma or Chronic Lymphocytic Leukemia. The study will consist of a dose-escalation stage and an expansion stage where participants will be enrolled into indication-specific cohorts.
Key Dates
- Start date
- Mar 19, 2020
- Status verified
- Oct 2023
- Primary completion
- Sep 27, 2023
- Completion
- Sep 27, 2023
Study Design
- Enrollment
- 98 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: FT596 Monotherapy, LymphomaFT596 monotherapy in adult subjects with r/r B-cell Lymphoma
- Experimental: FT596 in Combination with Rituximab, LymphomaFT596 in combination with Rituximab in adult subjects with r/r B-cell Lymphoma
- Experimental: FT596 in Combination with Obinutuzumab, LymphomaFT596 in combination with Obinutuzumab in adult subjects with r/r B-cell Lymphoma
- Experimental: FT596 Monotherapy, CLLFT596 monotherapy in adult subjects with r/r CLL
- Experimental: FT596 in Combination with Obinutuzumab, CLLFT596 in combination with Obinutuzumab in adult subjects with r/r CLL
Primary Outcome Measure
Incidence of dose-limiting toxicities within each dose level cohort [ Time Frame: Day 29 ]
Locations (9)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The University of Chicago | Chicago | Illinois | 60637 | - |
| University of Minnesota Masonic Cancer Center | Minneapolis | Minnesota | 55455 | - |
| Washington University School of Medicine | St Louis | Missouri | 63110 | - |
| Memorial Sloan Kettering Cancer Center | New York | New York | 10065 | - |
| NYU Langone Health | New York | New York | 10016 | - |
| Sarah Cannon Research Institute (Tennessee Oncology) | Nashville | Tennessee | 37203 | - |
| MD Anderson Cancer Center | Houston | Texas | 77030 | - |
| SCRI-TTI | San Antonio | Texas | 78229 | - |
| Swedish Cancer Institute | Seattle | Washington | 98104 | - |
Find similar trials in Chicago, IL
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The University of Chicago· Chicago, ILUniversity of Minnesota Masonic Cancer Center· Minneapolis, MNWashington University School of Medicine· St Louis, MOMemorial Sloan Kettering Cancer Center· New York, NYNYU Langone Health· New York, NYSarah Cannon Research Institute (Tennessee Oncology)· Nashville, TN
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