FT819
DrugExperimental Interventional Therapy
NCT Number: NCT04629729
This is a Phase I dose-finding study of FT819 as monotherapy and in combination with IL-2 in subjects with relapsed/refractory B-cell Lymphoma, Chronic Lymphocytic Leukemia and Precursor B-cell Acute Lymphoblastic Leukemia. The study will consist of a dose-escalation stage and an expansion stage where participants will be enrolled into indication-specific cohorts.
This study is active but is not currently recruiting participants.
18 year and older
All sexes
Interventional
Phase 1
University of Alabama at Birmingham, Birmingham, Alabama, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Diagnosis of B-cell lymphoma, CLL or B-ALL as described below:
B-Cell Lymphoma:
Chronic Lymphocytic Leukemia (CLL):
Precursor B-cell Acute Lymphocytic Leukemia (B-ALL):
ALL SUBJECTS:
Key Exclusion Criteria:
ALL SUBJECTS:
Experimental Interventional Therapy
Lympho-conditioning agent
Lympho-conditioning agent
Other names: Fludara
Biologic response modifier
Other names: Interleukin-2
Lympho-conditioning agent
Other names: Bendeka, Treanda
Time frame: Up to Day 29
Time frame: Up to 15 years
Time frame: Up to approximately 2 years after last dose of FT819
Time frame: Up to 15 years
Time frame: Up to 15 years
Time frame: Up to 15 years
Time frame: Up to 15 years
Time frame: Study Days 1, 2, 3, 4, 5, 8, 11, 15, 22, and 29
The PK of FT819 in peripheral blood will be reported as the relative percentage of product (FT819) DNA versus patient DNA (% chimerism) measured from blood samples at the specified time points
Time frame: Up to 15 years
Fate Therapeutics
Industry
A Phase I Study of FT819 in Subjects With B-cell Malignancies
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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