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Active, Not Recruiting

NCT Number: NCT04629729

FT819 in Subjects With B-cell Malignancies

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Who can participate

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:

  • Histologically documented lymphomas expected to express CD19
  • Relapsed/refractory disease following at least 2 prior lines of multi-agent immunochemotherapy

Chronic Lymphocytic Leukemia (CLL):

  • Diagnosis of CLL per iwCLL guidelines
  • Relapsed/refractory disease following at least two prior systemic treatment regimens

Precursor B-cell Acute Lymphocytic Leukemia (B-ALL):

  • Diagnosis of B-ALL by flow cytometry, bone marrow histology, and/or cytogenetics
  • Relapsed/refractory disease after at least 2 cycles of standard multiagent induction chemotherapy. For subjects with Philadelphia-chromosome positive (Ph+) disease, failure or intolerance to a tyrosine kinase inhibitor therapy-containing regimen

ALL SUBJECTS:

  • Capable of giving signed informed consent
  • Age ≥ 18 years old
  • Stated willingness to comply with study procedures and duration
  • Contraceptive use for women and men as defined in the protocol

Key Exclusion Criteria:

ALL SUBJECTS:

  • Females who are pregnant or breastfeeding
  • Eastern Cooperative Oncology Group (ECOG) Performance Status ≥2
  • Body weight <50 kg
  • Evidence of insufficient organ function
  • Receipt of therapy within 2 weeks prior to Day 1 or five half-lives, whichever is shorter; or any investigational therapy within 28 days prior to Day 1
  • Currently receiving or likely to require systemic immunosuppressive therapy
  • Ongoing requirement for systemic GvHD therapy following prior allogeneic hematopoietic stem cell transplant (HSCT) or allogeneic CAR-T
  • Receipt of an allograft organ transplant
  • Known active central nervous system (CNS) involvement by malignancy
  • Non-malignant CNS disease such as stroke, epilepsy, CNS vasculitis, or neurodegenerative disease
  • Clinically significant cardiovascular disease
  • Positive serologic test results for HIV infection
  • Positive serologic and polymerase chain reaction (PCR) test results for Hepatitis B (HBV) infection
  • Positive serologic and PCR test results for Hepatitis C (HCV) infection
  • Live vaccine <6 weeks prior to start of lympho-conditioning
  • Known allergy to albumin (human) or DMSO

Treatment and study plan

FT819

Drug

Experimental Interventional Therapy

Cyclophosphamide

Drug

Lympho-conditioning agent

Fludarabine

Drug

Lympho-conditioning agent

Other names: Fludara

IL-2

Drug

Biologic response modifier

Other names: Interleukin-2

Bendamustine

Drug

Lympho-conditioning agent

Other names: Bendeka, Treanda

Primary outcomes

  1. Incidence and nature of dose-limiting toxicities within each dose level cohort

    Time frame: Up to Day 29

  2. Incidence, nature, and severity of adverse events (AEs) of FT819 as monotherapy and in combination with IL-2 in r/r B-cell lymphoma, r/r chronic lymphocytic leukemia, and r/r precursor B-cell acute lymphoblastic leukemia

    Time frame: Up to 15 years

Secondary outcomes

  1. Investigator-assessed objective-response rate (ORR)

    Time frame: Up to approximately 2 years after last dose of FT819

  2. For BCL and CLL Only: Investigator-assessed duration of objective response (DOR)

    Time frame: Up to 15 years

  3. For BCL and CLL Only: Investigator-assessed duration of complete response (DoCR)

    Time frame: Up to 15 years

  4. For BCL and CLL Only: Progression-free survival (PFS)

    Time frame: Up to 15 years

  5. Overall survival (OS)

    Time frame: Up to 15 years

  6. Determination of the pharmacokinetics of FT819 cells in peripheral blood.

    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

  7. For B-ALL Only: Investigator-assessed relapse-free survival (RFS)

    Time frame: Up to 15 years

Sponsors and collaborators

Lead sponsor

Fate Therapeutics

Industry

Registry information

Official study title

A Phase I Study of FT819 in Subjects With B-cell Malignancies

Important dates

Study start
2021
Primary completion
2025
Study completion
2039
First posted
Nov 16, 2020
Registry last updated
Mar 19, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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