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FT596 in Combination With R-CHOP in Subjects With B-Cell Lymphoma

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Fate Therapeutics

Status and phase

Withdrawn
Phase 1

Conditions

Transformed Indolent Non-Hodgkin's Lymphoma
Marginal Zone Lymphoma
Mantle Cell Lymphoma
Follicular Lymphoma
Diffuse Large B Cell Lymphoma

Treatments

Drug: Rituximab
Drug: Cyclophosphamide
Drug: FT596
Drug: Vincristine
Drug: Doxorubicin
Drug: Prednisone
Drug: Bendamustine

Study type

Interventional

Funder types

Industry

Identifiers

NCT05934097
FT596-102

Details and patient eligibility

About

This is a Phase I study of FT596 in combination with two different schedules (standard or alternate) of R-CHOP in subjects with B-cell lymphoma who are previously untreated or have received no more than one prior line of treatment. The study will consist of a dose-escalation stage followed by a dose-expansion stage.

Full description

This is a Phase I study of FT596 in combination with 2 different schedules (standard or alternate) of R-CHOP in subjects with B-cell lymphoma who are previously untreated or have received no more than one prior line of treatment.

The study will evaluate both the clinical benefit of FT596 when combined with R-CHOP given on a standard or alternate schedule.

Subjects will be enrolled in two stages: a dose-escalation stage and a dose-expansion stage. After safety and tolerability have been assessed to define the maximum tolerated dose (MTD) (or the maximum assessed dose [MAD] in the absence of dose limiting toxicities [DLTs] defining the MTD) in the dose-escalation stage, the dose-expansion stage will further evaluate the safety and activity of FT596 in combination.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria:

  • Diagnosis of B-cell lymphoma (BCL) as described below:

    • Histologically documented BCL
    • Previously untreated or no more than one prior systemic therapy for BCL
    • At least one bi-dimensionally measurable lesion
    • Subjects with >1 measurable lesion agreement to undergo a biopsy
  • Capable of giving signed informed consent

  • Age ≥ 18 years old

  • Stated willingness to comply with study procedures through study duration

  • Contraception use for women and men as defined in the protocol

  • Negative serum pregnancy test within 7 days of treatment for women

Key Exclusion Criteria:

  • Prior anthracycline therapy
  • Females who are pregnant or breastfeeding
  • Eastern Cooperative Oncology Group (ECOG) Performance Status ≥2
  • Evidence of insufficient organ function
  • Currently receiving or likely to receive systemic immunosuppressive therapy
  • Receipt of 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 HIV test
  • Positive Hepatitis B (HBV) or Hepatitis C (HCV) test
  • Live vaccine <6 weeks prior to start of conditioning
  • Allergy to human albumin or dimethyl sulfoxide (DMSO)

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Regimen A (FT596 in combination with standard schedule R-CHOP)
Experimental group
Description:
FT596 in combination with standard schedule R-CHOP (rituximab, cyclophosphamide, doxorubicin, and vincristine on Day 1; prednisone on Days 1-5; and FT596 on Day 8) for a total of six 21-day cycles.
Treatment:
Drug: Rituximab
Drug: Doxorubicin
Drug: Bendamustine
Drug: Prednisone
Drug: Cyclophosphamide
Drug: Vincristine
Drug: FT596
Regimen B (FT596 in combination with alternate schedule R-CHOP)
Experimental group
Description:
FT596 in combination with alternate schedule R-CHOP (prednisone on Days 1-5; rituximab, cyclophosphamide, doxorubicin, and vincristine on Day 5; and FT596 on Day 8) for a total of six 21-day cycles
Treatment:
Drug: Rituximab
Drug: Doxorubicin
Drug: Bendamustine
Drug: Prednisone
Drug: Cyclophosphamide
Drug: Vincristine
Drug: FT596

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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