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NCT Number: NCT05370430

BAFFR-targeting CAR T Cells for Patients With Relapsed or Refractory B-NHL

A Phase 1 Study Evaluating BAFFR-targeting CAR T Cells for Patients with Relapsed or Refractory B-cell Non-Hodgkin's Lymphoma (B-NHL)

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

City of Hope Medical Center, Duarte, California, United States

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About this study

This phase I trial evaluates the side effects and best dose of BAFFR-CAR T cells in treating patients with B-cell Non-Hodgkin's Lymphoma (B-NHL) that has come back (recurrent) or does not respond to treatment (refractory). T cells are infection fighting blood cells that can kill cancer cells. The T cells given in this study will come from the patient and will have a new gene put in them that makes them able to recognize BAFFR, a protein on the surface of cancer cells. These BAFFR-specific T cells may help the body's immune system identify and kill BAFFR+ cancer cells.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed Consent: Signed informed consent by the participant or legally authorized representative.
  • Age & Performance Status:
  • Age ≥ 18 years
  • ECOG performance status ≤ 2
  • Diagnosis & Disease Criteria:
  • Histologically confirmed B-NHL, including LBCL, MCL, and FL/MZL subtypes meeting specified prior treatment conditions.
  • BAFF-R expression on lymphoma cells required.
  • Measurable Disease: Tumor ≥1.5 cm on CT/PET scan or evidence of disease in blood, BM, GI, skin, or spleen.
  • Prior CAR T-cell Therapy: Allowed if ≥ 3 months since last treatment and CD19 CAR-T persistence < 5% before leukapheresis.
  • Organ Function & Laboratory Criteria:
  • Hematologic: ANC ≥ 1000/μL, Platelets ≥ 75,000/μL (exceptions for BM involvement).
  • Liver Function: Bilirubin ≤ 1.5x ULN (except Gilbert's), AST/ALT < 3x ULN.
  • Renal Function: CrCl ≥ 50 mL/min.
  • Cardiac & Pulmonary: LVEF ≥ 45%, QTcF ≤ 480 ms, O₂ saturation > 91% on room air.
  • Infectious Disease Screening: Seronegative for HIV, active HBV, active HCV (or undetectable viral load if positive).
  • Reproductive Considerations:
  • Negative pregnancy test for females of childbearing potential.
  • Use of effective contraception or abstinence through 3 months post-treatment.

Exclusion criteria

  • Prior Therapies & Transplants:
  • Prior allogeneic SCT.
  • Autologous SCT < 6 months before leukapheresis.
  • Concurrent systemic steroids or chronic immunosuppressant use.
  • Disease-Specific Exclusions:
  • Cardiac lymphoma involvement.
  • Need for urgent therapy due to tumor-related complications (e.g., bowel obstruction).
  • Medical Conditions:
  • Active autoimmune disease requiring immunosuppressants.
  • Primary immunodeficiency.
  • Cardiac conditions, including NYHA Class III/IV heart disease, arrhythmia, recent MI (≤ 6 months), stroke (≤ 6 months), or significant VTE (≤ 6 months).
  • Neurologic conditions, including prior optic neuritis, CNS inflammatory diseases, or seizure disorders.
  • History of malignancy, unless resected/treated with curative intent or in remission for ≥ 3 years.
  • Uncontrolled systemic infections or active CNS lymphoma.
  • Pregnancy & Breastfeeding: Females who are pregnant or nursing.
  • Other Considerations:
  • Investigator-determined safety concerns.
  • Potential noncompliance with study procedures.

Treatment and study plan

BAFFR-CAR T cells

Biological

First-in-human trial examining the safety and preliminary efficacy of BAFFR-CAR T cells in participants with r/r B-NHL

Primary outcomes

  1. Incidence of adverse events

    Time frame: Up to 1 year post treatment

    Assess the safety of administering BAFFR-CAR T cells in participants with relapsed or refractory (r/r) B-cell Non-Hodgkin's Lymphoma (B-NHL) and it's subtypes. Toxicity will be graded per Common Terminology Criteria for Adverse Events version 5.0, Cytokine Release Syndrome (CRS) and neurotoxicity which use the American Society for Transplantation and Cellular Therapy Consensus Criteria (ASTCT) and Graft versus Host Disease (GVHD) criteria. Toxicities will be followed from the start of lymphodepletion until the end of the study.

  2. Maximum Tolerated Dose (MTD)

    Time frame: The DLT evaluation period is defined as 28 days following BAFFR CAR-T infusion.

    Determine the maximum tolerated dose (MTD)/recommended Phase 2 dose (RP2D) of BAFFR-CAR T cells. The highest dose with ≤ 1/6 participants with DLT will be considered the MTD.

Secondary outcomes

  1. Disease Response

    Time frame: Up to 1 year post treatment

    Defined as achieving a best response of complete response or partial response per Lugano Criteria

  2. Minimal Residual Disease (MRD)

    Time frame: Up to 1 year post treatment

    Negative MRD is defined by malignant cells < 0.01% by flow cytometry or clonoSEQ.

  3. B Cell Quantification

    Time frame: Up to 1 year post treatment

    Measured by flow cytometry

  4. Progression-free survival (PFS)

    Time frame: From CAR T cell infusion to the first observation of disease relapse/progression or death from any cause, whichever occurs first, assessed up to 15 years.

    Kaplan-Meier product limit method with log-log transformation for the confidence interval will be used to estimate PFS.

  5. Overall Survival (OS)

    Time frame: From the day of BAFFR-CAR T cell infusion to death from any cause assessed, up to 15 years.

    Kaplan-Meier product limit method with log-log transformation for the confidence interval will be used to estimate OS.

Study contacts

Contact information is provided by the study sponsor or research team.

DeShaun Noakes, M.S.

CONTACT

[email protected]

760-533-4023

Hazel (Ting-Ying) Cheng, PhD

CONTACT

[email protected]

714-599-8077

Sponsors and collaborators

Lead sponsor

PeproMene Bio, Inc.

Industry

Collaborators

  • City of Hope Medical Center

Registry information

Official study title

A Phase 1 Study Evaluating BAFFR-targeting CAR T Cells for Patients With Relapsed or Refractory B-cell Non-Hodgkin's Lymphoma (B-NHL)

Important dates

Study start
2022
Primary completion
2027
Study completion
2028
First posted
May 11, 2022
Registry last updated
Nov 20, 2025

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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