Clin2
NCT07771361Possibly a fitNot yet recruiting

BAFF CAR-T cells for relapsed or refractory lymphoma and multiple myeloma

Non-Hodgkin Lymphoma Refractory/ RelapsedMultiple Myeloma RefractoryMultiple Myeloma in RelapseNon-Hodgkin Lymphoma, B-cellNon-Hodgkin LymphomaNon-Hodgkin Lymphoma (NHL)Multiple Myeloma (MM), Lymphoma, Large B-Cell, Diffuse (DLBCL), LymphomaMultiple Myeloma in Remission

Part of Blood & lymphatic, Cancer, Heart & circulation, Immune system & allergy clinical trials.

This trial tests a new treatment called BAFF CAR-T cells (LMY-920) for people with certain types of lymphoma or multiple myeloma that have come back or not responded to previous treatments. The therapy uses your own immune cells, modified to attack cancer cells, and may offer a new option when standard treatments have not worked.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
90 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have a type of B-cell lymphoma (like diffuse large B-cell, follicular, mantle cell, or others) that has returned after at least 2 prior treatments, or that did not respond to your last chemotherapy.
  • Or you have multiple myeloma that has returned or not responded after at least 3 prior treatments (including an immunomodulatory drug, a proteasome inhibitor, and an anti-CD38 antibody).
  • You are 18 years or older.
  • You are generally able to care for yourself (ECOG performance status of 0, 1, or 2).
  • You have at least one measurable tumor or lesion.
  • You do not have lymphoma or leukemia that has spread to the brain or spinal cord.
  • You have adequate organ function (heart, lungs, liver, kidneys).
  • If you are of childbearing potential, you agree to use effective birth control for at least 6 months after the infusion.
  • You have not had certain types of transplants or have no active graft-versus-host disease.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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