Clin2
NCT05801913Possibly a fitRecruiting

Personalized immune cell therapy plus a CMV vaccine

High Grade B-Cell Non-Hodgkin's LymphomaIntermediate Grade B-Cell Non-Hodgkin's LymphomaRecurrent B-Cell Non-Hodgkin LymphomaRefractory B-Cell Non-Hodgkin Lymphoma

Treatments studied

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

This Phase 1 study tests genetically modified immune cells (made from your own blood) plus a vaccine aimed at controlling CMV-related lymphoma. It’s for adults with intermediate or high-grade B-cell non-Hodgkin lymphoma who can’t get (or don’t want) certain standard stem-cell transplant options.

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

Phase
Phase 1
Enrollment
15 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • Be at least 18 years old and able to give consent (or have a legal representative).
  • Have intermediate or high-grade B-cell non-Hodgkin lymphoma that is CD19-positive, and be in a relapsed or refractory situation where you cannot/choose not to use autologous stem-cell transplant.
  • Be CMV-positive on blood testing.
  • Be well enough for treatment: life expectancy of at least 16 weeks, KPS score 70 or higher, and enough blood counts (neutrophils, hemoglobin, and platelets).
  • Have organ function tests within limits (kidney, liver, and heart function) and no need for extra oxygen to keep saturation above 92%.
  • Be able to undergo leukapheresis and later treatments (including lymphodepleting chemotherapy, steroids, and tocilizumab) with no known contraindications; also avoid certain medicines or infections at enrollment.

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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