CD30 CAR T Cells for Relapsed Lymphoma (RELY-30)

This study is testing a treatment called CD30 CAR T Cells for people aged 12 to 75 with Hodgkin's Lymphoma or Non-Hodgkin Lymphoma that has come back or not responded to previous treatments. The treatment uses your own infection-fighting T cells, which are specially trained in a lab to recognize and kill lymphoma cells that have a marker called CD30. Researchers will give you one infusion of these modified T cells. The main goal is to see how safe the treatment is by monitoring for side effects (dose-limiting toxicities) for 6 weeks. You must have CD30 positive tumor cells to be eligible.

Study design
This is an interventional study with a planned enrollment of 60 participants. It is a dose escalation study, meaning participants will start at one of three different dose levels of CD30 CAR T Cells.
What's involved
You will have blood drawn, or undergo a procedure called apheresis to collect your T cells. You will receive one infusion of the modified T cells.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint for safety is measured at 6 weeks after treatment.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT02917083

CD30 CAR T Cells, Relapsed CD30 Expressing Lymphoma (RELY-30)

Recruiting
PHASE1Ages 12–75InterventionalTreatment
Baylor College of Medicine
~60 participants
Updated 2026-06-10 on ClinicalTrials.gov
What's tested:CAR T Cells

At a glance

Recruiting sites
2 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of Patients with Dose-Limiting Toxicities (DLT)
Measured over 6 weeks
Hodgkin's Lymphoma
Non-Hodgkin Lymphoma
2 sites across 1 states
Texas2
  • Carlos A Ramos, MD · PRINCIPAL_INVESTIGATOR · Baylor College of Medicine

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  • Number of Patients with Dose-Limiting Toxicities (DLT)6 weeks

    Each treated patient will be followed for 6 weeks post the T-cell infusion for the evaluation of DLTs.