Phase 1 Study of JV-213 for Relapsed or Refractory B-cell Lymphomas

This study is testing a new cell therapy called JV-213 for adults with B-cell lymphomas that have come back or not responded to previous treatments (relapsed or refractory). JV-213 is a type of CAR T-cell therapy, which uses your own immune cells to fight cancer. Researchers want to find the safest and highest dose of JV-213 that can be given. They will also look at how well JV-213 works to shrink tumors and improve symptoms. You would receive JV-213 through an IV after a procedure called leukapheresis, which collects your immune cells. The study is currently recruiting participants.

Study design
This is an interventional study planning to enroll 33 participants. It is designed to find the highest tolerable dose of JV-213.
What's involved
You would undergo leukapheresis to collect your cells, and then receive JV-213 through an IV. You will be monitored for side effects and tumor response.
Compensation
Not stated in the trial record.
Follow-up
You will be monitored for adverse events through study completion, which is an average of 1 year.

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NCT05773040

A Phase 1 Study of JV-213 Autologous CD79b-targeting Chimeric Antigen Receptor T-cell Therapy in Adults With Relapsed or Refractory B-cell Lymphomas

Recruiting
PHASE1Ages 18+InterventionalTreatment
M.D. Anderson Cancer Center
~33 participants
Updated 2026-07-29 on ClinicalTrials.gov
What's tested:JV-213Leukapheresis

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5
Measured over through study completion; an average of 1 year
Lymphomas
B-cell Lymphomas
1 sites across 1 states
Texas1
  • Sattva Neelapu, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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  • Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5through study completion; an average of 1 year