Cema-cel for Large B-cell Lymphoma with Minimal Residual Disease

This study is for adults with Large B-cell Lymphoma (LBCL) who have finished their first treatment and still have a small amount of cancer cells, called minimal residual disease (MRD). You would have completed standard first-line therapy (like R-CHOP) and have MRD detected by a special test. The study is testing a new cell therapy called cemacabtagene ansegedleucel (cema-cel), which is a type of CAR T-cell therapy. This therapy uses your own immune cells to fight cancer. Researchers want to see if cema-cel, given after a short chemotherapy (fludarabine and cyclophosphamide), is better than just watching to prevent the cancer from returning. The main goal is to see how long people live without their cancer coming back, for up to 60 months. The study plans to enroll 250 participants, but its current status is unclear.

Study design
This is a randomized, open-label study involving 250 participants. You would be randomly assigned to either receive cema-cel treatment or be in an observation group.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for up to 60 months to see how long they live without their cancer returning.

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NCT06500273

Consolidation of First-Line MRD+ Remission With Cema-cel in Patients With LBCL

Recruiting
PHASE2Ages 18+InterventionalTreatment
Allogene Therapeutics
~250 participants
Updated 2026-08-31 on ClinicalTrials.gov
What's tested:cemacabtagene ansegedleucelFludarabineCyclophosphamideForesight CLARITY™ IUO MRD test, powered by PhasED-Seq™

At a glance

Recruiting sites
82 of 83 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Event-free survival per independent review committee assessment
Measured over Up to 60 months
Large B-cell Lymphoma
83 sites across 40 states
California7
Texas5
Seoul5
Florida4
Indiana3
Kentucky3
Missouri3
New Jersey3
  • Allogene Study Director · STUDY_DIRECTOR · Allogene Therapeutics, Inc.

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  • Event-free survival per independent review committee assessmentUp to 60 months