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Study identifier: NCT05255354 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Optimizing ctDNA-based MRD Assessment in DLBCL, MCL, and FL Patients Undergoing CAR Therapy

Condition: Follicular Lymphoma · Diffuse Large B Cell Lymphoma · Mantle Cell Lymphoma  ·  Sponsor: Adaptive Biotechnologies

PhaseN/A
Planned participants300
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

In this study, invesigators propose to analyze 150 DLBCL patients, 50 MCL patients, and 100 FL patients to determine the clinical utility of ctDNA- as well as circulating tumor cell (CTC)-based MRD assessment in CAR therapy patients. The project detailed in this protocol will utilize the clonoSEQ platform as specific quantification of residual DLBCL/FL/MCL and correlate its results with radiologic assessment of disease and clinical outcomes. Invesitgators predict there will be a strong correlation between ctDNA and PET/CT and dynamic changes in ctDNA will precede radiologic evidence of disease recurrence in patients following CAR therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Heidi Simmons, PhD  ·  206-279-2591  ·  hsimmons@adaptivebiotech.com

Monica Gallucci  ·  mgallucci@adaptivebiotech.com

Always discuss trial participation with your own doctor first.

Locations (1)

Stanford Cancer CenterPalo Alto, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05255354