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Study identifier: NCT06828991 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Evaluate the Impact of Mosunetuzumab Consolidation for Older Patients With Diffuse Large B-cell Lymphoma (DLBCL) Who Have Detectable Amounts of ctDNA (Circulating Tumor DNA) at the End of Treatment With Pola-R-mini-CHP

Condition: Diffuse Large B-Cell Lymphoma (DLBCL)  ·  Sponsor: Danielle Wallace

PhasePhase 2
Planned participants40
Who can joinAll sexes, 70 Years to no upper limit
Healthy volunteersNo

About this study

Older patients with diffuse large B- cell lymphoma (DLBCL) do not have the same rates of disease control as younger patients and are at risk for toxicity. Identifying which patients might benefit from more therapy at the end of first-line treatment is important. The ability to measure small amounts of persistent lymphoma (circulating tumor DNA or ctDNA) might allow the investigators to risk stratify patients. If older patients have detectable ctDNA in the blood at the end of six cycles of polatuzumab vedotin, rituximab and dose-attentuated CHP chemotherapy, patients will receive a bispecific antibody called mosunetuzumab. The investigators hypothesize this will result in "clearing" the ctDNA from the blood and result in better disease control and outcomes for patients. The study will also measure the safety of this regimen and the impact on the function of these older patients utilizing a tool called the geriatric assessment.

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

Talk to the study team

Danielle Wallace, MD  ·  585-273-5761  ·  danielle_wallace@urmc.rochester.edu

Clinical Trials Office  ·  wcictoresearch@urmc.rochester.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Wilmot Cancer InstituteRochester, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06828991