A Study of Mosunetuzumab for Older Patients with DLBCL
This study is for older patients (70 years or older) with Diffuse Large B-cell Lymphoma (DLBCL), a type of cancer. It's looking at whether an immunotherapy drug called mosunetuzumab can help patients who still have small amounts of lymphoma DNA (called circulating tumor DNA or ctDNA) in their blood after their initial treatment with Pola-R-mini-CHP. If you have detectable ctDNA and your PET/CT scan shows your cancer is in complete remission, you might receive mosunetuzumab for 6 cycles. Researchers hope this will clear the ctDNA and lead to better outcomes. The main goal is to see how many patients clear their ctDNA after mosunetuzumab treatment, measured over 18 weeks. The study plans to enroll 40 participants, but its current status is unclear.
- Study design
- This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 40 participants.
- What's involved
- If eligible, you would receive mosunetuzumab consolidation therapy for 6 cycles, with specific dosing on Day 1, Day 8, Day 15, and subsequent cycles. You would also have blood tests to check for ctDNA.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary outcome, ctDNA clearance, is measured from the beginning to the end of mosunetuzumab treatment at 18 weeks.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
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
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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What this trial measures
- ctDNA clearance rate after mosunetuzumab treatmentFrom the beginning to the end of mosunetuzumab treatment at 18 weeks
The primary endpoint of the trial is the ctDNA clearance rate after mosunetuzumab treatment among the subset of patients in a PET/CT CR but with ctDNA+ at the end of 6 cycles of R-pola-mini-CHP. The rate will be calculated as the number of subjects ctDNA- after mosunetuzumab treatment among all patients treated with mosunetuzumab as part of the Fleming two-stage design.