RecruitingPhase 2NCT06050694

Feasibility Trial of Glofitamab in a Response Adapted Approach Incorporating Interim FDG PET and ctDNA to Optimize Primary Therapy of DLBCL (GRAIL)

Feasibility Trial of Glofitamab in a Response Adapted Approach Incorporating Interim FDG PET and ctDNA to Optimize Primary Therapy of DLBCL


Sponsor

University Health Network, Toronto

Enrollment

40 participants

Start Date

Jan 24, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a phase ll study of participants with untreated diffuse large B Cell lymphoma (DLBCL).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a new treatment strategy for diffuse large B-cell lymphoma (DLBCL), an aggressive blood cancer. It starts with standard chemotherapy and uses interim PET scans and blood tests to decide whether to add an additional immunotherapy drug (glofitamab) to improve outcomes. **You may be eligible if...** - You are 18 or older and have been diagnosed with DLBCL or a related aggressive B-cell lymphoma - You have not previously been treated for DLBCL - You are considered eligible for full-dose chemotherapy by your oncologist - You are in good enough overall health to undergo intensive treatment **You may NOT be eligible if...** - You have received prior treatment for DLBCL - You have significant heart, liver, kidney, or lung problems - You have active infections including hepatitis B, hepatitis C, or HIV - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGglofitamab

Glofitamab 2.5 mg Cycle 3 Day 8 and 10 mg on Day 15 Cycles 3-6


Locations(3)

Princess Margaret Cancer Centre

Toronto, Ontario, Canada

Princess Margaret Cancer Centre

Toronto, Ontario, Canada

Jewish General Hospital

Montreal, Quebec, Canada

View Full Details on ClinicalTrials.gov

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NCT06050694


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