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OncoMatch/Clinical Trials/NCT06050694

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

Is NCT06050694 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies glofitamab for diffuse large b cell lymphoma (dlbcl).

Phase 2RecruitingUniversity Health Network, TorontoNCT06050694Data as of Jun 2026Location: Canada

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

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Extracted eligibility criteria

Treatments studied

Immunotherapy

glofitamab

Cancer type

Diffuse Large B-Cell Lymphoma

Non-Hodgkin Lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: anthracycline

Prior exposure to any anthracycline

Cannot have received: anti-CD20 antibody (rituximab)

Prior exposure to...rituximab

Cannot have received: CD3-targeted bispecific antibody

Prior exposure to...cluster of differentiation 3 (CD3) targeted bispecific antibody

Lab requirements

Blood counts

Absolute Neutrophil Count (ANC) <1.0 x10^9/L (subjects with bone marrow involvement by lymphoma are eligible regardless of ANC); Hemoglobin (Hgb) ≤ 9 g/dL; Platelets <50 x10^9/L (subjects with bone marrow involvement by lymphoma are eligible regardless of platelet count)

Kidney function

Creatinine clearance <30 mL/min

Liver function

Total serum bilirubin >2 times the upper limit of normal (or <3 times for Gilbert's disease or documented hepatic involvement by lymphoma), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) >3 times the upper limit of normal (or >5 times for documented hepatic involvement by lymphoma)

Cardiac function

Left ventricular ejection fraction (LVEF) ≥ 50%, as determined on cardiac multiple-gated acquisition (MUGA) scan or cardiac echocardiogram (ECHO)

Left ventricular ejection fraction (LVEF) ≥ 50%... Absolute Neutrophil Count (ANC) <1.0 x10^9/L... Hemoglobin (Hgb) ≤ 9 g/dL... Platelets <50 x10^9/L... Total serum bilirubin >2 times the upper limit of normal (or <3 times for Gilbert's disease or documented hepatic involvement by lymphoma), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) >3 times the upper limit of normal (or >5 times for documented hepatic involvement by lymphoma)... Creatinine clearance <30 mL/min.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06050694 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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