OncoMatch/Clinical Trials/NCT07030699
A Study of Epcoritamab With Lenalidomide and Tafasitamab in People With Diffuse Large B Cell Lymphoma
Is NCT07030699 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Epcoritamab and Lenalidomide for lymphoma.
Treatment: Epcoritamab · Lenalidomide · Tafasitamab — The researchers are doing this study to find out whether the combination of epcoritamab with tafasitamab and lenalidomide is a safe and effective treatment for relapsed or refractory DLBCL. This is the first time the combination of drugs is being tested.
Check if I qualifyExtracted eligibility criteria
Cancer type
Non-Hodgkin Lymphoma
Biomarker criteria
Required: MS4A1 overexpression (CD20+)
histologically confirmed CD20+ lymphoma as documented in the most recent representative pathology report
Required: CD19 expression (CD19+ (only required if prior anti-CD19 therapy))
Patients treated with prior anti-CD19 therapy must have confirmation of CD19 expression in a biopsy done after progression on the last CD19 directed therapy
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Must have received: systemic therapy
At least 2 prior lines of systemic therapy including CART or ASCT (up to 4 prior lines of therapy allowed)
Cannot have received: CD3/CD20 bispecific antibody
Exception: Allowed if received as part of frontline therapy for DLBCL and in remission ≥1 year post frontline therapy; or as bridging therapy prior to CAR-T without refractory/progressive disease on BiAb; or in remission ≥6 months after last dose
Prior CD3/CD20 BiAb based therapy with the following exceptions
Cannot have received: tafasitamab (tafasitamab)
Exception: Allowed if received as part of frontline therapy for DLBCL and in remission ≥1 year post frontline therapy; or prior lenalidomide without intolerance or progression
Prior tafasitamab and/or lenalidomide therapy for lymphoma
Cannot have received: lenalidomide (lenalidomide)
Exception: Allowed if received as part of frontline therapy for DLBCL and in remission ≥1 year post frontline therapy; or prior lenalidomide without intolerance or progression
Prior tafasitamab and/or lenalidomide therapy for lymphoma
Cannot have received: allogeneic stem cell transplantation
Prior allogeneic stem cell transplantation
Cannot have received: solid organ transplantation
Prior solid organ transplantation
Lab requirements
Blood counts
Hemoglobin ≥8 g/dL (red blood cell transfusions are allowed); ANC ≥1,000/mm^3 or ≥500/mm^3 if due to disease involvement in the bone marrow (G-CSF use is allowed); Platelet count ≥75,000 cells/mm^3 or ≥50,000/mm^3 if due to disease involvement in the bone marrow (platelets transfusions are allowed)
Kidney function
Estimated Creatinine Clearance (CrCl) ≥40 mL/min (Cockcroft-Gault formula or other institutional standard methods)
Liver function
Serum aspartate transaminase (AST) or alanine transaminase (ALT) ≤2.5 x ULN; Direct bilirubin ≤ 2 x ULN (≤3 if due to Gilbert's syndrome or liver involvement by the lymphoma)
Must have adequate organ and marrow status Hemoglobin ≥8 g/dL (red blood cell transfusions are allowed) Absolute neutrophil count (ANC) ≥1,000/mm^3 or ≥500/mm^3 if due to disease involvement in the bone marrow (G-CSF use is allowed). Platelet count ≥75,000 cells/mm^3 or ≥50,000/mm^3 if due to disease involvement in the bone marrow (platelets transfusions are allowed) Estimated Creatinine Clearance (CrCl) ≥40 mL/min (Cockcroft-Gault formula or other institutional standard methods) Serum aspartate transaminase (AST) or alanine transaminase (ALT) ≤2.5 x upper limit of normal (ULN) Direct bilirubin ≤ 2 x ULN (≤3 if due to Gilbert's syndrome or liver involvement by the lymphoma)
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Memorial Sloan Kettering Basking Ridge (All Protocol Activities) · Basking Ridge, New Jersey
- Memorial Sloan Kettering Monmouth (All Protocol Activities) · Middletown, New Jersey
- Memorial Sloan Kettering Bergen (All Protocol Activities) · Montvale, New Jersey
- Memorial Sloan Kettering Cancer Center Suffolk - Commack (All Protocol Activities) · Commack, New York
- Memorial Sloan Kettering Westchester (All Protocol Activities) · Harrison, New York
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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