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OncoMatch/Clinical Trials/NCT06414148

MRD-Directed Consolidation With Epcor-only or Epcor-R2 Post Anti-CD19 CAR TCell Therapy for Large B-Cell Lymphoma

Is NCT06414148 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Epcoritamab and Epcoritamab, lenalidomide and rituximab for relapsed/refractory large b-cell lymphoma.

Phase 2RecruitingPeter MacCallum Cancer Centre, AustraliaNCT06414148Data as of May 2026

Treatment: Epcoritamab · Epcoritamab, lenalidomide and rituximabThis is a Phase II open-label, two-arm randomised non-comparative, multi-centre study to evaluate the efficacy of Epcor-only (Epcoritamab alone) or Epcor-R2 (Epcoritamab, lenalidomide and rituximab) as consolidation post anti-CD19 CAR T-cell therapy for patients that have responded by conventional criteria but who are at high risk of progression by virtue of being Minimal Residual Disease (MRD) positive as determined by a Circulating Tumour DNA (ctDNA) assay.

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Extracted eligibility criteria

Cancer type

Diffuse Large B-Cell Lymphoma

Non-Hodgkin Lymphoma

Biomarker criteria

Required: CD19 CAR T-cell therapy received

Received...anti-CD19 CAR T-cell therapy as the most recent large B-cell lymphoma treatment

Excluded: CD20 negative

Patients whose lymphoma is known to be CD20 negative on the most recent biopsy prior to CAR T-cell therapy

Performance status

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

Prior therapy

Must have received: anti-CD19 CAR-T cell therapy — most recent large B-cell lymphoma treatment

Received...anti-CD19 CAR T-cell therapy as the most recent large B-cell lymphoma treatment

Cannot have received: bispecific antibody targeting CD3 and CD20

Progression or relapse within 3 months after a regimen containing a bispecific antibody targeting CD3 and CD20

Lab requirements

Blood counts

Adequate haematological function documented within 7 days prior to randomisation

Kidney function

Adequate renal function, documented within 7 days prior to randomisation

Liver function

Adequate hepatic function documented within 7 days prior to randomisation

Cardiac function

Adequate cardiac function

Adequate haematological function documented within 7 days prior to randomisation; Adequate cardiac function; Adequate renal function, documented within 7 days prior to randomisation; Adequate hepatic function documented within 7 days prior to randomisation

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

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