A Study of Epcoritamab With Lenalidomide and Tafasitamab in People With Diffuse Large B Cell Lymp… (NCT07030699) | Clinical Trial Compass
WithdrawnPhase 2
A Study of Epcoritamab With Lenalidomide and Tafasitamab in People With Diffuse Large B Cell Lymphoma
Stopped: Lack of accrual
0Started 2025-08-13
Plain-language summary
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.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Age ≥ 18 years
* Pathologically confirmed diffuse large B cell lymphoma, transformed indolent lymphoma, primary mediastinal B cell lymphoma, high grade B cell lymphoma, follicular lymphoma grade 3B
* Subjects must have histologically confirmed CD20+ lymphoma as documented in the most recent representative pathology report.
* Presence of CD19 is not required to be confirmed (except if patients have received anti-CD19 therapy in the past). 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.
* At least 2 prior lines of systemic therapy including CART or ASCT (up to 4 prior lines of therapy allowed). Note that bridging therapy prior to ASCT or CART will be counted as a separate line of therapy)
* At least one prior line of systemic therapy for patients ineligible for ASCT/CART or patients unwilling to undergo CAR-T/ASCT for logistic or other reasons (up to 4 prior lines of therapy allowed)
* Have radiologically measurable lymphadenopathy or extranodal involvement.
* Eastern Cooperative Oncology Group performance status (PS) ≤ 2 (ECOG \>2 can be enrolled if PS compromised from lymphoma e.g. spinal cord compression and expected to improve rapidly with therapy)
* 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 involvemen…