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Recruiting Phase 2 NCT06919939

Epcoritamab in Combination With Loncastuximab Tesirine in Relapsed/Refractory Large B-cell Lymphoma

Trial Parameters

Condition Large B-cell Lymphoma
Sponsor University of Miami
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 26
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2026-01-07
Completion 2031-01-07
Interventions
EpcoritamabLoncastuximab Tesirine

Brief Summary

The purpose of this study is to determine whether combining Loncastuximab Tesirine with Epcoritamab is tolerable and effective for reducing and/or eliminating lymphoma cells in the body.

Eligibility Criteria

Inclusion Criteria: 1. Men and women aged 18 years or older at the time of signing informed consent. 2. Able and willing to sign the informed consent form (ICF). 3. Ability to comply with the trial protocol. 4. Relapsed/refractory (r/r) large B-cell lymphoma (LBCL) as determined by the local hematopathology laboratory from the following diagnoses by 2016 World Health Organization (WHO) classification of lymphoid neoplasms (Swerdlow et al., 2016): 1. LBCL or DLBCL, not otherwise specified (NOS) 2. High-grade B-cell lymphoma (NOS or double/triple hit \[technically classified in WHO 2016 as high-grade B-cell lymphoma (HGBCL), with Myc and B-cell lymphoma 2 (BCL2) and/or B-cell lymphoma 6 (BCL6) translocations\]) 3. Transformed from follicular lymphoma, marginal zone lymphoma (MZL), and nodular lymphocyte predominant Hodgkin lymphoma 4. Follicular lymphoma stage 3B 5. Primary mediastinal B-cell lymphoma previously treated with checkpoint inhibitor Note: Relapsed disease is defined as disea

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