About this trial
The purpose of this study is to find out whether the combination of epcoritamab and ibrutinib is a safe treatment approach that causes few or mild side effects in people with relapsed/refractory primary central nervous system lymphoma (PCNSL) or secondary central nervous system lymphoma (SCNSL).
Eligibility criteria
Qualifiers
>/= 18 years of age on the day of consenting to the study.
Histologically documented DLBCL at enrolling institution (biopsy or CSF samples in PCNSL; biopsy of CNS or non-CNS sample in SCNSL)
Participants must have an ECOG performance status of 0, 1, or 2.
Absolute neutrophil count (ANC) ≥ 1 x 109/L
Disqualifiers
Newly diagnosed PCNSLs or SCNSLs and patients with non-CNS disease are excluded.
Patients with existing chronic moderate and severe hepatic impairment (Child-Pugh class B or C) are excluded
Patient is concurrently using other approved or investigational antineoplastic agents.
Patient has an active concurrent malignancy requiring active therapy
Trial design
Treatments tested in this trial
- ibrutinib
- Epcoritamab