A Study of Epcoritamab and Ibrutinib in People With Central Nervous System Lymphoma (CNSL)

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

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

Treatment groups

26 Participants
are divided into 3 treatment groups