drugset / Trial / NCT04663347

Safety and Efficacy Trial of Epcoritamab Combinations in Subjects With B-cell Non-Hodgkin Lymphoma (B-NHL)

NCT04663347

Phase 1/2 Active not recruiting 543 enrolled Genmab AbbVie · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this trial is to measure the safety and effectiveness of epcoritamab (EPKINLY™), either by itself or together with other therapies, when treating participants with B-cell non-Hodgkin Lymphoma (B-NHL). The aim of the first part of the trial is to identify the most appropriate dose of epcoritamab, and the aim of the second part of the trial is to assess the selected epcoritamab dose in a larger group of participants with B-NHL. All participants in this trial will receive either epcoritamab alone, or epcoritamab combined with another standard treatment regimen, with a total of 10 different treatment arms being studied. Trial details include: * The treatment duration for each participant depends upon which arm of treatment they are assigned to. * The visit frequency for each participant depends upon which arm of treatment they are assigned to, but will be weekly to start for all participants, then will decrease to either: every 2 weeks, or every 3 weeks, or every 4 weeks, or every 8 weeks. * All participants will receive active drug; no one will be given placebo. Participants who receive treatment with epcoritamab will have it injected right under the skin. Participants will receive a different regimen of epcoritamab depending upon which arm of treatment they are assigned. Participants who receive standard treatments will have intravenous (IV) infusions and/or oral administration of those treatments. Participants will receive a different standard treatment regimen depending upon which arm of treatment they are assigned.

Timeline

Start
2020-11-03
Primary completion
2027-09-30
Completion
2027-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Epcoritamab Monoclonal antibody 48 mg Subcutaneous
Background Bendamustine Small molecule
Background Carboplatin Small molecule
Background Cyclophosphamide Other / unclassified
Background Cytarabine Small molecule
Background Dexamethasone Small molecule
Background Doxorubicin Other / unclassified
Background Etoposide Small molecule
Background Gemcitabine Small molecule
Background Ifosfamide Small molecule
Background Lenalidomide Other / unclassified 20 mg Oral
Background Oxaliplatin Small molecule
Background Prednisone Other / unclassified
Background Rituximab Monoclonal antibody 375 mg/m2
Background Vincristine Small molecule