22LL011; Epcoritamab in B-cell Neoplasms

AddtoAny
Share:

WATCH THIS PAGE

Subscribe to be notified of changes or updates to this page.

1 + 13 =
Solve this simple math problem and enter the result. E.g. for 1+3, enter 4.

CHOP in collaboration with AbbVie, is conducting a study for pediatric patients from 1 year of age to 25 years of age with relapsed or refractory aggressive mature B-cell neoplasms (including diffuse large B-cell lymphoma, Burkitt and Burkitt-like lymphoma/leukemia). In this clinical trial, participants will receive the study drug epcoritamab, an immune therapy. Epcoritamab is in clinical development and is being studied for an unapproved use in pediatric patients with B-cell neoplasms. It is not approved for use by the FDA or other global regulatory health authorities. Safety and efficacy are under evaluation. For more information about this study, including specific eligibility criteria, please visit clincialtrials.gov and search for “NCT05206357”. To hear more about this and other available trials or get any questions answered please contact our Cancer Intake Specialist by phone at 267-426-0762 or email oncointake@chop.edu.

Who Do I Contact?

If you are interested in participating in the study or want to learn more please contact our study team at oncointake [at] chop.edu or 267-426-0762.

ClinicalTrials.gov Identifier

Eligibility & Criteria

IRB #:
22-019707
Official Title:
A Single Arm, Open-Label, Phase 1b Trial of Epcoritamab in Pediatric Patients with Relapsed/ Refractory Aggressive Mature B-cell Neoplasms
Study Phase:
Phase I
Eligible Age Range:
1 - 25 Years
Gender:
All
Study Categories:

Visit Criteria

Participants will receive epcoritamab via subcutaneous (under the skin) injections. Study visits will occur at CHOP Main Campus and/or our satellite sites and will include one or more of the following: safety assessments, physical examinations, blood tests, echocardiography, electrocardiography, imaging scans, and other disease assessments. Optional and required tissue collections (left-over or extra) may be collected from biopsies performed as standard of care. Existing tissue samples may also be used in this study.