About the
EPCORE DLBCL-4 Study

The EPCORE DLBCL-4 Study is evaluating the safety and effectiveness of a study drug in combination with an approved anti-lymphoma drug compared to standard-of-care treatment for adults with relapsed or refractory diffuse large B-cell lymphoma (DLBCL).

You may be able to take part in the EPCORE DLBCL-4 Study if you:

If you are interested in participating, the study doctor and staff will review additional eligibility criteria with you.

Study Overview

During the research study, the study drug will be given as a subcutaneous injection (under the skin) in combination with an approved anti-lymphoma drug that will be administered as an oral capsule. The standard-of-care treatment is a combination of 3 drugs that will be given through an intravenous injection (delivered through a tiny tube into the vein).

The study treatment period may last 1–2 years or more, with additional follow-up visits after, depending on your assigned study treatment group and how well the study drug(s) work for you. Total study duration will depend on each participant’s response to their assigned study drugs.

To see if you qualify, please contact:

To see if you qualify,
please contact:
[Site Contact Information]

Consider enrolling
in this study today.

For additional information:
Download the EPCORE DLBCL-4 Study Guide.

This research study is evaluating the safety and effectiveness of an approved drug for a specific investigational use that is currently not approved by regulatory health authorities.

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