About the
EPCORE NHL-5 Study

The EPCORE NHL-5 Study is evaluating the safety and tolerability of a primary investigational drug in combination with other drugs for adults with non-Hodgkin lymphoma (NHL). The study is meant for those with specific types of treatment-naïve, relapsed, or refractory NHL. 

  • Treatment-naïve: You have not had any treatments for this type of cancer 
  • Relapsed: Your cancer previously responded to therapy but progressed 6 months or later after completing therapy
  • Refractory: Your cancer either progressed during therapy, did not respond to prior therapy, or progressed within 6 months after completing therapy (including maintenance therapy)

You may be able to take part in the EPCORE NHL-5 Study if you:

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

Study Overview

Different investigational combinations of drugs will be tested in this study and the study doctor will choose the combination that is right for you. These combinations of drugs are investigational because they have not been approved to treat these diseases by the regulatory authority in your country. There is no placebo in this study, which means all participants will receive study treatment.

There are multiple study treatment groups, or arms, for this study. You will be assigned to a group depending on your disease.

The primary investigational drug will be given as a subcutaneous injection (under the skin). The other drugs will either be given through an intravenous infusion (delivered through a tiny tube into the vein) or as a capsule or tablet that will be taken by mouth.

The study treatment period may last from 24 weeks to 2 years or more depending on your study treatment arm and how well the study drug(s) work for you. Total study duration will depend on each participant’s response to the study drug(s).

For additional information: Download the EPCORE NHL-5 Study Guide.

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

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