About the EPCORE FL-2 Study

The EPCORE FL-2 Study is evaluating the safety and effectiveness of an investigational drug in combination with a chemotherapy-free regimen compared to standard-of-care chemoimmunotherapy for adults with newly diagnosed follicular lymphoma.

You may be able to take part in the EPCORE FL-2 Study if you:

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

Study Overview

The investigational drug will be given as a subcutaneous injection (under the skin). One standard-of-care drug will be given through an intravenous injection (delivered through a tiny tube into the vein) and another standard-of-care drug is a capsule or tablet that will be taken by mouth. Some participants will be given the study doctor’s choice of standard-of-care chemoimmunotherapy; the drugs in these regimens are administered as intravenous infusions or injections, with the exception of prednisone, which is taken by mouth.

The study treatment period is approximately 2.5 years, with additional follow-up visits after. The total study duration will depend on each participant’s response to the study drugs.

For additional information: Download the EPCORE FL-2 Study Guide.

Consider enrolling in this study today.

This investigational drug being studied in patients with follicular lymphoma is under clinical development and is not approved for use by regulatory health authorities. Safety and effectiveness are under evaluation.

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