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Active, not recruiting Phase 3 Interventional

Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Previously Untreated Follicular Lymphoma

ClinicalTrials.gov ID: NCT06191744

Public ClinicalTrials.gov record NCT06191744. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 3:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multicenter, Randomized, Open-Label Trial to Evaluate the Safety and Efficacy of Epcoritamab + Rituximab and Lenalidomide (R2) Compared to Chemoimmunotherapy in Previously Untreated Follicular Lymphoma (EPCORE™FL-2)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Follicular lymphoma (FL) is the second most common B-cell cancer and the most common type of cancer of lymphocytes. Unfortunately, this disease is incurable with conventional treatment and the disease recurs in almost all patients. This study will assess how safe and effective epcoritamab is in combination with lenalidomide and rituximab (R2) in treating adult participants with previously untreated FL. Adverse events and change in disease condition will be assessed. Epcoritamab is an investigational drug being developed for the treatment of FL. Study doctors put the participants in 1 of 5 groups, called treatment arms. Each group receives a different treatment. Around 1095 adult participants with previously untreated FL will be enrolled in approximately 250 sites across the world. Participants will receive R2 (intravenous \[IV\] infusion of rituximab (R) and oral capsules of lenalidomide) alone or in combination with subcutaneous injections of epcoritamab. Participants may also receive investigator's choice chemoimmunotherapy (CIT): IV infusion of obinutuzumab (G) and IV injections of cyclophosphamide, IV injections of doxorubicin, IV injections of vincristine, oral tablets of prednisone (CHOP) \[G-CHOP\]/ R-CHOP or G and IV infusion of bendamustine (Benda) \[G-Benda\]/R-Benda. The total treatment duration will be 120 weeks for all arms except A2, which is 24 weeks of treatment. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.

Study identification

NCT ID
NCT06191744
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Genmab
Industry
Enrollment
1,095 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 4, 2024
Primary completion
Oct 31, 2037
Completion
Oct 31, 2037
Last update posted
Aug 3, 2026

2024 – 2037

United States locations

U.S. sites
58
U.S. states
25
U.S. cities
51
Facility City State ZIP Site status
UCSF Fresno /ID# 264712 Fresno California 93701-2302
Scripps Mercy Hospital /ID# 265393 San Diego California 92103
Sansum Clinic Research /ID# 261596 Santa Barbara California 93105
Rocky Mountain Cancer Centers - Boulder /ID# 261203 Boulder Colorado 80303
Christiana Care Health Service /ID# 261207 Newark Delaware 19713
Cancer Specialists of North Florida - Jacksonville - AC Skinner Parkway /ID# 262445 Jacksonville Florida 32256
Advent Health /ID# 261578 Orlando Florida 32803
Orlando Health Cancer Institute /ID# 260983 Orlando Florida 32806
Moffitt Cancer Center /ID# 259487 Tampa Florida 33612-9416
Beacon Cancer Care - Coeur d'Alene /ID# 260670 Coeur d'Alene Idaho 83814
Northwestern Medicine - Northwestern Memorial Hospital /ID# 259814 Chicago Illinois 60611
Cancer Care Specialists Of Central Illinois /ID# 272464 Decatur Illinois 62526
Loyola University /ID# 259462 Maywood Illinois 60153
Illinois Cancer Care, PC /ID# 261526 Peoria Illinois 61615
Fort Wayne Medical Oncology and Hematology- South Office /ID# 259583 Fort Wayne Indiana 46804
University of Iowa Health Care /ID# 262132 Des Moines Iowa 50314-3017
University of Louisville Hospital /ID# 260544 Louisville Kentucky 40202
Norton Cancer Institute - St. Matthews /ID# 261076 Louisville Kentucky 40207
New England Cancer Specialists - Westbrook /ID# 260672 Westbrook Maine 04092
University of Maryland, Baltimore /ID# 259538 Baltimore Maryland 21201
Center for Cancer and Blood Disorders-American Oncology Partners of Maryland /ID# 259476 Bethesda Maryland 20817
St. Luke's Hospital - Chesterfield /ID# 260489 Chesterfield Missouri 63017
Intermountain Health St Vincent Regional Hospital - Cancer Centers of Montana /ID# 260006 Billings Montana 59102
Nebraska Cancer Specialists (NCS) - Regional Cancer Center - St Francis Location /ID# 262506 Grand Island Nebraska 68803
Nebraska Hematology-Oncology /ID# 269692 Lincoln Nebraska 68506
Nebraska Cancer Specialists - Omaha - Wright Street /ID# 262505 Omaha Nebraska 68130
University of Nebraska Medical Center /ID# 261996 Omaha Nebraska 68198
University of New Mexico /ID# 261083 Albuquerque New Mexico 87102-4517
Presbyterian Kaseman Hospital /ID# 262451 Albuquerque New Mexico 87110
Presbyterian Rust Medical Center /ID# 262447 Rio Rancho New Mexico 87124
New York Oncology Hematology - Albany Cancer Center /ID# 261814 Albany New York 12206-5013
NYU Langone Hospital - Long Island /ID# 265531 Mineola New York 11501
NYU Langone Medical Center /ID# 264518 New York New York 10016-6402
Icahn School of Medicine at Mount Sinai /ID# 259595 New York New York 10029
New York Oncology Hematology /ID# 270208 Troy New York 12180
Clinical Research Alliance - Westbury /ID# 261078 Westbury New York 11590
Novant Health Presbyterian Medical Center /ID# 259740 Charlotte North Carolina 28204
Novant Health Forsyth Medical Center /ID# 259741 Winston-Salem North Carolina 27103
Oncology Hematology Care, Inc - Blue Ash /ID# 261204 Cincinnati Ohio 45252
Taylor Cancer Research Center /ID# 260488 Maumee Ohio 43537-1921
Oncology Associates of Oregon, P.C. /ID# 261816 Eugene Oregon 97401
MUSC Hollings Cancer Center /ID# 259604 Charleston South Carolina 29425
Prisma Health /ID# 259602 Greenville South Carolina 29605
Sarah Cannon Research Institute - Tristar Centennial Medical Center /ID# 274985 Nashville Tennessee 37203
Texas Oncology - Austin Midtown /ID# 261208 Austin Texas 78705
Texas Oncology- Baylor Charles A. Sammons Cancer Center /ID# 261206 Dallas Texas 75246-2003
MD Anderson Cancer Center /ID# 260984 Houston Texas 77030-4000
Oncology Consultants /ID# 268390 Houston Texas 77030
Joe Arrington Cancer Research /ID# 260382 Lubbock Texas 79410
Intermountain Healthcare LDS Hospital /ID# 259759 Salt Lake City Utah 84143
Virginia Cancer Specialists - Fairfax /ID# 261205 Fairfax Virginia 22031
Oncology and Hematology Associates of Southwest Virginia /ID# 261592 Roanoke Virginia 98684
Swedish Cancer Institute - Edmonds /ID# 266356 Edmonds Washington 98026
Swedish Cancer Institute - Issaquah /ID# 266358 Issaquah Washington 98029
Vista Oncology - East Olympia /ID# 261360 Olympia Washington 98506-5028
Virginia Mason Hospital and Medical Center /ID# 260549 Seattle Washington 98101
Swedish Medical Center - Seattle /ID# 260370 Seattle Washington 98104
Northwest Medical Specialties - Tacoma /ID# 262133 Tacoma Washington 98405

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 208 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06191744, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 3, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06191744 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →