Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional Results available

A Phase 3 Study to Assess Efficacy and Safety of Tafasitamab Plus Lenalidomide and Rituximab Compared to Placebo Plus Lenalidomide and Rituximab in Patients With Relapsed/Refractory (R/R) Follicular Lymphoma or Marginal Zone Lymphoma.

ClinicalTrials.gov ID: NCT04680052

Public ClinicalTrials.gov record NCT04680052. 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 Oct 19, 2026, 12:01 AM 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, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Tafasitamab Plus Lenalidomide in Addition to Rituximab Versus Lenalidomide in Addition to Rituximab in Patients With Relapsed/Refractory (R/R) Follicular Lymphoma Grade 1 to 3a or R/R Marginal Zone Lymphoma

Brief summary

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

This is a Phase 3 double-blind, placebo-controlled, randomized study designed to investigate whether tafasitamab and lenalidomide as an add-on to rituximab provides improved clinical benefit compared with lenalidomide as an add-on to rituximab in patients with R/R FL Grade 1 to 3a or R/R MZL.

Study identification

NCT ID
NCT04680052
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Incyte Corporation
Industry
Enrollment
654 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
Apr 15, 2021 (Actual)
Primary completion
Feb 23, 2024 (Actual)
Completion
Aug 9, 2028 (Estimated)
Last update posted
Sep 4, 2026

2021 – 2028

United States locations

U.S. sites
38
U.S. states
21
U.S. cities
36
Facility City State ZIP Site status
John Muir Health Clinical Research Center Concord California 94520-2266 —
Marin Cancer Care Greenbrae California 94904 —
The Oncology Institute of Hope and Innovation Pasadena California 91105 —
Sharp Memorial Hospital San Diego California 92123 —
Middlesex Hospital Cancer Center Middletown Connecticut 06457 —
Smilow Cancer Hospital New Haven Connecticut 06510 —
Cancer Specialists of North Florida Jacksonville Florida 32256 —
Brcr Medical Center, Inc Plantation Florida 33322 —
Asclepes Research Centers Weeki Wachee Florida 34607 —
Northwest Georgia Oncology Centers,P.C Marietta Georgia 30060 —
Straub Medical Center Honolulu Hawaii 96813 —
Des Moines Oncology Research Association Des Moines Iowa 50309 —
Baptist Health Lexington Lexington Kentucky 40503 —
Norton Cancer Institute Louisville Kentucky 40207 —
Tulane University New Orleans Louisiana 70112 —
University of Maryland-Greenebaum Cancer Center Baltimore Maryland 21201 —
Cancer Center For Blood Disorders Bethesda Maryland 20817 —
Barbara Ann Karmanos Cancer Hospital Detroit Michigan 48201 —
Metro-Minnesota Community Oncology Reserch Consortium (Mmcorc) Saint Louis Park Minnesota 55416 —
Hattiesburg Clinic Hematology Hattiesburg Mississippi 39401 —
Roswell Park Cancer Institute Buffalo New York 14263 —
Nyu Clinical Cancer Center New York New York 10016 —
Levine Cancer Institute Charlotte North Carolina 28204 —
Integris Cancer Institute Oklahoma City Oklahoma 73142 —
Charleston Hematology Oncology Associates Charleston South Carolina 29414 —
Prisma Health Upstate Greenville South Carolina 29615 —
Prairie Lakes Health Care System, Inc. Watertown South Dakota 57201 —
Texas Oncology-Baylor Charles A. Sammons Dallas Texas 75246 —
The Center For Cancer and Blood Disorders Fort Worth Texas 76104 —
Lyndon B Johnson General Hospital Houston Texas 77026 —
Md Anderson Cancer Center Houston Texas 77030 —
Renovatio Clinical Spring Texas 77380 —
Utah Cancer Specialists Salt Lake City Utah 84107 —
University of Virginia Medical Center Charlottesville Virginia 22908 —
Vista Oncology Inc Ps Olympia Washington 98506 —
Virginia Mason Medical Center Seattle Washington 98101 —
University of Washington-Seattle Cancer Care Alliance Seattle Washington 98109-4405 —
Northwest Medical Specialties Pllc 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 223 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04680052, 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 Sep 4, 2026 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04680052 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →