Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Phase 2 Interventional Results available

Treatment Study of Denintuzumab Mafodotin (SGN-CD19A) Plus RICE Versus RICE Alone for Diffuse Large B-Cell Lymphoma

ClinicalTrials.gov ID: NCT02592876

Public ClinicalTrials.gov record NCT02592876. 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 22, 2026, 11:00 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 Randomized, Open-Label Phase 2 Study of Denintuzumab Mafodotin (SGN-CD19A) Plus Rituximab, Ifosfamide, Carboplatin, and Etoposide (19A+RICE) Chemotherapy vs. RICE in the Treatment of Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma (DLBCL) Who Are Candidates for Autologous Stem Cell Transplant

Brief summary

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

The purpose of this randomized, open-label study is to evaluate the safety and efficacy of denintuzumab mafodotin plus RICE (rituximab, ifosfamide, carboplatin, and etoposide) when compared to RICE alone in the treatment of patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) or Grade 3b follicular lymphoma. Eligible patients must also be candidates for autologous stem cell transplant. Patients will be randomly assigned in a 1:1 ratio to receive 3 cycles of study treatment with either denintuzumab mafodotin + RICE or RICE alone. The study will assess whether there is a difference between the 2 groups in the side effects that are reported and the number of patients who achieve complete remission at the end of their study treatment.

Study identification

NCT ID
NCT02592876
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Seagen Inc.
Industry
Enrollment
81 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
Oct 2015 (Actual)
Primary completion
Apr 20, 2018 (Actual)
Completion
Apr 20, 2018 (Actual)
Last update posted
May 17, 2019

2015 – 2018

United States locations

U.S. sites
29
U.S. states
19
U.S. cities
27
Facility City State ZIP Site status
University of Arkansas for Medical Sciences Little Rock Arkansas 72205 —
City of Hope National Medical Center Duarte California 91010-3000 —
Scripps Mercy Cancer Center San Diego California 92103 —
Colorado Blood Cancer Institute Denver Colorado 80218 —
Yale Cancer Center New Haven Connecticut 06520 —
Shands Cancer Center / University of Florida Gainesville Florida 32610 —
University of Miami Miami Florida 33136 —
H. Lee Moffitt Cancer Center & Research Institute Tampa Florida 33612 —
Winship Cancer Institute / Emory University School of Medicine Atlanta Georgia 30322 —
Rush University Medical Center Chicago Illinois 60612 —
University of Chicago Chicago Illinois 60637-1470 —
Cardinal Bernardin Cancer Center / Loyola University Medical Center Maywood Illinois 60153 —
University of Kansas Cancer Center Westwood Kansas United States —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
University of Minnesota Minneapolis Minnesota 55455 —
Washington University School of Medicine St Louis Missouri 63110 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
University of New Mexico Cancer Center Albuquerque New Mexico 87106 —
Memorial Sloan Kettering Cancer Center New York New York 10021 —
UNC Lineberger Comprehensive Cancer Center / University of North Carolina Chapel Hill North Carolina 27599 —
Levine Cancer Institute Charlotte North Carolina 28204 —
Duke University Medical Center Durham North Carolina 27710 —
MD Anderson Cancer Center / University of Texas Houston Texas 77030-4095 —
San Antonio Military Medical Center San Antonio Texas 78234 —
University of Virginia Charlottesville Virginia 22908 —
Seattle Cancer Care Alliance / University of Washington Seattle Washington 98109-1023 —
Carbone Cancer Center / University of Wisconsin Madison Wisconsin United States —
Medical College of Wisconsin (Milwaukee) Milwaukee Wisconsin 53226 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02592876, 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 May 17, 2019 · Synced Oct 22, 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 NCT02592876 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →