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Completed Phase 2 Interventional Results available

A Phase 2, Multicenter, Randomized, Open-label Study of MEDI-551 in Adults With Relapsed or Refractory Diffuse Large B-Cell Lymphoma (DLBCL)

ClinicalTrials.gov ID: NCT01453205

Public ClinicalTrials.gov record NCT01453205. 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, 7:57 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 2 Randomized Open-label Study of MEDI-551 in Adults With Relapsed or Refractory DLBCL

Brief summary

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

The overall purpose of the study is to determine if MEDI-551, when used in combination with salvage chemotherapy, Ifosfamide-carboplatin-etoposide (ICE) or Dexamethasone-cytarabine (DHAP) in patients with relapsed or refractory DLBCL who are eligible for Autologous Stem Cell Transplant (ASCT), has superior efficacy compared to rituximab in the same population.

Study identification

NCT ID
NCT01453205
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
187 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 99 Years
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 26, 2012
Primary completion
Jul 10, 2016
Completion
Jul 10, 2016
Last update posted
Mar 11, 2018

2012 – 2016

United States locations

U.S. sites
29
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
Research Site Birmingham Alabama 35061
Research Site Burbank California 91501
Research Site Palm Springs California 92262
Research Site Sylmar California 91342
Research Site Atlanta Georgia 30342
Research Site Westwood Kansas 66205
Research Site Hazard Kentucky 41701
Research Site Lafayette Louisiana 70503
Research Site Shreveport Louisiana 71103
Research Site Baltimore Maryland 21215
Research Site Minneapolis Minnesota 55455
Research Site Rochester Minnesota 55905
Research Site Kansas City Missouri 64111
Research Site Kansas City Missouri 66160
Research Site St Louis Missouri 63110
Research Site The Bronx New York 10466
Research Site Fargo North Dakota 58102
Research Site Dayton Ohio 45403
Research Site Newark Ohio 43055
Research Site Sylvania Ohio 43560
Research Site Hershey Pennsylvania 17033
Research Site Philadelphia Pennsylvania 19104
Research Site Charleston South Carolina 29425
Research Site Knoxville Tennessee 37909
Research Site Dallas Texas 75246
Research Site Houston Texas 77030
Research Site Lubbock Texas 79410
Research Site Morgantown West Virginia 26505
Research Site Milwaukee Wisconsin 53266

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 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01453205, 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 Mar 11, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01453205 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →