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Completed Phase 3 Interventional Results available

Ofatumumab Versus Rituximab Salvage Chemoimmunotherapy Followed by Autologous Stem Cell Transplant in Relapsed or Refractory Diffuse Large B Cell Lymphoma

ClinicalTrials.gov ID: NCT01014208

Public ClinicalTrials.gov record NCT01014208. 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 17, 2026, 8:22 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

Ofatumumab Versus Rituximab Salvage Chemoimmunotherapy Followed by Autologous Stem Cell Transplant (ASCT) in Relapsed or Refractory Diffuse Large B Cell Lymphoma (DLBCL)

Brief summary

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

This study is being conducted to compare the efficacy and safety of ofatumumab in addition to salvage chemotherapy versus rituximab in addition to salvage chemotherapy in CD20 positive DLBCL subjects relapsing, or with persistent disease, after first-line treatment with rituximab combined with an anthracycline-based chemotherapy regimen and be eligible for ASCT.

Study identification

NCT ID
NCT01014208
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
447 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
Mar 2010 (Type not available)
Primary completion
Feb 2014 (Actual)
Completion
Nov 2014 (Actual)
Last update posted
Aug 7, 2015

2010 – 2014

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
GSK Investigational Site Sacramento California 95816 —
GSK Investigational Site New Haven Connecticut 06520 —
GSK Investigational Site Chicago Illinois 60612-7323 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Westwood Kansas 66205 —
GSK Investigational Site Jackson Mississippi 39216-4505 —
GSK Investigational Site New York New York 10065 —
GSK Investigational Site Syracuse New York 13210 —
GSK Investigational Site Chaple Hill North Carolina 27599-7305 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Providence Rhode Island 02908 —
GSK Investigational Site Charleston South Carolina 29425 —
GSK Investigational Site Greenville South Carolina 29601 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Seattle Washington 98108 —

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 157 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01014208, 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 7, 2015 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01014208 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →