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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 Apr 29, 2026, 12:17 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

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

Study identification

NCT ID
NCT01014208
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
447 participants

Conditions and interventions

Interventions

  • OFATUMUMAB + DHAP Drug
  • RITUXIMAB + DHAP Drug

Drug

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 28, 2010
Primary completion
Jan 31, 2014
Completion
Oct 31, 2014
Last update posted
Aug 6, 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 6, 2015 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01014208 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →