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Terminated Phase 3 Interventional Results available

Ofatumumab Bendamustine Combination Compared With Bendamustine Monotherapy in Indolent B-cell NHL Unresponsive to Rituxtherapy

ClinicalTrials.gov ID: NCT01077518

Public ClinicalTrials.gov record NCT01077518. 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 Jul 23, 2026, 4:23 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

Randomized Open Label of Ofatumumab and Bendamustine Combination Compared With Bendamustine Monotherapy in Indolent B-cell Non-Hodgkin's Lymphoma Unresponsive to Rituximab or a Rituximab-Containing Regimen During or Within Six Months of Treatment

Study identification

NCT ID
NCT01077518
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
346 participants

Conditions and interventions

Interventions

  • Ofatumumab Drug
  • Bendamustine infusion Drug
  • Ofatumumab and Bendamustine infusions (Arm A) Drug
  • Bendamustine infusion (Arm B) 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
Aug 25, 2010
Primary completion
Jan 2, 2018
Completion
Dec 25, 2018
Last update posted
Mar 26, 2020

2010 – 2018

United States locations

U.S. sites
18
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
Novartis Investigative Site Tucson Arizona 85715
Novartis Investigative Site Beverly Hills California 90211
Novartis Investigative Site Palm Springs California 92262
Novartis Investigative Site Washington D.C. District of Columbia 20037
Novartis Investigative Site Atlanta Georgia 30341
Novartis Investigative Site Coeur d'Alene Idaho 83814
Novartis Investigative Site Silver Spring Maryland 21044
Novartis Investigative Site Detroit Michigan 48202
Novartis Investigative Site St Louis Missouri 63141
Novartis Investigative Site Mineola New York 11501
Novartis Investigative Site Rochester New York 14642
Novartis Investigative Site Danville Pennsylvania 17822
Novartis Investigative Site Philadelphia Pennsylvania 19106
Novartis Investigative Site Charleston South Carolina 29425
Novartis Investigative Site Nashville Tennessee 37203
Novartis Investigative Site Richmond Virginia 23230
Novartis Investigative Site Seattle Washington 98108
Novartis Investigative Site Morgantown West Virginia 26506

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 122 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01077518, 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 26, 2020 · Synced Jul 23, 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 protocol, eligibility criteria, and contact information for NCT01077518 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →