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Completed Phase 2 Interventional

Bendamustine Combined With Rituximab for Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma

ClinicalTrials.gov ID: NCT00831597

Public ClinicalTrials.gov record NCT00831597. 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 7, 2026, 3:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

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

A phase II trial to evaluate the efficacy and safety of combination bendamustine and rituximab in patients with relapsed or refractory diffuse large B-cell lymphoma. It is hypothesized that the BR combination will produce at least a 70% overall response rate.

Study identification

NCT ID
NCT00831597
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pharmatech
Industry
Enrollment
61 participants

Conditions and interventions

Interventions

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
Oct 31, 2008
Primary completion
Jul 31, 2013
Completion
Aug 31, 2013
Last update posted
Apr 18, 2016

2008 – 2013

United States locations

U.S. sites
33
U.S. states
17
U.S. cities
32
Facility City State ZIP Site status
Pharmatech Oncology Study Site Beverly Hills California 90211
Pharmatech Oncology Study Site Fountain Valley California 92708
Pharmatech Oncology Study Site Oxnard California 93030
Pharmatech Oncology Study Site Washington D.C. District of Columbia 20037
Pharmatech Oncology Study Site Washington D.C. District of Columbia 20422
Pharmatech Oncology Study Site Boynton Beach Florida 33435
Pharmatech Oncology Study Site Brooksville Florida 34613
Pharmatech Oncology Study Site Gainesville Florida 32605
Pharmatech Oncology Study Site Titusville Florida 32796
Pharmatech Oncology Study Site Joliet Illinois 60435
Pharmatech Oncology Study Site Lafayette Indiana 47904
Pharmatech Oncology Study Site Muncie Indiana 47303
Pharmatech Oncology Study Site Dubuque Iowa 52001
Pharmatech Oncology Study Site Paducah Kentucky 42001
Pharmatech Oncology Study Site York Village Maine 03909
Pharmatech Oncology Study Site Jackson Mississippi 39202
Pharmatech Oncology Study Site Chesterfield Missouri 63017
Pharmatech Oncology Study Site Cherry Hill New Jersey 08003
Pharmatech Oncology Study Site Phillipsburg New Jersey 08865
Pharmatech Oncology Study Site Bay Shore New York 11706
Pharmatech Oncology Study Site East Setauket New York 11733
Pharmatech Oncology Study Site The Bronx New York 10467
Pharmatech Oncology Study Site Akron Ohio 44304
Pharmatech Oncology Study Site Columbus Ohio 43219
Pharmatech Oncology Study Site Bethlehem Pennsylvania 18015
Pharmatech Oncology Study Site Gettysburg Pennsylvania 17325
Pharmatech Oncology Study Site Hilton Head South Carolina 29926
Pharmatech Oncology Study Site Germantown Tennessee 38138
Pharmatech Oncology Study Site Austin Texas 78759
Pharmatech Oncology Study Site Corpus Christi Texas 78463
Pharmatech Oncology Study Site Fort Worth Texas 76104
Pharmatech Oncology Study Site Lubbock Texas 79410
Pharmatech Oncology Study Site Richardson Texas 75080

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 NCT00831597, 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 Apr 18, 2016 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00831597 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →