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Completed Phase 2 Interventional Results available

Trial of Bendamustine, Bortezomib, and Rituximab in Patients With Previously Untreated Low Grade Lymphoma

ClinicalTrials.gov ID: NCT01029730

Public ClinicalTrials.gov record NCT01029730. 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 26, 2026, 12:40 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

Phase II Trial of Bendamustine, Bortezomib, and Rituximab in Patients With Previously Untreated Low Grade Lymphoma

Brief summary

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

The goal of this multi-center Phase II study is to add bortezomib to the highly active regimen of bendamustine and rituximab. In this study, bortezomib will be administered on a weekly schedule (Days 1, 8, 15) and will be added to bendamustine/rituximab given in 4-week cycles. This combination uses the standard bendamustine dosing schedule, and is more convenient than the 5-week regimen of these 3 drugs currently being studied.

Study identification

NCT ID
NCT01029730
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
55 participants

Conditions and interventions

Conditions

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
Mar 2010 (Type not available)
Primary completion
Oct 2014 (Actual)
Completion
Jul 2016 (Actual)
Last update posted
Aug 19, 2016

2010 – 2016

United States locations

U.S. sites
20
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
NEA Baptist Clinic Jonesboro Arkansas 72401 —
Holy Cross Hospital Fort Lauderdale Florida 33308 —
Florida Cancer Specialists Fort Myers Florida 33916 —
Northeast Georgia Medical Center Gainesville Georgia 30501 —
Hematology Oncology of the North Shore Skokie Illinois 60076 —
Providence Medical Group Terre Haute Indiana 47802 —
Baptist Hospital East Louisville Kentucky 40207 —
Hematology Oncology Clinic, LLP Baton Rouge Louisiana 70806 —
Center for Cancer and Blood Disorders Bethesda Maryland 20817 —
National Capital Clinical Research Consortium Bethesda Maryland 20817 —
Grand Rapids Clinical Oncology Program Grand Rapids Michigan 49503 —
St. Louis Cancer Care Chesterfield Missouri 63017 —
Portsmouth Regional Hospital Portsmouth New Hampshire 03801 —
Hematology-Oncology Associates of Northern NJ Morristown New Jersey 07960 —
Oncology Hematology Care Cincinnati Ohio 45242 —
Cancer Centers of Southwest Oklahoma Lawton Oklahoma 73505 —
Chattanooga Oncology Hematology Associates Chattanooga Tennessee 37404 —
Tennessee Oncology, PLLC Nashville Tennessee 37023 —
The Center for Cancer and Blood Disorders Fort Worth Texas 76104 —
Schiffler Cancer Center Wheeling West Virginia 26003 —

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 NCT01029730, 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 19, 2016 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01029730 live on ClinicalTrials.gov.

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