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Completed Phase 1 Interventional

Bortezomib, Ifosfamide, Carboplatin, and Etoposide, With or Without Rituximab, in Treating Patients With Relapsed or Refractory AIDS-Related Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT00598169

Public ClinicalTrials.gov record NCT00598169. 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 6, 2026, 7:28 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

Safety and Efficacy Pilot Trial of the Anti-Viral and Anti-Tumor Activity of Velcade Combined With (R)ICE in Subjects With EBV and/or HHV-8 Positive Relapsed/Refractory AIDS-Associated Non-Hodgkin's Lymphoma

Brief summary

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

RATIONALE: Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the cancer. Drugs used in chemotherapy, such as dexamethasone, ifosfamide, carboplatin, and etoposide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. It is not yet known whether giving bortezomib together with combination chemotherapy is more effective with or without rituximab in treating AIDS-related non-Hodgkin lymphoma. PURPOSE: This clinical trial is studying giving bortezomib together with dexamethasone, ifosfamide, carboplatin, and etoposide to see how well it works with or without rituximab in treating patients with relapsed or refractory AIDS-related non-Hodgkin lymphoma.

Study identification

NCT ID
NCT00598169
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
AIDS Malignancy Consortium
Network
Enrollment
23 participants

Conditions and interventions

Conditions

Interventions

Biological · Drug · Genetic

Eligibility (public fields only)

Age range
18 Years to 120 Years
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, 2007
Primary completion
Sep 30, 2014
Completion
Oct 31, 2014
Last update posted
Aug 9, 2020

2007 – 2014

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Rebecca and John Moores UCSD Cancer Center La Jolla California 92093-0658
USC/Norris Comprehensive Cancer Center and Hospital Los Angeles California 90089-9181
UCLA Clinical AIDS Research and Education (CARE) Center Los Angeles California 90095-1793
University of California at Davis Center for Aids Research and Education Services Sacramento California 95814
University of Miami Sylvester Comprehensive Cancer Center - Miami Miami Florida 33136
Emory Winship Cancer Institute Atlanta Georgia 30322
Cancer Research Center of Hawaii Honolulu Hawaii 96813
Northwestern Cancer Center Chicago Illinois 60611
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21231-2410
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Memorial Sloan-Kettering Cancer Center New York New York 10065
Montefiore Medical Center The Bronx New York 10467-2490
Arthur G. James Cancer Hospital and Richard J. Solove Research Institute at Ohio State University Comprehensive Cancer Center Columbus Ohio 43210-1240
Pennsylvania Oncology Hematology Associates, Incorporated - Philadelphia Philadelphia Pennsylvania 19106
Thomas Street Health Center Houston Texas 77009
Baylor College of Medicine Houston Texas 77030-2707
Virginia Mason Medical Center Seattle Washington 98101

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 NCT00598169, 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 9, 2020 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00598169 live on ClinicalTrials.gov.

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