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Completed Phase 1Phase 2 Interventional Results available

Vorinostat and Combination Chemotherapy With Rituximab in Treating Patients With HIV-Related Diffuse Large B-Cell Non-Hodgkin Lymphoma or Other Aggressive B-Cell Lymphomas

ClinicalTrials.gov ID: NCT01193842

Public ClinicalTrials.gov record NCT01193842. 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 20, 2026, 1:20 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

A Sequential Phase I/Randomized Phase II Trial of Vorinostat and Risk-Adapted Chemotherapy With Rituximab in HIV-Related B-Cell Non-Hodgkin's Lymphoma

Brief summary

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

This partially randomized phase I/II trial studies the side effects and the best dose of vorinostat when given together with combination chemotherapy and rituximab to see how well it works compared to combination chemotherapy alone in treating patients with human immunodeficiency virus-related diffuse large B-cell non-Hodgkin lymphoma or other aggressive B-cell lymphomas. Vorinostat may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Monoclonal antibodies, such as rituximab, may interfere with the ability of cancer cells to grow and spread. Giving vorinostat together with combination chemotherapy and rituximab may kill more cancer cells.

Study identification

NCT ID
NCT01193842
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
107 participants

Conditions and interventions

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 6, 2010 (Actual)
Primary completion
Nov 12, 2016 (Actual)
Completion
May 19, 2022 (Actual)
Last update posted
Nov 21, 2023

2010 – 2022

United States locations

U.S. sites
35
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Jackson Hospital and Clinic Montgomery Alabama 36106 —
UC San Diego Moores Cancer Center La Jolla California 92093 —
UCLA Center for Clinical AIDS Research and Education Los Angeles California 90035 —
UCLA / Jonsson Comprehensive Cancer Center Los Angeles California 90095 —
San Diego VA Medical Center San Diego California 92161 —
Zuckerberg San Francisco General Hospital San Francisco California 94110 —
UCSF Medical Center-Parnassus San Francisco California 94143 —
Jackson Memorial Hospital-Holtz Children's Hospital Miami Florida 33136 —
University of Miami Miller School of Medicine-Sylvester Cancer Center Miami Florida 33136 —
UM Sylvester Comprehensive Cancer Center at Kendall Miami Florida 33176 —
Northwestern University Chicago Illinois 60611 —
John H Stroger Jr Hospital of Cook County Chicago Illinois 60612 —
Stroger Hospital of Cook County MBCCOP Chicago Illinois 60612 —
Louisiana State University Health Science Center New Orleans Louisiana 70112 —
University Medical Center New Orleans New Orleans Louisiana 70112 —
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287 —
Boston Medical Center Boston Massachusetts 02118 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Siteman Cancer Center at Washington University St Louis Missouri 63110 —
Washington University - Jewish St Louis Missouri 63110 —
Washington University School of Medicine St Louis Missouri 63110 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Montefiore Medical Center-Einstein Campus The Bronx New York 10461 —
Montefiore Medical Center-Weiler Hospital The Bronx New York 10461 —
Montefiore Medical Center - Moses Campus The Bronx New York 10467 —
UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27599 —
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210 —
Pennsylvania Hospital Philadelphia Pennsylvania 19107 —
Miriam Hospital Providence Rhode Island 02906 —
Thomas Street Clinic Houston Texas 77009 —
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center Houston Texas 77030 —
Ben Taub General Hospital Houston Texas 77030 —
Virginia Mason Medical Center Seattle Washington 98101 —
Harborview Medical Center Seattle Washington 98104 —
Seattle Cancer Care Alliance Seattle Washington 98109 —

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 NCT01193842, 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 Nov 21, 2023 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01193842 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →