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Completed Phase 3 Interventional Results available

Rasburicase Versus Allopurinol in Tumor Patients at Risk for Hyperuricemia and Tumor Lysis Syndrome

ClinicalTrials.gov ID: NCT00230178

Public ClinicalTrials.gov record NCT00230178. 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, 4:52 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

Evaluation of Single Agent Rasburicase for 5 Days Versus Sequential Treatment With Rasburicase From Day 1 Through 3 Followed by Oral Allopurinol From Day 3 Through 5 (Overlap on Day 3) Versus Single Agent Oral Allopurinol for 5 Days in the Management of Plasma Uric Acid in Adult Patients With Leukemia, Lymphoma, and Solid Tumor Malignancies at Risk for Hyperuricemia and Tumor Lysis Syndrome

Study identification

NCT ID
NCT00230178
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
Industry
Enrollment
280 participants

Conditions and interventions

Interventions

  • Rasburicase (SR29142) Drug
  • Allopurinol 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
Mar 31, 2004
Primary completion
Nov 30, 2007
Completion
Nov 30, 2007
Last update posted
Jan 11, 2010

2004 – 2007

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Alta Bates Comprehensive Cancer Center Berkeley California 94704
UCLA Medical Center Los Angeles California 90095
Rocky Mountain Cancer Center Denver Colorado 80218
University of Florida Health Science Center at Jacksonville Jacksonville Florida 32209
Ochsner Clinic Foundation New Orleans Louisiana 70121
Massachusetts General Hospital Boston Massachusetts 02114
New York Methodist Hospital Brooklyn New York 11215
Roswell Park Cancer Institute Buffalo New York 14263
University of Rochester Medical Center Rochester New York 14642
New York Medical College Valhalla New York 10595
Duke University Medical Center Durham North Carolina 27710
Oregon Health and Sciences University Portland Oregon 97201
University of Pennsylvania Health Systems Philadelphia Pennsylvania 19194
University of Texas MD Anderson Cancer Center Houston Texas 77030
Mary Babb Randolph Cancer Center Morgantown West Virginia 26506-9162

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 NCT00230178, 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 Jan 11, 2010 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00230178 live on ClinicalTrials.gov.

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