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A Study of ABT-751 in Patients With Renal Cell Cancer



A Study of ABT-751 in Patients With Renal Cell Cancer

For Condition: Renal Cell Cancer
Status: Completed
Sponsor(s): Abbott Laboratories ,
Synopsis: The purpose of the study is to determine if ABT-751 will decrease tumors, and determine how long the tumor shrinkage can be maintained in patients with renal cell cancer. Patients will receive ABT-751 by mouth daily for 21 days. Patients will be off drug for 7 days before starting the next cycle of drug.
Details:
Eligibility:
Study Type:
  Interventional, Treatment
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: - Renal Cell Carcinoma. - Recurrent tumor. - At least 6 weeks post-nephrectomy. - Not pregnant or breast feeding. - Able to tolerate normal activites of daily living. - No anti-tumor therapy within 4 weeks of the start of ABT-751 administration. - No CNS metastasis. - Adequate bone marrow, kidney, and liver function.
Total Enrollment: 

Location and Contact Information:

US Oncology IncRaleigh Hematology Oncology Clinic
Cary,  North Carolina,  27511
United States
 

US Oncology IncCancer Care Northwest-North
Spokane,  Washington,  99218
United States
 

US Oncology IncRocky Mountain Cancer Centers
Denver,  Colorado,  80218
United States
 

Oncology Hematology Group of South Florida
Miami,  Florida, 
United States
 

McGill University
Montreal,  Quebec, 
Canada
 

Arizona Cancer Research Center
Tucson,  Arizona,  85712
United States
 

US Oncology IncDayton Oncology & Hematology P.A.
Kettering,  Ohio,  45409
United States
 

Vanderbilt Ingram Cancer Center
Nashville,  Tennessee,  37232-6307
United States
 

US Oncology IncCancer Centers of Florida, P.A.
Orlando,  Florida,  32806
United States
 

US Oncology IncCancer Centers of the Carolinas
Greenville,  South Carolina,  29615
United States
 

West Cancer Clinic
Memphis,  Tennessee,  38120
United States
 

US Oncology IncFlorida Cancer Institute
New Port Richey,  Florida,  34652
United States
 

B.C. Vancouver Cancer Agency
Vancouver,  British Columbia,  V5Z 4E6CAN
Canada
 

UCLA School of Medicine
Los Angeles,  California,  90024
United States
 

Sidney Kimmel Comprehensive Cancer Center
Baltimore,  Maryland,  21231
United States
 

US Oncology IncCancer Care Accociates-Mercy Campus
Oklahoma City,  Oklahoma,  73120
United States
 

US Oncology IncOcala Oncology Center
Ocala,  Florida,  34474
United States
 

US Oncology IncNorthwest Cancer Specialists
Vancouver,  Washington,  98684
United States
 

McMaster University
E., Hamilton,  Ontario,  L8N 4A6
Canada
 

Clinical Trials + Research Associates
Montibello,  California,  90640
United States
 

University of Chicago Medical Center
Chicago,  Illinois,  60637-1471
United States
 

US Oncology IncTyler Cancer Center
Tyler,  Texas,  75702
United States
 

Queen Elizabeth II Health Science Centre
Halifax,  Nova Scotia,  B3H2Y9
Canada
 


Additional Information:
Study ID Numbers:
  M02-416; 
Study Start Date: September 2003
Record last reviewed: May 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00073112

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