NCT Number: NCT00073112
A Study of ABT-751 in Patients With Renal Cell Cancer
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.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
B.C. Vancouver Cancer Agency, Vancouver, British Columbia, Canada
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Renal Cell Carcinoma.
- Recurrent tumor.
- At least 6 weeks post-nephrectomy.
- Able to tolerate normal activities of daily living.
- Adequate bone marrow, kidney, and liver function.
Exclusion criteria
- Pregnant or breast feeding.
- Anti-tumor therapy within 4 weeks of the start of ABT-751 administration.
- CNS metastasis.
Treatment and study plan
Primary outcomes
-
Objective Response Rate in subjects with RCC
Time frame: 1 year
Secondary outcomes
-
Time to Tumor Progression (TTP)
Time frame: 1 year
-
Survival
Time frame: 2 years
-
Toxicities associated with treatment administration
Time frame: 1 year
Sponsors and collaborators
Lead sponsor
Abbott
Industry
Registry information
Official study title
A Phase 2 Study of ABT-751 in Subjects With Refractory Colorectal Carcinoma
Important dates
- Study start
- 2003
- Study completion
- 2006
- First posted
- Nov 18, 2003
- Registry last updated
- Nov 29, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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