The University of Chicago
Chicago, Illinois, 60637, United States
NCT Number: NCT00606866
The purpose of this study is to determine maximum tumor shrinkage, time to progression, survival, drug concentration, and degree of skin toxicity.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Chicago, Illinois, 60637, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Placebo for four weeks
Sorafenib 200 mg twice daily
Time frame: 8 weeks
Time frame: 8 weeks
University of Chicago
Other
Dynamic-Contrast Enhanced MRI Pharmacodynamic Study of BAY 43-9006 in Metastatic Renal Cell Carcinoma
Acronym: MRI
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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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