Liver Cancer Clinical Trial
Official title:
Phase II Open-Label Study of Sunitinib Malate (SUO11248) in Adult Subjects With Metastatic and/or Surgically Unresectable Hepatocellular Cancers (HCC)
An open label multi-site phase II clinical trial of dose escalated sunitinib malate given orally once daily on days 1-28 of each 42-day cycle. Treatment will be continued until there is either disease progression or cumulative or acute toxicity which in the opinion of the treating physician compromises the ability of the patient to receive treatment or patient desire to stop treatment.
An open label multi-site phase II clinical trial of sunitinib malate given orally once daily
on days 1-28 of each 42-day cycle. Sunitinib malate will be dispensed as capsules at the
beginning of each treatment cycle. The dose may be escalated at the investigator's
discretion. Treatment will be continued until there is either disease progression or
cumulative or acute toxicity which in the opinion of the treating physician compromises the
ability of the patient to receive treatment or patient desire to stop treatment.
A follow up visit will be required before the beginning of every cycle every 6 weeks to
assess toxicity and for physical examination. Complete blood count (CBC) and differential,
comprehensive metabolic panel (including liver function tests) and alpha-feto protein (when
indicated) will be obtained at every scheduled follow up visit.
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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