To determine the antitumor efficacy and the safety of SU-014813 at a dose of 100 mg orally once daily in patients with Metastatic Breast Cancer
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
90
100 mg capsule/day for 6 cycle of 21 days
Pfizer Investigational Site
Los Angeles, California, United States
To determine the antitumor efficacy of single agent SU-014813 at a dose of 100 mg orally once daily in patients with MBC
Time frame: June 2008
To assess onset and duration of tumor control and 1-year survival rate
Time frame: AUG 2008
To evaluate the safety of SU-014813To assess patient reported outcomes
Time frame: AUG 2008
To determine SU-014813 plasma trough concentration (Ctrough)
Time frame: AUG 2008
To explore the relationship between Ctrough and efficacy, safety, and biomarkers
Time frame: AUG 2008
To explore the correlations of cancer biomarkers with treatment-related outcomes
Time frame: AUG 2008
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Pfizer Investigational Site
Pasadena, California, United States
Pfizer Investigational Site
Santa Monica, California, United States
Pfizer Investigational Site
Valancia, California, United States
Pfizer Investigational Site
Corinth, Mississippi, United States
Pfizer Investigational Site
Southaven, Mississippi, United States
Pfizer Investigational Site
Memphis, Tennessee, United States
Pfizer Investigational Site
Memphis, Tennessee, United States
Pfizer Investigational Site
Hamburg, Germany
Pfizer Investigational Site
Magdeburg, Germany
...and 12 more locations