The purpose of this study is to evaluate fulvestrant in the preliminary stage of breast cancer treatment and assess the relationship between dose, exposure, degree of reduction in tumor markers, and efficacy in postmenopausal women with estrogen receptor positive disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
179
250 mg \& 500 mg intramuscular injection
Research Site
Little Rock, Arkansas, United States
Anti-proliferative effect after 4 weeks of treatment.
Safety, tolerability, tumor response and pharmacokinetics after 4 weeks of treatment.
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Research Site
Boston, Massachusetts, United States
Research Site
Winchester, Massachusetts, United States
Research Site
Albuquerque, New Mexico, United States
Research Site
Hershey, Pennsylvania, United States
Research Site
Nashville, Tennessee, United States
Research Site
Laredo, Texas, United States
Research Site
Innsbruck, Austria
Research Site
Salzburg, Austria
Research Site
Vienna, Austria
...and 21 more locations