The purpose of this study is to determine whether oral ENMD-2076 is effective in treatment of patients with platinum resistant ovarian, fallopian, or peritoneal cancer. Additional sites to be added.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
64
275 mg (or 250 mg for BSA \< 1.65) per day in oral capsules in 28 day continuous cycles
University of Colorado Cancer Center
Aurora, Colorado, United States
University of Chicago Medical Center
Chicago, Illinois, United States
Indiana University Simon Cancer Center
Indianapolis, Indiana, United States
Dana Farber/Partners Cancer Care
Boston, Massachusetts, United States
Progression free survival rate
Time frame: 6 months
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Memorial Sloan-Kettering Cancer Center
New York, New York, United States
Princess Margaret Hospital
Toronto, Ontario, Canada