This study aim was to determine the safety and efficacy of R1507 in combination with letrozole in patients with advanced breast cancer. In the first part of the study a cohort of patients with advanced breast cancer received letrozole 2.5mg po daily in combination with R1507 16mg/kg every 3 weeks.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
6
Unnamed facility
Birmingham, Alabama, United States
Unnamed facility
Washington D.C., District of Columbia, United States
Unnamed facility
Miami, Florida, United States
Unnamed facility
Atlanta, Georgia, United States
Objective Tumor Response (Part 2)
Time frame: Up to 14 months
Pharmacokinetics (PK) Profile (Part 2)
Time frame: Up to 14 months
Progression-free Survival (Part 2)
Time frame: Up to 14 months
Number of Participants With Adverse Events (Part 2)
Time frame: Up to 14 months
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Unnamed facility
St Louis, Missouri, United States
Unnamed facility
Houston, Texas, United States