26
Participants
Start Date
February 20, 2018
Primary Completion Date
September 28, 2023
Study Completion Date
September 28, 2023
Pembrolizumab
All subjects will receive pembrolizumab 200mg IV every 3 weeks until disease progression or unacceptable toxicity.
Chemotherapy
At time of progression, all subjects will also have the option of receiving taxane-based chemotherapy followed by repeat pembrolizumab for those who have a clinical response to chemotherapy. Chemotherapy regimen will be at the discretion of the treating physician, and may consist of docetaxel or cabazitaxel with or without a platinum agent (e.g. carboplatin). A minimum of 4 cycles and a maximum of 8 cycles of chemotherapy will be given.
University of California, San Francisco, San Francisco
Merck Sharp & Dohme LLC
INDUSTRY
National Cancer Institute (NCI)
NIH
University of California, San Francisco
OTHER