33
Participants
Start Date
May 22, 2017
Primary Completion Date
July 31, 2021
Study Completion Date
December 31, 2021
Avelumab
"Patients will receive 10 mg/kg of avelumab via intravenous infusion every 2 weeks.~Response evaluation will be performed every 6 weeks (± 1-week window period). Treatment will be continued until disease progression, unacceptable adverse events or the patient's refusal.~Treatment through progression is at the investigator's discretion, and the investigator should ensure that patients do not have any significant, unacceptable, or irreversible toxicity that indicate that continuing treatment will not further benefit the patient. The Investigator should ensure that patients still meet all of the inclusion criteria and none of the exclusion criteria for this study."
Asan Medical Center, Seoul
Lead Sponsor
Merck KGaA, Darmstadt, Germany
INDUSTRY
Asan Medical Center
OTHER