18
Participants
Start Date
January 24, 2012
Primary Completion Date
December 22, 2016
Study Completion Date
December 22, 2016
OCV-501
"1. Before the recommended dose will be decided OCV-501 will be subcutaneously administered once a week at the dose in the study 311-10-001.~2. After the recommended dose will be decided OCV-501 will be subcutaneously administered once a week at the recommended dose."
National Cancer Center, Tokyo
Lead Sponsor
Otsuka Pharmaceutical Co., Ltd.
INDUSTRY