23
Participants
Start Date
July 31, 2011
Primary Completion Date
March 31, 2014
Study Completion Date
March 31, 2014
OPB-31121
Oral administration, 400 mg/day or 600 mg once daily after breakfast during the treatment period (1 month)
OPB-31121 phase2
Oral administration, recommended dose from Phase1 once daily after breakfast during the treatment period (6 months)
Chiba
Tokyo
Lead Sponsor
Otsuka Pharmaceutical Co., Ltd.
INDUSTRY