18
Participants
Start Date
January 31, 2012
Primary Completion Date
May 31, 2014
Study Completion Date
May 31, 2014
TA-650
TA-650 will be intravenously infused at a dosage of 5 mg/kg slowly over a period of more than 2 hours at the first administration (weeks 0), 2, and 6, and then every 8 weeks up to week 46. If the criteria for a dosage escalation are met at the evaluation after week 30, TA-650 will be administered at a dosage of 10 mg/kg after week 30.
Investigational site, Chūbu
Investigational site, Hokkaido
Investigational site, Kanto
Investigational site, Kinki
Investigational site, Kyusyu
Investigational site, Tōhoku
Lead Sponsor
Mitsubishi Tanabe Pharma Corporation
INDUSTRY