Clinical Study of TA-650 in Patients With Behcet's Disease (BD) With Special Lesions

PHASE3CompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

January 31, 2012

Primary Completion Date

May 31, 2014

Study Completion Date

May 31, 2014

Conditions
Behcet's DiseaseBehcet SyndromeNeuro-Behcet's Disease
Interventions
DRUG

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.

Trial Locations (6)

Unknown

Investigational site, Chūbu

Investigational site, Hokkaido

Investigational site, Kanto

Investigational site, Kinki

Investigational site, Kyusyu

Investigational site, Tōhoku

All Listed Sponsors
lead

Mitsubishi Tanabe Pharma Corporation

INDUSTRY