NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
JRCT ID: jRCT2080222103

Registered date:10/06/2013

Basic Information

Recruitment status
Health condition(s) or Problem(s) studiedsystemic lupus erythematosus (SLE)
Date of first enrollment10/06/2013
Target sample size
Countries of recruitment
Study typeInterventional
Intervention(s)investigational material(s) Generic name etc : LY2127399 INN of investigational material : Therapeutic category code : 399 Agents affecting metabolism, n.e.c. Dosage and Administration for Investigational material : LY2127399 given as a loading dose of 240 mg at Week 0, followed by 120 mg Q2W or 120 mg Q4W if participant received placebo in BCDS study.LY2127399 given as a loading dose of 120 mg at Week 0, followed by 120 mg Q2W or 120 mg Q4W if participant received LY2127399 in BCDS study.

Outcome(s)

Primary Outcome
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum>= 18age old
Age maximumNot applicable
GenderBoth
Include criteriaHave completed 52 weeks of treatment in BCDS study
Exclude criteria

Related Information

Contact

Public contact
Name
Address 03-3537-5903
Telephone
E-mail
Affiliation Parexel International
Scientific contact
Name
Address
Telephone
E-mail
Affiliation