WHO ICTRP trial

Efficacy and safety of rituximab for patients with severe rheumatic disease

JPRN-UMIN000018376 · Japan Primary Registries Network (JPRN) · Not Recruiting

Key facts

Trial ID JPRN-UMIN000018376
Public title Efficacy and safety of rituximab for patients with severe rheumatic disease
Scientific title Efficacy and safety of rituximab for patients with severe rheumatic disease - Efficacy and safety of rituximab for patients with severe rheumatic disease
Primary sponsor Yokohama City University Hospital Department of Pediatrics
Registry Japan Primary Registries Network (JPRN)
Recruitment status Not Recruiting
Study type Interventional
Phase Not selected
Countries Japan
Conditions Childhood-onset severe rheumatic disease (systemic lupus erhythematosus, dermatomyositis, poly myositis, systemic sclerosis , mixed connective tissue disease, Sjogren's syndrome, anti-phospholipid syndrome)
Interventions 1) Induction Therapy rituximab 375mg/m2 (max500mg) 1-4 times/1-2 weeks 2) Maintenance Therapy rituximab 375mg/m2 (max500mg) 1 times/6-12 months
Registration date Jul 22, 2015
Target size 20
Registry page center6.umin.ac.jp

At a glance

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