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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of TA-650 in comparison with a control drug Polyethylene Glycol-treated Human Immunoglobulin (VGIH) in patients with Kawasaki disease refractory to initial therapy with Intravenous Immunoglobulin (IVIG). The pharmacokinetics of TA-650 is also examined.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Kawasaki Disease Refractory to Initial Therapy With Intravenous Immunoglobulin
  • Mucocutaneous Lymph Node Syndrome

NCT number NCT01596335
Study type Interventional
Source Mitsubishi Tanabe Pharma Corporation
Contact
Status Completed
Phase Phase 3
Start date May 2012
Completion date October 2014