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Clinical Trial Summary

This study was designed to compare the efficacy and safety of 4.5g iv MP administered in 12 weeks and 4 weeks.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01969019
Study type Interventional
Source Ruijin Hospital
Contact Ning Guang, Professor
Phone (8621)64370045
Email guangning@medmail.com.cn
Status Recruiting
Phase Phase 4
Start date January 2010
Completion date October 2013

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