PhaseⅢOpen-label Study of MRA for Rheumatoid Arthritis(RA)

NCT00380601 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2009-12-23

No results posted yet for this study

Summary

An open-label, PhaseⅢ study to evaluate the efficacy and safety of MRA in patients with RA

Conditions

Interventions

DRUG

MRA(Tocilizumab)

8mg/kg/4 weeks

Sponsors & Collaborators

  • Chugai Pharmaceutical

    lead INDUSTRY

Principal Investigators

  • Yuji Kimura · Chugai Pharmaceutical Co., Ltd. Research Dept.1

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-05-31
Primary Completion
2008-08-31
Completion
2009-02-28

Countries

  • Japan

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00380601 on ClinicalTrials.gov