JRCT ID: jRCT2080220016
Registered date:02/09/2005
Basic Information
Recruitment status | |
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Health condition(s) or Problem(s) studied | RA |
Date of first enrollment | 02/09/2005 |
Target sample size | |
Countries of recruitment | |
Study type | Interventional |
Intervention(s) | investigational material(s) Generic name etc : MRA (tocilizumab) INN of investigational material : Therapeutic category code : 399 Agents affecting metabolism, n.e.c. Dosage and Administration for Investigational material : Intravenous infusion |
Outcome(s)
Primary Outcome | Efficacy: the ability to inhibit progression of structural damage Safety: Frequency and severity of adverse events and adverse drug reactions |
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Secondary Outcome |
Key inclusion & exclusion criteria
Age minimum | >= 20age old |
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Age maximum | Not applicable |
Gender | |
Include criteria | Inclusion criteria (1) Diagnosed as having RA, on the basis of the criteria stipulated by the American Conference on Rheumatism (ACR) in 1987. (2) At 20 years old |
Exclude criteria |
Related Information
Primary Sponsor | Chugai Pharmaceutical Co., Ltd. |
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Secondary Sponsor | |
Source(s) of Monetary Support | |
Secondary ID(s) | JapicCTI-050016 |
Contact
Public contact | |
Name | |
Address | clinical-trials@chugai-pharm.co.jp |
Telephone | |
Affiliation | Chugai Pharmaceutical Co., Ltd. |
Scientific contact | |
Name | |
Address | |
Telephone | |
Affiliation |