NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
JRCT ID: jRCT2080221322

Registered date:01/12/2010

Basic Information

Recruitment status
Health condition(s) or Problem(s) studiedRheumatoid Arthritis
Date of first enrollment01/12/2010
Target sample size
Countries of recruitment
Study typeInterventional
Intervention(s)investigational material(s) Generic name etc : T-5224 INN of investigational material : Therapeutic category code : 399 Agents affecting metabolism, n.e.c. Dosage and Administration for Investigational material : Oral administration control material(s) Generic name etc : Placebo INN of investigational material : Therapeutic category code : --- Other Dosage and Administration for Investigational material : Oral administration

Outcome(s)

Primary OutcomeEfficacy and safety
Secondary OutcomeEfficacy and safety

Key inclusion & exclusion criteria

Age minimum>= 20age old
Age maximum<= 64age old
GenderBoth
Include criteria-Male or female. -Subject who have a diagnosis of Rheumatoid Arthritis by the ACR criteria. -Age greater or 20 years and less than 65 years old. -Subject who diagnosed to class 1-3 of Steinblocker dysfunction classification.
Exclude criteria-Subject with autoimmune disease except RA and SS. -Subject who is pregnancy, has possibility of pregnancy, hopes for pregnancy, is suckling.

Related Information

Contact

Public contact
Name
Address https://www.fujifilm.co.jp/form/fftc/en/general/input.php?id=FFTCClinicalEn
Telephone
E-mail
Affiliation FUJIFILM Toyama Chemical Co., Ltd.
Scientific contact
Name
Address
Telephone
E-mail
Affiliation