Rheumatoid arthritis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The following individuals who had blood samples stored in the laboratory of Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine with written informed consent: (1) healthy individuals, (2) patients with active rheumatoid arthritis who were untreated at the time of sample collection, (3) patients with rheumatoid arthritis who had achieved clinical remission under tocilizumab at the time of sample collection, and (4) patients with rheumatoid arthritis who had achieved clinical remission under tocilizumab at the time of sample collection and who had discontinued tocilizumab treatment within 12 months of sample collection.
Exclusion criteria
Exclusion criteria: Patients considered unsuitable on medical grounds by study sponsors.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Association between molecular remission status before tocilizumab discontinuation and relapse after discontinuation. | — |
Countries
Japan
Contacts
Keio University School of Medicine Division of Rheumatology, Department of Internal Medicine