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Predictions for relapse of rheumatoid arthritis after discontinuation of biologics

Predictions for relapse of rheumatoid arthritis after discontinuation of biologics - Predictions for relapse of rheumatoid arthritis after discontinuation of biologics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000041633
Enrollment
160
Registered
2020-09-01
Start date
2020-09-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid arthritis

Interventions

None listed

Sponsors

Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine.
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime frame
Association between molecular remission status before tocilizumab discontinuation and relapse after discontinuation.

Countries

Japan

Contacts

Public ContactNobuhiko Kajio

Keio University School of Medicine Division of Rheumatology, Department of Internal Medicine

nobuhiko.kajio@keio.jp03-5363-3786

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026