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Clinical Trials/NL-OMON23732
NL-OMON23732
Completed
Not Applicable

The REDO study: RhEumatoid arthritis REtreatment with ultra-low dose Rituximab: Disease Outcome after Dose Optimization

The Sint Maartenskliniek0 sites140 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rheumatoid Arthritis
Sponsor
The Sint Maartenskliniek
Enrollment
140
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
The Sint Maartenskliniek

Eligibility Criteria

Inclusion Criteria

  • Rheumatoid arthritis: either 2010 ACR RA and/or 1987 RA criteria and/or clinical diagnosis of the treating rheumatologist, fulfilled at any time point between start of the disease and inclusion.
  • RTX retreatment: at least once RTX in the last 18 months for RA in a dose of 1 × 1000 mg, 2 × 1000 mg or 2 × 500 mg and no other biologicals received after last RTX dose. Patients treated with innovator RTX (MabThera) as well as registered biosimilars will be included.

Exclusion Criteria

  • Patients with known (non\-)response to ultra\-low dose RTX (below 1 × 1000 mg)
  • Current corticosteroid dosing above 10 mg per day prednisolone equivalent

Outcomes

Primary Outcomes

Not specified

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