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ABSTRACT: Background
The optimal dose of rituximab in combination with leflunomide in patients with rheumatoid arthritis (RA) is not known.Methods
In Part 1 (previously reported) of the investigator-initiated AMARA study (EudraCT 2009-015950-39; ClinicalTrials.gov NCT01244958), improvements at week (W)24 were observed in patients randomized to rituximab + leflunomide compared with placebo + leflunomide. In the study reported here (Part 2), Part 1 responders received rituximab 500 or 1000 mg at W24/26 plus ongoing leflunomide. Patients were randomized at baseline to their eventual W24 treatment group. The Part 2 primary outcome was the mean Disease Activity Score-28 joints (DAS28) at W52, based on the last observation carried forward (LOCF) analyses and a two-sided analysis of varianc
SUBMITTER: Koehm M
PROVIDER: S-EPMC9784147 | biostudies-literature | 2022 Dec
REPOSITORIES: biostudies-literature