CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 224 enrolled
Drug / intervention
rituximabdrug
Likely dose
rituximab 1000 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01126541
NCT01126541Phase 3Completed

A Comparative Study to Assess the Effect of Retreatment With 2 Doses of MabThera on Disease Activity Score in Patients With Active Rheumatoid Arthritis Who Have Had an Inadequate Response or Intolerance to antiTNF-alfa Therapy.(SMART)

Hoffmann-La Roche·interventional·Posted May 19, 2010·Updated Sep 15, 2014

In Brief

A Phase 3 clinical trial evaluating rituximab for Rheumatoid Arthritis. Completed, enrolled 224 participants across 53 sites.

Detailed Summary

This study will compare the efficacy and safety of re-treatment with 2 doses of MabThera (rituximab) in patients with active rheumatoid arthritis (RA) who have previously experienced an inadequate response or intolerance to anti-tumor necrosis factor (anti-TNF) therapies etanercept, infliximab or adalimumab therapy. All patients will receive infusions of 1000 mg intravenous (IV) MabThera on Days 1 and 15; at Week 24 patients who have demonstrated a moderate or good response will be randomized to receive re-treatment with either 1 or 2 additional infusions of 1000 mg IV MabThera. The anticipated time on study treatment is 2+ years, and the target sample size is 100-500 individuals.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance
Collaborators--

Timeline

Phase 3CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 19, 2010
Enrollment StartSep 1, 2006
Primary CompletionNov 1, 2011
TodayJul 2, 2026
Enrollment to primary: 5.2 yearsPosted 16.1 years ago

Interventions

rituximabdrug

Arm A: 1000 mg IV (one infusion) every 2 months \\nArm B: 2 x 1000 mg IV (2 infusions) every 2 months