A Study of Re-Treatment With MabThera (Rituximab) in Patients With Rheumatoid Arthritis Who Have Had an Inadequate Response to a Single Anti-TNF Inhibitor.
- Sponsor
- Hoffmann-La Roche
- Study ID
- NCT00502840
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- rituximab [MabThera/Rituxan] — DRUG1g iv on days 1 and 15
Study Details
This single arm study will evaluate the efficacy and safety of repeated courses of MabThera in patients with active rheumatoid arthritis who have participated in ML19070, and have completed the week 24 visit. Eligible patients (DAS28 \>2.6 after week 24), will receive 2 infusions of 1g MabThera (Day 1 and day 15). For all patients in this extension study, up to 3 repeated courses of treatment are allowed. The anticipated time on study treatment is 1-2 years, and the target sample size is 100-500 individuals.
Key Dates
- Start date
- Jul 23, 2007
- Status verified
- Jul 2017
- Primary completion
- Sep 20, 2011
- Completion
- Sep 20, 2011
Study Design
- Enrollment
- 193 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: 1
Primary Outcome Measure
Change From Baseline in DAS28 Score at Week 24 [ Time Frame: Week 24 ]
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