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Efficacy of low dose Rituximab with methotrexate compared to leflunomide with methotrexate in patients with refractory rheumatoid arthritis: A randomized double blind controlled clinical trial
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SLCTR Registration Number
SLCTR/2008/008
Date of Registration
The date of last modification
Mar 03, 2019
Trial Status
Scientific Title of Trial
Efficacy of low dose Rituximab with methotrexate compared to leflunomide with methotrexate in patients with refractory rheumatoid arthritis: A randomized double blind controlled clinical trial
Public Title of Trial
Trial of rituximab in patients with rheumatoid arthritis
Disease or Health Condition(s) Studied
Rheumatoid arthritis refractory to standard disease modifying agents
Scientific Acronym
LORRA
Public Acronym
LORRA
Brief title
None
Universal Trial Number
None
Any other number(s) assigned to the trial and issuing authority
EC/07/029 (Ethics Review Committee of the Faculty of Medicine, University of Colombo)
What is the research question being addressed?
Efficacy and safety of rituximab versus leflunomide in Sri Lankan patients with rheumatoid arthritis ?
Type of study
Interventional
Study design
Allocation
Randomized controlled trial
Masking
Double blinded
Control
Active
Assignment
Other
Purpose
Treatment
Study Phase
Not Available
Intervention(s) planned
Rituximab infusions
Inclusion criteria
1.18-65 years of age 2. must fulfill the revised 1987 American Rheumatism association criteria for at least 6 months 3.Swollen joint count ³4 (28 joint count) and tender joint count ³4(28 joint count at screening and baseline 4.CRP ³6 mg/L OR ESR ³28 mm/h at screening 5. Patients who used methotrexate at 15-25 mg/wk for at least 12 weeks without response. This will include patients who failed to respond to additional treatment with either or both SSZ, chloroquine. patients who have used leflunomide will not be included 6.The doses of MTX must be stable for 4 weeks prior to baseline 7.Prednisolone <10 mg/day or equivalent glucocorticoids are permitted if dose stable for 4 weeks prior to baseline 8.Patients will be allowed to receive non-steroidal anti-inflammatory drugs if dose stable for ³4weeks prior to baseline 9.A negative serum pregnancy test at screening for female subjects of childbearing potential. Use of contraception in patients of reproductive potential
Exclusion criteria
• History of or current inflammatory joint disease other than RA or other systemic rheumatic disorder • Patients with functional class IV according to ACR classification of functional status • Known hypersensitivity to any component of the tetanus toxoid adsorbed vaccine • Evidence of significant uncontrolled concomitant disease, such as diseases of heart, liver, lung, nervous system, renal, endocrine, or gastrointestinal disorders • Known active bacterial, viral, fungal, mycobacterial, or other infection or any major episode of infection requiring hospitalization or treatment with IV antibiotics within 4 weeks of Day 1 or oral antibiotics within 2 weeks of Day 1 • History of serious recurrent or chronic infection history of deep space/tissue infection within 52 weeks prior to baseline. History of or currently active primary or secondary immunodeficiency, including HIV infection • History of cancer, including solid tumors and hematological malignancies • History of alcohol, drug, or chemical abuse within the 6 months prior to screening • Diagnosis of juvenile idiopathic arthritis/juvenile rheumatoid arthritis before age 16 • Immunization with a live vaccine within 4 weeks prior to randomization (Day 1) • Serum creatinine > 1.4 mg/dl for women or > 1.6 mg/dl for men • AST or ALT > 2.5 times upper limit of normal • Platelet count < 100,000/ml • Hemoglobin < 8.0 g/dl • Neutrophils < 1.5x10^3/ml • Positive tests for hepatitis B surface antigen • Levels of IgG < 5.0 mg/ml and/or IgM = 0.4 mg/ml
Primary outcome(s)
1.
(ACR) 20% improvement of response(ACR 20) at 24 weeks |
[ 6 months, 1 year and two years after the first infusion of drug ] |
2.
Disease activity score 28 (DAS 28) improvement at 24 weeks |
[ 6 months, 1 year and two years after the first infusion of drug ] |
Secondary outcome(s)
1.
ACR50 and ACR70 improvement atweek 24, 1 year and 2 years |
[ 6 months, 1 year and two years after the first infusion of drug ] |
2.
Immunological markers which include rheumatoid factor, B cells (CD 19) and T-cell (CD3,CD27) and immunoglobulin levels (IgG,IgM,IgA) |
[ 6 months, 1 year and two years after the first infusion of drug ] |
3.
Side effects noted with rituximab and leflunomide, particularly the rate of infections |
[ 6 months, 1 year and two years after the first infusion of drug ] |
4.
The antibody response to tetanus toxoid and pneumococcal vaccine given at 36 weeks |
[ 6 months, 1 year and two years after the first infusion of drug ] |
Target number/sample size
40
Countries of recruitment
Sri Lanka
Anticipated start date
2008-01-20
Anticipated end date
2010-01-20
Date of first enrollment
Date of study completion
Recruitment status
Recruiting
Funding source
Test kits, Rituximab vials and Research Assistant will be provided by Roche Pharmaceuticals.
Regulatory approvals
Status
Approved
Date of Approval
2007-05-17
Approval number
EC/07/029
Details of Ethics Review Committee
Name: | Ethics Review Committee, Faculty of Medicine, University of Colombo |
Institutional Address: | No. 25, Kynsey Road, Colombo 00800 Sri Lanka |
Telephone: | +94-11-2695300 (Extension: 240) |
Email: | ethicscommitteemfc@gmail.com |
Contact person for Scientific Queries/Principal Investigator
Dr. Lalith S. Wijayaratne MBBS, MD, MRCP
Consultant Rheumatologist,
Department of Rheumatology and Rehabilitation,
The National Hospital of Sri Lanka.
0777300414
Contact Person for Public Queries
Dr. Harindu Wijesinghe
Senior Registrar in Rheumatology,
Department of Rheumatology and Rehabilitation,
The National Hospital of Sri Lanka.
0777749666
drharindu@yahoo.com
Do the investigators plan to share identified individual clinical trial participant-level data (IPD)?
IPD sharing plan description
Not Available
Study protocol available
Protocol version and date
Not Available
Protocol URL
Not Available
Results summary available
No
Date of posting results
Date of study completion
Final sample size
Date of first publication
Link to results
Brief summary of results