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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

16 May 2008

The date of last modification

Mar 03, 2019


Trial Status



Application Summary


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)


Trial Details


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



State of Ethics Review Approval


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 & Sponsor Information


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


Primary study sponsor/organization

A Bour & Company (Ltd)

62, Jethawana Road, Colombo 14.
0114728747
94-11-2342518

Secondary study sponsor (If any)

None





Trial Completion details


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