Pharmacokinetics, Safety and Efficacy of BIIL 284 BS in Patients With Rheumatoid Arthritis (RA)

Inclusion Criteria: * Male and female from 18 to 65 years of age * Patients suffering from active rheumatoid arthritis as defined by the ARA criteria revised 1987 \--- At least 4 of the following 7 criteria must have been present: * morning stiffness in and around the joints lasting at least 1 hour before maximal improvement for at least 6 weeks * arthritis (soft tissue thickening or fluid - not bony overgrowth alone) of at least 3 joint areas for at least 6 weeks * arthritis of hand joints (at least one area swollen in a wrist, metacarpophalangeal (MCP) or proximal interphalangeal (PIP) joint) for at least 6 weeks * symmetric arthritis (observed by a physician) with simultaneous involvement of the joints on both sides of the body for at least 6 weeks * rheumatoid nodules (observed by a physician) over bony prominences or extensor surfaces or in juxta-articular regions * serum rheumatoid factor positive * x-ray changes typical of rheumatoid arthritis (erosions or unequivocal bony decalcification localised in or most marked adjacent to the involved joints) * Patient belonging to the RA functional class I, II or III * Patient's written informed consent Exclusion Criteria: * Pregnancy (to be excluded by pregnancy test) or breast feeding * Women of childbearing potential not using adequate contraception * Treatment with methotrexate in the previous month or intended use during the trial period * Treatment with slow acting antirheumatic drugs (SAARDs)/disease-modifying antirheumatic drugs (DMARDs) other than parenteral gold, D-penicillamine, sulfasalazine, chloroquine / hydroxychloroquine corticosteroid during the last 2 months prior to study entry * Treatment with more than one SAARD/DMARD and/or corticosteroid during the last 2 months prior to study entry * Change in treatment with SAARDs/DMARDs during the last 2 months prior to study entry or intended change during the trial duration * Change in treatment with corticosteroids during the last month prior to study entry or intended change during the trial duration * Systemic treatment with corticosteroids at a dose higher than 10 mg/day or 0.2 mg/kg/day (prednisone equivalent), respectively (whichever is lower) during the last month prior to study entry or their intended use during the trial treatment period * Change in treatment with non-steroidal anti-inflammatory drugs (NSAIDs) during the last month prior to study entry or intended change during the trial duration * Treatment with EnbrelTM (etanercept) or experimental therapies during the last 3 months prior to study entry * Synovectomy and/or surgical treatment for RA in the previous month or during the trial * Clinical evidence of known severe cardiovascular, hepatic, renal, respiratory, metabolic, haematological, immunological, gastro-intestinal, hormonal or mental disorders * Any other rheumatological or non-rheumatological disease that could interfere with the evaluation of efficacy and safety * Patients with active malignant disease * Patients with chronic or acute infections during the previous month * Patients with abnormal, clinically relevant laboratory values not related to RA * Participation in another clinical trial during this study or during the previous month * Previous participation in this trial (i.e. having been allocated a randomized treatment number) * Patient unable to comply with the protocol * Patient with known drug abuse * Patient with known alcohol abuse