Objective To investigate the 2-year clinical and radiological outcomes of patients with early rheumatoid arthritis (RA; symptom duration <1 year) who had initially responded well to methotrexate monotherapy.
Johnson & Johnson's Janssen Biotech unit announced Friday the receipt of a complete response letter from US regulators regarding the company's filing for expanded approval of Simponi (golimumab) for limiting the progression of structural damage in patients with moderately to severely active rheumatoid arthritis.
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