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Vol 279 No 7478 p555
17 November 2007

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Another anti-TNF tested for ankylosing spondylitis and psoriatic arthritis patients

Tumour necrosis factor inhibitor golimumab — being developed by Centocor and Schering-Plough — has shown promise in phase III studies of psoriatic arthritis and ankylosing spondylitis.

The top-line data were presented at a joint American College of Rheumatology and Association of Rheumatology Health Professionals annual scientific meeting in Boston, Massachusetts, earlier this month.

In one of the studies, 405 patients with active psoriatic arthritis were randomised to receive subcutaneous injections of golimumab (50mg or 100mg) or placebo every four weeks. The primary endpoint — a 20 per cent improvement according to ACR criteria at week 14 — was reached by 50.7 per cent of patients in the 50mg-dose group and by 45.2 per cent of patients in the 100mg-dose group compared with 8.8 per cent of patients on placebo (P<0.001 for both comparisons).

In a second study, 356 ankylosing spondylitis patients were randomised to a similar four-weekly dosing protocol. The researchers found that 59.4 per cent of patients taking 50mg golimumab and 60.0 per cent in the 100mg group saw a 20 per cent improvement in assessment criteria for ankylosing spondylitis at week 14 — the primary endpoint — compared with 21.8 per cent of patients on placebo (P<0.001 for both comparisons).

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