Preliminary evaluation of safety and activity of recombinant human interleukin 11 in patients with active Crohn's disease

Background & Aims: Recombinant human interleukin 11 (rhIL-11) is a cytokine with thrombocytopoietic activity and anti-inflammatory and mucosal protect ive effects, The objectives of this study were to investigate the safety an d tolerability of rhIL-11 in patients with Crohn's disease and to explore t he effects of dose and schedule on platelet count and Crohn's disease activ ity. Methods: A multicenter, double-masked, placebo-controlled, dose-escala tion study of 76 patients with active Crohn's disease was performed. Patien ts were randomized to receive subcutaneous placebo or rhIL-11 at doses of 5 , 16, or 40 mu g . kg(-1) . wk(-1) given 2 or 5 times weekly for 3 weeks. C linical and laboratory safety data were recorded, and disease activity was measured at each visit, Results: Subcutaneous injection of rhIL-11 generall y was well tolerated. Significantly greater increases in platelet counts we re found among patients receiving rhIL-11 40 mu g . kg(-1) . wk(-1) as 2 or 5 weekly doses and 16 mu g . kg(-1) . week(-1) as 5 weekly doses compared with patients receiving placebo (P < 0.05), Patients receiving 16 mu g . kg (-1). wk(-1) had the highest clinical response rates, with a response seen in 42% of patients (5/12) receiving 5 weekly doses and 33% of patients (4/1 2) receiving 2 weekly doses, compared with 7% of patients (1/15) receiving placebo. Conclusions: Short-term treatment with rhIL-11 is well tolerated i n patients with active Crohn's disease. The thrombocytopoietic effect of rh IL-11 seems to be both dose and schedule dependent and may be minimized wit h retained clinical benefit in Crohn's disease at 16 mu g . kg(-1) . wk(-1) given in 2 equal doses.