Inhibition of tumor necrosis factor (TNF)-α action has recently been shown to reverse insulin resistance dramatically and to improve glycemic control in obese rodents. This double-blind study was designed to assess the effects of a recombinant-engineered human TNF-α-neutralizing antibody (CDP571) on glucose homeostasis in obese NIDDM patients. Glycemic control and insulin sensitivity were monitored in 21 NIDDM subjects for a 2-week run-in and then for 6 weeks after treatment in a randomized fashion with a single intravenous dose of either CDP571 (5 mg/kg) or an equivalent volume of normal saline. The prolonged half-life of the antibody ensured adequate plasma levels as measured throughout the study. Concentrations of fasting glucose (CDP571: 10.0 ± 0.8, 10.1 ± 0.8, 10.0 ± 1.0; placebo: 8.5 ± 0.6, 8.1 ± 0.5, 8.7 ± 0.8 mmol/l at baseline, day 1, and week 4, respectively), fasting serum insulin (CDP571:21.2 ± 2.8,21.0 ± 2.8,24.8 ± 3.3; placebo: 19.0 ± 2.8, 20.8 ± 2.9, 17.5 ± 2.2 pmol/l, respectively), and C-peptide remained unaffected by the type of treatment throughout the study. The percentage rate of glucose clearance per minute (KITT) during intravenous insulin sensitivity tests was identical in the CDP571 and placebo groups at baseline and also at 1 and 4 weeks after treatment (mean ± SE; CDP571: 1.33 ± 0.21,1.44 ± 0.25,1.26 ± 0.18; placebo: 1.38 ± 0.15,1.47 ± 0.20, 1.52 ± 0.20;P=0.85, 0.93, and 0.36, respectively). TNF-α neutralization over a period of 4 weeks had no effect on insulin sensitivity in obese NIDDM subjects.Diabetes45:881–885, 1996