Eleven healthy volunteers (six men, five women) and twelve cancer patients (six men, six women) were given single oral doses (2.5 mg/kg body weight) of levarnisole, an immunostimulant agent. In a second experiment eleven healthy et volunteers (six men, five women) and twelve cancer patients (six men, six women) were given single oral doses (5 rug/kg body weight) of levamisole. The levamisole concentrations in plasma (24 h blood sampling) were measured by gas chromatography after extraction. A mono-compartment open model was proposed, and some parameters were calculated. The main results from these two experiments are: the drug was absorbed well, the peak levels of levamisole in the plasma were reached after 1.0 -2.0 hrs and ranged between 0,8 l!g and 1.6 ug/ml with the 2.5 mg and 5 mg/kg body weight doses respectively (concentrations required in vitro to produce an immunological effect); the plasma half-life of levamisole calculated from the decline in the concentration curves varied between 3.3 hand 5.1 h; the absorbed fractions were 0.7 and clearance 310 ml/min; twenty-four hours after medication, the levamisole concentrations in plasma were only 6 % of the peak levels.The interindividual variability in the parameters seemed to be very important; and it may be concluded that the immunostimulant effect critically depends on the dose of the drug. A minimum effective plasma concentration is necessary to trigger its effects, on the other hand high concentrations may produce an immunosuppressive effect.