An HPLC method for simultaneous determination of LY 195448 (I) and its p-hydroxy metabolite (II) in human blood and urine is presented.The method is based on an Ultrasphere IP 5-μm column, 0.05M heptanesulfonic acid and 0.05M KH2PO4 (pH 3.5) in MeCN-H2O (25:75), as the mobile phase, and a flow-rate of 1 mL/min.Retention times were ≈6, 12, and 15 min for II, internal standard, and I, resp.The extraction efficiency from saline was ≈80%.Standard curves for I in plasma and urine were curvilinear and they were therefore divided into 2 linear segments, 0-1 and 1-20 μg/mL.Concentrations of II in plasma never exceeded 1 μg/mL.The inter-assay coefficients of variation of 4.8 and 3.9% were obtained for I at 0.05 and 5 μg/mL, resp.These data for II were 2.1 and 5.3% at 0.025 and 5.0 μg/mL, resp.The detection limits were 50 and 25 ng/mL for I and II, resp.The pharmacokinetics of I in patients with cancer is described.