The purpose of this trial is to determine the effect of raltegravir on pravastatin pharmacokinetics and vice versa by intrasubject comparison.
Inclusion Criteria: * Subject is at least 18 and not older than 55 years of age. * Subject does not smoke more than 10 cigarettes, 2 cigars, or 2 pipes per day. * Subject has a Quetelet Index (Body Mass Index) of 18 to 30 kg/m2. * Subject is able and willing to sign the Informed Consent Form prior to screening evaluations. * Subject is in good age-appropriate health condition. * Subject has a normal blood pressure and pulse rate. Exclusion Criteria: * Documented history of sensitivity/idiosyncrasy to medicinal products or exci-pients. * Positive HIV test. * Positive hepatitis B or C test. * Pregnant female or breast-feeding female. * Therapy with any drug. * Relevant history or presence of pulmonary disorders (especially COPD), car-diovascular disorders, neurological disorders (especially seizures and mi-graine), gastro-intestinal disorders, renal and hepatic disorders, hormonal disorders (especially diabetes mellitus), coagulation disorders. * Fasting triglyceride levels \> 8.0 mmol/L * Relevant history or current condition that might interfere with drug absorption, distribution, metabolism or excretion. * History of or current abuse of drugs, alcohol or solvents. * Inability to understand the nature and extent of the trial and the procedures required. * Participation in a drug trial within 60 days prior to the first dose. * Donation of blood within 60 days prior to the first dose. * Febrile illness within 3 days before the first dose