Why the study?
Does age affect the pharmacokinetics and safety of a single 300-mg oral dose of aliskiren in healthy subjects?
Does age affect the pharmacokinetics and safety of a single 300-mg oral dose of aliskiren in healthy subjects?
Aliskiren exposure is modestly increased in elderly subjects, but its wide therapeutic index suggests no initial dose adjustment is needed for this population.
Higher aliskiren exposure in elderly subjects was associated with age; hypothesis-generating and should not yet change practice.
This open-label, multicenter study compared the pharmacokinetics and safety of the oral direct renin inhibitor aliskiren in 29 elderly (>or=65 years) and 28 young (18-45 years) healthy subjects. Plasma drug concentrations were determined for up to 168 hours following a single 300-mg oral dose of aliskiren. In elderly compared with young subjects, AUC(0-infinity) was 57% higher (ratio of geometric means 1.57, 90% confidence interval: 1.19, 2.06; P = .008) and C(max) was 28% higher (1.28, 90% confidence interval: 0.91, 1.79; P=.233). Other parameters, including t(max) and Vd/F, were similar between age groups. No differences in aliskiren exposure were observed between subjects ages 65 to 74 years (n=16) and >or=75 years (n=13). Aliskiren was well tolerated by all age groups, including the very elderly. In conclusion, aliskiren exposure is modestly increased in elderly subjects. Based on its wide therapeutic index and shallow dose response for blood pressure lowering, no initial dose adjustment should be needed for elderly patients.
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Vaidyanathan et al. (2007) studied this question.
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