Abstract
A bioequivalence study of 2 irbesartan (CAS 138402-11-6) film-coated tablet formulations
was carried out in 40 healthy volunteers according to an open label, randomized, 2-period,
2-sequence, crossover, single dose and fasting conditions design. The test and reference
formulations were administered in 2 treatment days, separated by a washout period
of 7 days. Blood samples were drawn up to 96 h following drug administration. Plasma
concentrations of irbesartan were obtained by a validated HPLC method using MS/MS
detection. Log-transformed AUC0–t and Cmax values were tested for bioequivalence based on the ratios of the geometric LSmeans
(test/reference). tmax was analysed nonparametrically. The 90% confidence intervals of the geometric LSmean
values for the test/reference ratios for AUC0–t (98.06–109.48%, point estimator 103.61%) and Cmax (88.93–100.87%, point estimator 94.72%) were within the bioequivalence acceptance
range of 80–125%. According to the European Guideline on the Investigation of Bioequivalence
it may be therefore concluded that test formulation of irbesartan 300 mg film-coated
tablet is bioequivalent to the reference formulation. Overall, it was judged that
the study was conducted with a good tolerance of the subjects to both study drugs.
Key words
antihypertensive drugs - bioequivalence - CAS 138402-11-6 - irbesartan - pharmacokinetics