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Indobufen (K 3920), a new inhibitor of platelet aggregation: Effect of food on bioavailability, pharmacokinetic and pharmacodynamic study during repeated oral administration to man

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Summary

The effect of food on bioavailability of indobufen tablets was investigated in 6 healthy volunteers. Subsequently, the same subjects took 100 mg b.i.d. for 7 days. Plasma levels and urinary excretion of indobufen were determined by GLC. Platelet aggregation induced by several concentrations of adrenaline was determined turbidimetrically at various times after the first and last doses. The absorption of indobufen tablets was not substantially impaired by the presence of food in the GI tract, although peak plasma levels and AUCs were slightly reduced after food. Pharmacokinetic analysis of plasma and urinary levels of indobufen did not indicate any change in drug disposition after repeated dosing. Adrenaline-induced platelet aggregation was markedly inhibited for up to 12 h after the first dose and the intensity and duration of this effect did not change after repeated administration. A twice-daily dosing appears suitable for clinical trials.

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References

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  4. Fuccella, L. M., Corvi, G., Moro, E., Pogliani, E., Tamassia, V., Tosolini, G.: Pharmacokinetic, bioavailability and pharmacodynamic study of indobufen (K 3920), inhibitor of platelet aggregation, after single administration in man. Europ. J. clin Pharmacol.15, 323–327 (1979)

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A preliminary account of this study was given at the 4th Meeting of the European and African Division of the International Society of Haematology, Istanbul, 5–9 September 1977.

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Tamassia, V., Corvi, G., Fuccella, L.M. et al. Indobufen (K 3920), a new inhibitor of platelet aggregation: Effect of food on bioavailability, pharmacokinetic and pharmacodynamic study during repeated oral administration to man. Eur J Clin Pharmacol 15, 329–333 (1979). https://doi.org/10.1007/BF00558436

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  • DOI: https://doi.org/10.1007/BF00558436

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