1 Minimum, maximum 1.3, 4.9 3, 30 38.5, 218.4 12.7, this website 55.2 0.25, 1.3 8.9, 34.7 Summary of d-MPH pharmacokinetic parameters, pharmacokinetic population MPH alone N 38 38 32 32 32 32 Mean [SD] 9.9
[2.8] 6.9 [1] 102.8 [34.6] 3.9 [0.7] 5.1 [1.7] 28.8 [11.6] Median 10.1 6 100.2 3.8 4.9 24.1 Minimum, maximum 5.1, 16.0 6, 8.1 50.2, 216.3 2.9, 5.7 2.2, 8.7 15.9, 71.3 GXR + MPH N 37 37 32 32 32 32 Mean [SD] 9.5 [2.9] 7.4 [1.3] 100.5 [33] 4.1 [0.6] 5.0 [1.4] 28.6 [7.1] Median 8.8 8 94.9 4 5.2 28.5 Minimum, maximum 5.4, 18.2 6, 12 57.6, 215.7 3.1, 5.3 2.2, 7.2 15.2, 40.2 Summary of l-MPH pharmacokinetic parameters, pharmacokinetic population MPH alone N 38 13 38 0 0 0 Mean [SD] 0.2 [0.3] 6.5 [0.9] 0.5 [0.9] – – – Median 0 6 0
– – – Minimum, maximum 0, 0.9 6, 8 0, 4.2 – – – GXR + MPH N 37 9 37 0 0 0 Mean [SD] 0.2 [0.5] 6.4 [0.9] 0.7 [2.0] – – – Median 0 6 0 – – – Minimum, maximum 0, 2.6 6, 8 0, 11 – – – AUC ∞ area under the plasma concentration–time curve extrapolated to infinity, CL/F apparent oral-dose clearance, C max maximum plasma concentration, GXR guanfacine extended release, MPH methylphenidate hydrochloride, SD standard deviation, t ½ apparent elimination half-life, t max time to Cmax, V λz /F apparent volume of distribution during the terminal phase after oral administration The mean plasma guanfacine concentrations Selleckchem Capmatinib following administration of GXR alone and in combination with MPH are shown in Fig. 1. these No noteworthy differences in guanfacine Cmax, AUC∞, and bodyweight-normalized CL/F and Vλz/F were noted after administration of GXR alone or in combination with MPH. The 90 % CIs of the GMRs for Cmax and AUC∞ for guanfacine following GXR alone or
in combination with MPH met strict bioequivalence buy I-BET-762 criteria requiring 90 % CIs to fall within the interval of 0.80–1.25 (Cmax GMR 1.065, 90 % CI 0.945–1.200; AUC∞ GMR 1.109, 90 % CI 0.997–1.235), indicating that GXR alone and GXR in combination with MPH met the criteria for bioequivalence. Fig. 1 Mean plasma guanfacine concentrations over time following administration of guanfacine extended release (GXR) alone and in combination with methylphenidate hydrochloride (MPH). A time shift has been applied to the figure; values have been slightly staggered on the x-axis for clarity, as some values were similar between the two treatment regimens The mean plasma concentrations of d-MPH following administration of MPH alone and in combination with GXR are shown in Fig. 2. Maximum plasma concentrations of d-MPH were observed at a median of 6 h when MPH was administered alone and at 8 h when MPH was administered in combination with GXR (Table 2).