Key result
Pentacard 20 mg tablets and Ismo 20 mg tablets were judged to be bioequivalent based on pharmacokinetic parameters after single and multiple dosing.
Why the study?
Are Pentacard 20 mg tablets bioequivalent to Ismo 20 mg tablets in healthy volunteers?
RCT (n=12)
Open-label
randomized, two-way crossover
Are Pentacard 20 mg tablets bioequivalent to Ismo 20 mg tablets in healthy volunteers?
Pentacard 20 mg tablets and Ismo 20 mg tablets are bioequivalent in healthy volunteers.
Answers are grounded in this paper and cite their sources.
Supports interchangeability of Pentacard and Ismo in practice; confirms bioequivalence by RCT in healthy volunteers.
Pharmacokinetics of 20 mg isosorbide-5-mononitrate (IS-5-MN) after single and multiple administration of two different tablet formulations were investigated in twelve healthy human subjects using an open, randomized, two-way crossover experimental design. Pentacard 20 mg tablets were compared with Ismo 20 mg tablets. After single-dose administration, both preparations caused a rapid increase in IS-5-MN plasma levels with the peak plasma concentration occurring between 0.5 and 1.5 h. For both formulations, the mean plasma half-life was found to be approximately 5 h after a single dose. In steady state during multiple dosing (t.i.d. at 8 h dosing intervals), a reduced elimination rate was observed. In line with this observation, the area under the plasma concentration-time curve (AUC) for one 8 h dosing interval during multiple dosing was higher than the extrapolated AUC after a single dose. Based on statistical evaluation of the various relevant pharmacokinetic parameters calculated from the plasma concentrations occurring after single and multiple dosing, the tablet formulations are judged to be bioequivalent.
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Storm et al. (1991) conducted an RCT in Healthy volunteers (n=12). Pentacard (isosorbide-5-mononitrate) vs. Ismo 20 mg tablets was evaluated on Bioequivalence based on pharmacokinetic parameters. Pentacard 20 mg tablets and Ismo 20 mg tablets were judged to be bioequivalent based on pharmacokinetic parameters after single and multiple dosing.
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