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Published in: Clinical Drug Investigation 1/2001

01-01-2001 | Clinical Pharmacokinetics

Esomeprazole 40mg Capsules are Bioequivalent when Administered Intact or as the Contents Mixed with Applesauce

Authors: Dr Tommy Andersson, David Magner, Jay Patel, Paul Rogers, Jeffrey G. Levine

Published in: Clinical Drug Investigation | Issue 1/2001

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Abstract

Objective

This study was conducted to determine whether administration of the contents of an open capsule of esomeprazole (enteric-coated pellets) 40mg with applesauce is bioequivalent to administration of an intact capsule in healthy volunteers.

Participants and Study Design

45 adult male and female volunteers participated in this randomised, single-dose, nonblinded, two-way crossover study conducted at a single centre.

Results

41 volunteers completed the trial. Time to maximum plasma concentration (Cmax) for esomeprazole (tmax) was approximately 2.4 hours and elimination half-life (t1/2) was approximately 0.9 hours by either mode of administration. The ratios of the geometric means for Cmax and area under the plasma concentration-time curve (AUC) for capsule contents with applesauce relative to intact capsule were 0.93 (90% confidence interval [CI]: 0.86 to 1.01) and 0.99 (90% CI: 0.94 to 1.04), respectively. The finding that the 90% CIs were within 0.80 to 1.25 for both parameters indicates bioequivalence. Esomeprazole was well tolerated by the study group irrespective of mode of administration.

Conclusions

Esomeprazole is bioequivalent when administered either as an intact capsule or as the contents of a capsule mixed with applesauce in healthy volunteers. This latter alternative mode of administration may provide benefits to patients who have difficulty swallowing.
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Metadata
Title
Esomeprazole 40mg Capsules are Bioequivalent when Administered Intact or as the Contents Mixed with Applesauce
Authors
Dr Tommy Andersson
David Magner
Jay Patel
Paul Rogers
Jeffrey G. Levine
Publication date
01-01-2001
Publisher
Springer International Publishing
Published in
Clinical Drug Investigation / Issue 1/2001
Print ISSN: 1173-2563
Electronic ISSN: 1179-1918
DOI
https://doi.org/10.2165/00044011-200121010-00009

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