An open-label, randomized, cross-over bioequivalence study of lafutidine 10 mg under fasting condition

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Oct 6, 2010 (publication date) through Feb 9, 2025

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World Journal of Gastrointestinal Pharmacology and Therapeutics

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2150-5349

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastrointest Pharmacol Ther. Oct 6, 2010; 1(5): 112-118
Published online Oct 6, 2010. doi: 10.4292/wjgpt.v1.i5.112

Table 2 Ratio (Test/Reference), 90% confidence interval and intra-subject variation following the administration of 10 mg lafutidine tablets

Parameters	Ratio (Test/Reference, %)	90% Confidence interval (Log transformed data)	Intrasubject variability (Log transformed data, %)
C_max	106.69	101.86-111.74	9.36
AUC_(0-t)	107.90	102.25-113.86	10.88
AUC_(0-∞)	108.14	102.56-114.03	10.73

AUC: Area under the curve.

Citation: Dewan B, Chimata R. An open-label, randomized, cross-over bioequivalence study of lafutidine 10 mg under fasting condition. World J Gastrointest Pharmacol Ther 2010; 1(5): 112-118
URL: https://www.wjgnet.com/2150-5349/full/v1/i5/112.htm
DOI: https://dx.doi.org/10.4292/wjgpt.v1.i5.112