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Bioequivalence studies of celiprolol in healthy human volunteers.
Indian J Med Sci ; 1996 Jul; 50(7): 234-8
Article in English | IMSEAR | ID: sea-67804
ABSTRACT
Thus bioequivalence between the two products was established by undertaking this study. From table 1 it can be seen that the standard deviation at the various sampling points is high indicating varying absorption rates in individual volunteers, but this was observed in case of both the products. Also, since the study design was complete crossover, this high standard deviation was not due to any study design variable. As celiprolol shows non-linear1 dose related absorption kinetics this high value of standard deviation may be due to the intersubject variation during the absorption process. However all the pharmacokinetic parameters showed a comparable profile when statistically evaluated for any significant difference between the two products.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Male / Therapeutic Equivalency / Double-Blind Method / Celiprolol / Adrenergic beta-Antagonists / Cross-Over Studies / Adult Type of study: Controlled clinical trial Language: English Journal: Indian J Med Sci Year: 1996 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Male / Therapeutic Equivalency / Double-Blind Method / Celiprolol / Adrenergic beta-Antagonists / Cross-Over Studies / Adult Type of study: Controlled clinical trial Language: English Journal: Indian J Med Sci Year: 1996 Type: Article