Int. Journal of Clinical Pharmacology and Therapeutics, Volume 49 - July (444 - 450)

Pharmacokinetic-pharmacodynamic equivalence of three gliclazide formulations in healthy human male subjects
A. Samad1, N. Saha2, T. Monif3, P.L. Sharma1, K.K. Pillai1
1 Department of Pharmaceutical Medicine, Faculty of Pharmacy, Hamdard University, 2 Clinical Pharmacology Unit, Ranbaxy Research Laboratories, Majeedia Hospital, Hamdard Nagar, New Delhi, and 3 Clinical Pharmacology and Pharmacokinetcs, Ranbaxy Research Laboratories, Haryana, India

Add to Cart  

 

DOI 10.5414/CP201504

Abstract

Aims: To find out the pharmacokinetic (PK) and pharmacodynamic (PD) parameters for assessing the bioequivalence of three marketed products. To study the relationship between the pharmacokinetics of gliclazide and pharmacodynamic effect in healthy male volunteers. Methods: This was an open label, balanced, randomized, 3-treatment, 3-sequence, 3 period, single-dose, cross-over bioavailability study in which 18 healthy adults were randomized to receive gliclazide 80 mg with 7 days wash out between treatments. The drug was administered with 240 ml of 20% glucose solution after a 10 h overnight fasting. Pharmacokinetic parameters like tmax, Cmax, AUC0–t, AUC0–∞, AUC0–t / AUC0–∞ and t1/2 and pharmacodynamic parameters like maximum effect (minimum glucose level in the body, Cminglu), time to minimum glucose level in the body (Tcminglu) and partial AUC were calculated for all the products. Results: The values for mean ± SD for age, height and weight of the volunteers were 28.00 ± 22.68, 165.78 ± 5.56 and 56.78 ± 13.37 respectively. There were total 4 withdrawn subjects and 1 drop out. Within batch accuracy of the method were in the range of 95.5 – 101.7%, 99.1 – 106.1% and 96.2 – 104.2% for three consecutive batches. The 90% CI for log transformed data of the PK and PD were within the acceptance range of 80.0 – 125.0%. Conclusions: This population PKPD analysis has characterized the relationship between the exposure to gliclazide and its hypoglycemic effect. The test products A & B compared to reference product R were bioequivalent on the basis of pharmacokinetic and pharmacodynamic parameters. Finally it is recommended that the more costly product R can be safely switched with less costly products i.e. A and B.

Author Details

Authors

Departments

  • 1 Department of Pharmaceutical Medicine, Faculty of Pharmacy, Hamdard University,
  • 2 Clinical Pharmacology Unit, Ranbaxy Research Laboratories, Majeedia Hospital, Hamdard Nagar, New Delhi, and
  • 3 Clinical Pharmacology and Pharmacokinetcs, Ranbaxy Research Laboratories, Haryana, India

Address

A. Samad
Department of Pharmaceutical Medicine
Faculty of Pharmacy
Hamdard University
Hamdard Nagar, New Delhi, 110062 India
Email: [email protected]

Citation

A. Samad, N. Saha, T. Monif, P.L. Sharma and K.K. Pillai.Pharmacokinetic-pharmacodynamic equivalence of three gliclazide formulations in healthy human male subjects. 2011; 49: 444-450. doi: 10.5414/CP201504.

###article_not_exists_msg###

Shopping Overview

Shopping Overview
Type Qtty Discount VAT Price
Your basket is empty
View Cart