Comparative pharmacodynamic effects of two clopidogrel formulations under steady-state conditions in healthy Thai volunteers

• Published in: International journal of clinical pharmacology and therapeutics Vol. 55; no. 2; pp. 177 - 185
• Main Authors: Nakkam, Nontaya, Tiamkao, Somsak, Kanjanawart, Sirimas, Phunikhom, Kutcharin, Tiamkao, Siriporn, Vannaprasaht, Suda, Tassaneeyakul, Wongwiwat, Tassaneeyakul, Wichittra
• Format: Journal Article
• Language: English
• Published: Germany Dustri - Verlag Dr. Karl Feistle GmbH & Co. KG 01.02.2017
• Subjects: Adenosine diphosphate; Adult; Area Under Curve; Asian People; Blood platelets; Blood Platelets - drug effects; Blood Platelets - metabolism; Clopidogrel; Cross-Over Studies; Drug Compounding; Drug dosages; Drugs, Generic - administration & dosage; Drugs, Generic - pharmacokinetics; Healthy Volunteers; Humans; Male; Manufacturing; Pharmaceutical industry; Pharmacodynamics; Platelet Aggregation - drug effects; Platelet Aggregation Inhibitors - administration & dosage; Platelet Aggregation Inhibitors - blood; Platelet Aggregation Inhibitors - pharmacokinetics; Platelet Function Tests; Purinergic P2Y Receptor Antagonists - administration & dosage; Purinergic P2Y Receptor Antagonists - blood; Purinergic P2Y Receptor Antagonists - pharmacokinetics; Receptors, Purinergic P2Y12 - blood; Receptors, Purinergic P2Y12 - drug effects; Thailand; Therapeutic Equivalency; Ticlopidine - administration & dosage; Ticlopidine - analogs & derivatives; Ticlopidine - blood; Ticlopidine - pharmacokinetics; Young Adult; Thailand
• ISSN: 0946-1965
• DOI: 10.5414/CP202723

Clopidogrel is a commonly used antiplatelet aggregation agent. Compared with the reference clopidogrel product, most commercially available generic clopidogrel products contain different crystalline forms of clopidogrel. This study was aimed to compare the pharmacodynamics of a commonly used generic clopidogrel product in Thailand with the reference clopidogrel product under steady state conditions. A multiple-dose, randomized 2-way crossover study was conducted in 32 healthy male Thai volunteers. The subjects were assigned to receive 75 mg once daily of the test or the reference product for 7 days with a 2-week wash out period. Blood samples were collected on days 1, 5, 6, and 7 prior to drug administration and at 1, 2, 3, 4, 8, 12, and 24 hours after the last dose administered. The antiplatelet aggregation effects of clopidogrel were determined by using two different ex-vivo platelet aggregation tests including the whole blood impedance assay (WBA) and the VerifyNow P2Y12 assay. Both pharmacodynamic parameters, the maximal antiplatelet effect (E ) and the areas under the antiplatelet effect-time curve (AUEC ), were calculated. Neither the mean values of E (90.70 ± 15.15 vs. 89.50 ± 10.71% inhibition) nor of AUEC (1,892.84 ± 657.22 vs. 1,853.58 ± 673.95% inhibition × h) under steady-state conditions obtained using the WBA method of these two clopidogrel products were significantly different. The results obtained using the VerifyNow P2Y12 assay were consistent with those of the WBA assay. This study clearly demonstrated that ex-vivo antiplatelet aggregation effect under steady-state conditions of the test product was not significantly different from the reference product.
.