| Autor: |
Shuchean Chien, Caiping Yao, Mertens, Annemie, Verhaeghe, Tom, Solanki, Bhavna, Doose, Dennis R., Novak, Gerald, Bialer, Meir |
| Předmět: |
|
| Zdroj: |
Epilepsia (Series 4); Jul2007, Vol. 48 Issue 7, p1328-1338, 11p, 1 Diagram, 6 Charts, 5 Graphs |
| Abstrakt: |
Purpose: To characterize possible pharmacokinetic interactions between the new antiepileptic drug carisbamate (RWJ-333369) and valproic acid (VPA) or lamotrigine (LTG) following multiple dosing in healthy subjects. Methods: Two open-label, sequential-design studies were conducted in 24 healthy adults. In Study 1, subjects received carisbamate alone (5 days 250 mg q12h; 5 days 500 mg q12h), then VPA alone (7 days 300 mg q12h; 7 days 500 mg q12h), and then a combination of VPA (500 mg q12h) and carisbamate (5 days 250 mg q12h; 5 days 500 mg q12h). In Study 2, subjects received carisbamate alone as in Study 1, then LTG alone (14 days 25 mg q12h; 14 days 50 mg q12h), and then combination of LTG (50 mg q12h) and carisbamate (3 days 250 mg q12h; 14 days 500 mg q12h). Results: Coadministration of VPA or LTG had minimal effect on carisbamate mean Cmax and AUCss values. Mean VPA-Cmax and AUCss values were ∼15% lower when given concomitantly with carisbamate. However, the 90% confidence intervals (CIs) for the Cmax and AUCss ratio with/without carisbamate were within the 80–125% equivalence range, Cmax 82–89%; AUCss 81–88%. Mean LTG Cmax and AUCss values were ∼20% lower when given concomitantly with carisbamate. The 90% CIs with and without carisbamate for LTG Cmax and AUCss were 79–86% and 75–81%, respectively. This modest change is not considered clinically significant. Conclusions: There were no clinically significant interactions between carisbamate and VPA or LTG. Concomitant administration of carisbamate with VPA or LTG was generally safe and well tolerated. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
Plný text