Ayalasomayajula Surya, Tchaloyan Stéphanie, Yeh Ching-Ming, Bizot Marie-Noelle, Dieterich Hans Armin, Howard Dan, Dole William P
Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Curr Med Res Opin. 2008 Mar;24(3):717-26. doi: 10.1185/030079908X260934. Epub 2008 Jan 29.
Aliskiren is the first in a new class of orally effective direct renin inhibitors approved for the treatment of hypertension. This multiple-dose study investigated the potential for pharmacokinetic interactions between aliskiren and three drugs, each predominantly eliminated by a different clearance/metabolic pathway: allopurinol (glomerular filtration), celecoxib (cytochrome P450 metabolism) and cimetidine (P-glycoprotein and organic anion/cation transporters).
Three open-label, multiple-dose studies in healthy subjects investigated possible pharmacokinetic interactions between aliskiren 300 mg od and allopurinol 300 mg od (n = 20), celecoxib 200 mg bid (n = 22), or cimetidine 800 mg od (n = 22). Subjects received aliskiren alone or co-administered with allopurinol, celecoxib or cimetidine. Allopurinol and celecoxib were also administered alone and in combination with aliskiren. Plasma drug concentrations were determined by LC/MS/MS.
Co-administration of aliskiren with allopurinol had no effect on allopurinol AUC(tau) (ratio of geometric means 0.93 [90% CI, 0.88, 0.98]) or oxypurinol AUC(tau) (mean ratio 1.12 [90% CI, 1.08, 1.16]) and C(max) (mean ratio 1.08 [90% CI, 1.04, 1.13]), with 90% CI within the bioequivalence range 0.80-1.25, and a minor effect on allopurinol C(max) (mean ratio 0.88 [90% CI, 0.78, 1.00]). Aliskiren co-administration had no effect on AUC(tau) or C(max) of celecoxib (mean ratios and 90% CI within range 0.80-1.25). Neither allopurinol nor celecoxib significantly altered aliskiren AUC(tau) or C(max) (geometric mean ratios 0.88-1.02 with 90% CI including 1.00, but with some 90% CI outside the 0.80-1.25 range due to high variability). Co-administration of aliskiren with cimetidine increased aliskiren AUC(tau) by 20% (mean ratio 1.20 [90% CI, 1.07, 1.34]) and C(max) by 25% (mean ratio 1.25 [90% CI, 0.98, 1.59]).
In this multiple-dose study, aliskiren showed no clinically relevant pharmacokinetic interactions when co-administered with allopurinol, celecoxib or cimetidine in healthy subjects.
阿利吉仑是获批用于治疗高血压的新型口服有效的直接肾素抑制剂中的首个药物。这项多剂量研究调查了阿利吉仑与三种药物之间发生药代动力学相互作用的可能性,这三种药物各自主要通过不同的清除/代谢途径消除:别嘌醇(肾小球滤过)、塞来昔布(细胞色素P450代谢)和西咪替丁(P-糖蛋白以及有机阴离子/阳离子转运体)。
三项针对健康受试者的开放标签、多剂量研究调查了阿利吉仑300毫克每日一次与别嘌醇300毫克每日一次(n = 20)、塞来昔布200毫克每日两次(n = 22)或西咪替丁800毫克每日一次(n = 22)之间可能存在的药代动力学相互作用。受试者单独服用阿利吉仑,或与别嘌醇、塞来昔布或西咪替丁联合服用。别嘌醇和塞来昔布也单独给药,并与阿利吉仑联合给药。通过液相色谱/串联质谱法测定血浆药物浓度。
阿利吉仑与别嘌醇联合给药对别嘌醇的AUC(tau)(几何均值比为0.93 [90%置信区间,0.88, 0.98])或氧嘌呤醇的AUC(tau)(平均比值为1.12 [90%置信区间,1.08, 1.16])以及C(max)(平均比值为1.08 [90%置信区间,1.04, 1.13])均无影响,90%置信区间在生物等效性范围0.80 - 1.25内,对别嘌醇的C(max)有轻微影响(平均比值为0.88 [90%置信区间,0.78, 1.00])。阿利吉仑联合给药对塞来昔布的AUC(tau)或C(max)无影响(平均比值和90%置信区间在0.80 - 1.25范围内)。别嘌醇和塞来昔布均未显著改变阿利吉仑的AUC(tau)或C(max)(几何均值比为0.88 - 1.02,90%置信区间包含1.00,但由于高变异性,部分90%置信区间超出0.80 - 1.25范围)。阿利吉仑与西咪替丁联合给药使阿利吉仑的AUC(tau)增加20%(平均比值为1.20 [90%置信区间,1.07, 1.34]),C(max)增加25%(平均比值为1.25 [90%置信区间,0.98, 1.59])。
在这项多剂量研究中,在健康受试者中,阿利吉仑与别嘌醇、塞来昔布或西咪替丁联合给药时未显示出临床相关的药代动力学相互作用。