Lefèvre Gilbert, Büche Monika, Sedek Greg, Maton Steve, Enz Albert, Lorch Ulrike, Sagan Cyriaque, Appel-Dingemanse Silke
Novartis Pharma AG, Exploratory Development, WSJ-210.4.25, CH-4002 Basel, Switzerland.
J Clin Pharmacol. 2009 Apr;49(4):430-43. doi: 10.1177/0091270008330161. Epub 2009 Feb 26.
The pharmacokinetics and pharmacodynamics of rivastigmine were compared in Japanese and white healthy participants who were given ascending single doses of the novel rivastigmine transdermal patch. Rivastigmine patch strengths were 4.6 mg/24 h (5 cm2, 9 mg rivastigmine loaded dose), 9.5 mg/24 h (10 cm2, 18 mg), and 13.3 mg/24 h (15 cm2, 27 mg) (per label) or 7.0 mg/24 h (7.5 cm2, 13.5 mg) as a fall-back dose. No relevant ethnic differences in the noncompartmental pharmacokinetics (parent and metabolite NAP226-90) and pharmacodynamics (plasma BuChE activity) of the rivastigmine patch were observed between Japanese and whites. However, drug exposure was slightly higher and inhibition of BuChE slightly more pronounced in Japanese participants than in whites, which was attributed to the lower body weight (ca. 11% less on average) of Japanese participants. Treatments were similarly well tolerated in both ethnic groups. In conclusion, no relevant ethnic differences in the intrinsic disposition or effects of rivastigmine delivered via transdermal route are expected between Japanese and white patients. The possible effect of body weight on drug exposure suggests that special attention should be paid to patients with very low body weight during up-titration.
在日本和白人健康受试者中比较了新型卡巴拉汀透皮贴剂单剂量递增给药后的药代动力学和药效学。卡巴拉汀贴剂的规格为4.6 mg/24 h(5 cm²,载药量9 mg卡巴拉汀)、9.5 mg/24 h(10 cm²,18 mg)和13.3 mg/24 h(15 cm²,27 mg)(按标签),或作为备用剂量的7.0 mg/24 h(7.5 cm²,13.5 mg)。在日本人和白人之间,未观察到卡巴拉汀贴剂的非房室药代动力学(母体和代谢物NAP226 - 90)和药效学(血浆丁酰胆碱酯酶活性)存在相关种族差异。然而,日本受试者的药物暴露量略高于白人,对丁酰胆碱酯酶的抑制作用也略强于白人,这归因于日本受试者体重较低(平均低约11%)。两个种族对治疗的耐受性相似。总之,预计日本和白人患者经皮给药的卡巴拉汀在内在处置或效应方面不存在相关种族差异。体重对药物暴露的可能影响表明,在剂量滴定期间,应特别关注体重极低的患者。