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No need to adjust the dose of 311C90 (zolmitriptan), a novel anti-migraine treatment, in patients with renal failure not requiring dialysis.

作者信息

Gillotin C, Bagnis C, Mamet J P, Peck R W, Deray G

机构信息

Department of Clinical Pharmacology, Laboratoire Glaxo Wellcome, Issy-les-Moulineaux, France.

出版信息

Int J Clin Pharmacol Ther. 1997 Nov;35(11):522-6.

PMID:9401835
Abstract

311C90 ("Zomig", zolmitriptan), is a novel and selective, centrally and peripherally acting 5 HT1B/1D receptor agonist in development for the acute, oral treatment of migraine. We have conducted a parallel group study in patients with moderate/severe renal impairment (creatinine clearance < or = 40 ml/min) and age- and sex-matched healthy volunteers (creatinine clearance > or = 60 ml/min). All subjects received a single, 10 mg dose of 311C90. Mean peak concentrations of 311C90 and its pharmacologically active N-desmethyl metabolite (183C91) were similar in both groups although AUC0-infinity for 183C91 was increased by 35% in the renally impaired patients. Other pharmacokinetic parameters were little changed apart from the expected reduction in CLR and urinary recovery and a small increase of 0.9 and 1.0 h, respectively, in the mean half-lives of 311C90 and 183C91. For the 2 inactive metabolites, the N-oxide (1652W92) and the indolacetic acid (2161W92), mean peak concentrations were approximately 3 times higher in renally impaired patients than in healthy volunteers and AUC0-infinity was 6-7.5 times higher. CLR for these metabolites was approximately 90% lower in renal impairment and half-life of both was increased approximately 3-fold. Baseline blood pressures were higher in the renally impaired group. After 311C90 there was a transient, small increase in blood pressure in both groups. There was little difference in the increase in diastolic blood pressure between the groups (16 mmHg in both) but the rise in systolic blood pressure was greater in the renally impaired group (23 mmHg vs 16 mmHg in healthy subjects). The lack of substantial changes in the plasma concentrations of both parent compound and 183C91, and the similarity of the changes in blood pressure, in renally impaired subjects compared to healthy volunteers suggest that there is no reason to adjust the dose of 311C90 in patients with renal impairment.

摘要

相似文献

1
No need to adjust the dose of 311C90 (zolmitriptan), a novel anti-migraine treatment, in patients with renal failure not requiring dialysis.
Int J Clin Pharmacol Ther. 1997 Nov;35(11):522-6.
2
The pharmacodynamics and pharmacokinetics of the 5HT1B/1D-agonist zolmitriptan in healthy young and elderly men and women.
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3
The long-term tolerability and efficacy of oral zolmitriptan (Zomig, 311C90) in the acute treatment of migraine. An international study. The International 311C90 Long-term Study Group.口服佐米曲普坦(佐米格,311C90)用于偏头痛急性治疗的长期耐受性和疗效。一项国际研究。国际311C90长期研究组。
Headache. 1998 Mar;38(3):173-83.
4
The absolute bioavailability and metabolic disposition of the novel antimigraine compound zolmitriptan (311C90).新型抗偏头痛化合物佐米曲普坦(311C90)的绝对生物利用度和代谢情况
Br J Clin Pharmacol. 1997 Jun;43(6):579-87. doi: 10.1046/j.1365-2125.1997.00614.x.
5
The pharmacokinetics and effects on blood pressure of multiple doses of the novel anti-migraine drug zolmitriptan (311C90) in healthy volunteers.新型抗偏头痛药物佐米曲坦(311C90)多次给药在健康志愿者体内的药代动力学及对血压的影响。
Br J Clin Pharmacol. 1997 Mar;43(3):273-81. doi: 10.1046/j.1365-2125.1997.00547.x.
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Potential drug interactions with the novel antimigraine compound zolmitriptan (Zomig, 311C90).新型抗偏头痛化合物佐米曲普坦(佐米格,311C90)可能存在的药物相互作用。
Cephalalgia. 1997 Oct;17 Suppl 18:21-7. doi: 10.1177/0333102497017S1804.
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The novel anti-migraine compound zolmitriptan (Zomig 311C90) has no clinically significant interactions with paracetamol or metoclopramide.
Eur J Clin Pharmacol. 1997;53(3-4):229-34. doi: 10.1007/s002280050367.
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[Safety profile of 311C90 (zolmitriptan)].
Neurologia. 1998 Oct;13 Suppl 2:25-30.
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Zolmitriptan.佐米曲普坦
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The interaction between propranolol and the novel antimigraine agent zolmitriptan (311C90).普萘洛尔与新型抗偏头痛药物佐米曲普坦(311C90)之间的相互作用。
Br J Clin Pharmacol. 1997 Dec;44(6):595-9. doi: 10.1046/j.1365-2125.1997.t01-1-00632.x.

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