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Randomized clinical trial of the iron-based phosphate binder PA21 in hemodialysis patients.随机临床试验铁基磷酸盐结合剂 PA21 在血液透析患者中的应用。
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Nephron Clin Pract. 2012;121(1-2):c25-9. doi: 10.1159/000341922. Epub 2012 Oct 16.
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Serum levels of phosphorus, parathyroid hormone, and calcium and risks of death and cardiovascular disease in individuals with chronic kidney disease: a systematic review and meta-analysis.血清磷、甲状旁腺激素、钙水平与慢性肾脏病患者死亡和心血管疾病风险的关系:系统评价和荟萃分析。
JAMA. 2011 Mar 16;305(11):1119-27. doi: 10.1001/jama.2011.308.
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The roles of the skeleton and phosphorus in the CKD mineral bone disorder.骨骼和磷在 CKD 矿物质骨代谢紊乱中的作用。
Adv Chronic Kidney Dis. 2011 Mar;18(2):98-104. doi: 10.1053/j.ackd.2011.01.001.
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Medication issues in older individuals with CKD.老年慢性肾脏病患者的药物问题。
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PA21: a novel phosphate binder for the treatment of hyperphosphatemia in chronic kidney disease.PA21:一种用于治疗慢性肾脏病高磷血症的新型磷结合剂。
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Strategies for reducing polypharmacy and other medication-related problems in chronic kidney disease.减少慢性肾脏病中多重用药及其他药物相关问题的策略。
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Phosphate - the silent stealthy cardiorenal culprit in all stages of chronic kidney disease: a systematic review.磷酸盐——慢性肾脏病各阶段隐匿的心脏和肾脏损害元凶:一项系统综述
Blood Purif. 2009;27(2):220-30. doi: 10.1159/000197562. Epub 2009 Jan 29.
9
Mortality risk for dialysis patients with different levels of serum calcium, phosphorus, and PTH: the Dialysis Outcomes and Practice Patterns Study (DOPPS).不同血清钙、磷和甲状旁腺激素水平的透析患者的死亡风险:透析结局和实践模式研究(DOPPS)
Am J Kidney Dis. 2008 Sep;52(3):519-30. doi: 10.1053/j.ajkd.2008.03.020. Epub 2008 Jun 2.
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Bioavailability and bioequivalence of two enteric-coated formulations of omeprazole in fasting and fed conditions.空腹和进食条件下两种奥美拉唑肠溶片的生物利用度和生物等效性。
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健康受试者中氢氧化氧铁蔗糖与氯沙坦、呋塞米、奥美拉唑、地高辛和华法林之间的药物相互作用。

Drug-drug interactions between sucroferric oxyhydroxide and losartan, furosemide, omeprazole, digoxin and warfarin in healthy subjects.

作者信息

Chong Edward, Kalia Veena, Willsie Sandra, Winkle Peter

机构信息

Vifor Pharma, Clinical Development, Aspreva International Ltd., 1203, 4464 Markham Street, Victoria, BC, V8Z 7X8, Canada.

PRA International, Lenexa, KS, USA.

出版信息

J Nephrol. 2014 Dec;27(6):659-66. doi: 10.1007/s40620-014-0080-1. Epub 2014 Apr 4.

DOI:10.1007/s40620-014-0080-1
PMID:24699894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4242982/
Abstract

BACKGROUND

The novel iron-based phosphate binder sucroferric oxyhydroxide is being investigated for the treatment of hyperphosphatemia. Patients with chronic kidney disease often have multiple comorbidities that may necessitate the daily use of several types of medication. Therefore, the potential pharmacokinetic drug-drug interactions between sucroferric oxyhydroxide and selected drugs commonly taken by dialysis patients were investigated.

METHODS

Five Phase I, single-center, open-label, randomized, three-period crossover studies in healthy volunteers investigated the effect of a single dose of sucroferric oxyhydroxide 1 g (based on iron content) on the pharmacokinetics of losartan 100 mg, furosemide 40 mg, omeprazole 40 mg, digoxin 0.5 mg and warfarin 10 mg. Pharmacokinetic parameters [including area under the plasma concentration-time curve (AUC) from time 0 extrapolated to infinite time (AUC0-∞) and from 0 to 24 h (AUC0-24)] for these drugs were determined: alone in the presence of food; with sucroferric oxyhydroxide in the presence of food; 2 h after food and sucroferric oxyhydroxide administration.

RESULTS

Systemic exposure based on AUC0-∞ for all drugs, and AUC0-24 for all drugs except omeprazole (for which AUC 0-8 h was measured), was unaffected to a clinically significant extent by the presence of sucroferric oxyhydroxide, irrespective of whether sucroferric oxyhydroxide was administered with the drug or 2 h earlier.

CONCLUSIONS

There is a low risk of drug-drug interactions between sucroferric oxyhydroxide and losartan, furosemide, digoxin and warfarin. There is also a low risk of drug-drug interaction with omeprazole (based on AUC0-∞ values). Therefore, sucroferric oxyhydroxide may be administered concomitantly without the need to adjust the dosage regimens of these drugs.

摘要

背景

新型铁基磷酸盐结合剂氢氧化氧铁蔗糖目前正在进行治疗高磷血症的研究。慢性肾病患者通常合并多种疾病,这可能需要每日使用多种类型的药物。因此,研究了氢氧化氧铁蔗糖与透析患者常用的特定药物之间潜在的药代动力学药物相互作用。

方法

五项针对健康志愿者的I期、单中心、开放标签、随机、三周期交叉研究,调查了单剂量1 g氢氧化氧铁蔗糖(基于铁含量)对100 mg氯沙坦、40 mg呋塞米、40 mg奥美拉唑、0.5 mg地高辛和10 mg华法林药代动力学的影响。测定了这些药物的药代动力学参数[包括从时间0外推至无限时间的血浆浓度-时间曲线下面积(AUC)(AUC0-∞)以及从0至24小时的AUC(AUC0-24)]:单独在有食物的情况下;在有食物的情况下与氢氧化氧铁蔗糖一起;在进食和服用氢氧化氧铁蔗糖2小时后。

结果

无论氢氧化氧铁蔗糖是与药物同时给药还是提前2小时给药,基于AUC0-∞的所有药物以及除奥美拉唑外所有药物的AUC0-24(测定的是奥美拉唑的AUC 0-8小时)的全身暴露在临床上均未受到显著影响。

结论

氢氧化氧铁蔗糖与氯沙坦、呋塞米、地高辛和华法林之间药物相互作用的风险较低。与奥美拉唑(基于AUC0-∞值)的药物相互作用风险也较低。因此,氢氧化氧铁蔗糖可以与这些药物同时给药,无需调整这些药物的给药方案。