期刊
CLINICAL KIDNEY JOURNAL
卷 14, 期 7, 页码 1808-1816出版社
OXFORD UNIV PRESS
DOI: 10.1093/ckj/sfaa222
关键词
drug interactions; gastric pH-sensitive drugs; hyperkalemia; pharmacokinetic analysis; sodium zirconium cyclosilicate
资金
- ZS Pharma, Inc.
The study assessed potential pharmacokinetic interactions between sodium zirconium cyclosilicate (SZC) and nine pH-sensitive drugs, showing small changes in plasma concentration and exposure of five of the nine drugs evaluated. These PK drug interactions are consistent with transient increases in gastric pH with SZC and are unlikely to be clinically meaningful.
Background. Sodium zirconium cyclosilicate (SZC; formerly ZS-9) is an oral potassium binder for the treatment of hyperkalemia in adults. SZC acts in the gastrointestinal tract and additionally binds hydrogen ions in acidic environments like the stomach, potentially transiently increasing gastric pH and leading to drug interactions with pH-sensitive drugs. This study assessed potential pharmacokinetic (PK) interactions between SZC and nine pH-sensitive drugs. Methods. In this single-dose, open-label, single-sequence cross-over study in healthy adults, amlodipine, atorvastatin, clopidogrel, dabigatran, furosemide, glipizide, levothyroxine, losartan or warfarin were each administered alone and, following a washout interval, with SZC 10 g. Maximum plasma concentration (C-max), area under the plasma concentration-time curve from 0 to the last time point (AUC(0-t)) and AUC extrapolated to infinity (AUC(inf)) were evaluated. No interaction was concluded if the 90% confidence interval for the geometric mean ratio (SZC coadministration versus alone) of the PK parameters was within 80-125%. Results. During SZC coadministration, all PK parameters for amlodipine, glipizide, levothyroxine and losartan showed no interaction, while reductions in clopidogrel and dabigatran C-max, AUC(0-t) and AUC(inf) (basic drugs) were <50% and increases in atorvastatin, furosemide and warfarin C-max (acidic drugs) exceeded the no-interaction range by <2-fold. Conclusions. SZC coadministration was associated with small changes in plasma concentration and exposure of five of the nine drugs evaluated in this study. These PK drug interactions are consistent with transient increases in gastric pH with SZC and are unlikely to be clinically meaningful.
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