Effects of nirmatrelvir/ritonavir on midazolam and dabigatran pharmacokinetics in healthy participants

被引:12
作者
Cox, Donna S. [1 ,5 ]
Rehman, Muhammad [2 ]
Khan, Tahira [3 ]
Ginman, Katherine [3 ]
Salageanu, Joanne [1 ]
LaBadie, Robert R. [4 ]
Wan, Katty [1 ]
Damle, Bharat [4 ]
机构
[1] Pfizer Inc Global Prod Dev, Collegeville, PA USA
[2] Pfizer Inc Global Prod Dev, Andover, MA USA
[3] Pfizer Inc Global Prod Dev, Groton, CT USA
[4] Pfizer Inc Global Prod Dev, New York, NY USA
[5] Pfizer Inc Global Prod Dev, 500 Arcola Rd, Collegeville, PA 19426 USA
关键词
clinical pharmacology > medication safety; pharmacokinetics > cytochrome P450; pharmacokinetics > drug interactions; pharmacokinetics > p-glycoprotein; CONCISE GUIDE; DRUG-INTERACTION; RITONAVIR; INHIBITOR;
D O I
10.1111/bcp.15835
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
AimsTo evaluate pharmacokinetics (PK) and safety after coadministration of nirmatrelvir/ritonavir or ritonavir alone with midazolam (a cytochrome P450 3A4 substrate) and dabigatran (a P-glycoprotein substrate). MethodsPK was studied in 2 phase 1, open-label, fixed-sequence studies in healthy adults. Single oral doses of midazolam 2 mg (n = 12) or dabigatran 75 mg (n = 24) were administered alone and after steady state (i.e. & GE;2 days) of nirmatrelvir/ritonavir 300 mg/100 mg and ritonavir 100 mg. Midazolam and dabigatran plasma concentrations and adverse events were analysed for each treatment. ResultsAfter administration of midazolam with nirmatrelvir/ritonavir (test) or alone (reference), midazolam geometric mean area under the concentration-time curve extrapolated to infinity (AUC(inf)) and maximum plasma concentration (C-max) increased 14.3-fold and 3.7-fold, respectively. Midazolam coadministered with ritonavir (test) or alone (reference) resulted in 16.5-fold and 3.9-fold increases in midazolam geometric mean AUC(inf) and C-max, respectively. After administration of dabigatran with nirmatrelvir/ritonavir (test) or alone (reference), dabigatran geometric mean AUC(inf) and C-max increased 1.9-fold and 2.3-fold, respectively. Dabigatran coadministered with ritonavir (test) or alone (reference) resulted in a 1.7-fold increase in dabigatran geometric mean AUC(inf) and C-max. Midazolam or dabigatran exposures were generally comparable when coadministered with nirmatrelvir/ritonavir or ritonavir alone, with a slightly higher dabigatran C-max with nirmatrelvir/ritonavir vs. ritonavir alone. Nirmatrelvir/ritonavir was generally safe when administered with or without midazolam or dabigatran. No serious or severe adverse events were reported. ConclusionCoadministration of midazolam or dabigatran with nirmatrelvir/ritonavir increased systemic exposure of midazolam or dabigatran. Midazolam exposures were comparable when coadministered with nirmatrelvir/ritonavir or ritonavir alone, suggesting no incremental effect of nirmatrelvir. Dabigatran C-max was slightly higher when coadministered with nirmatrelvir/ritonavir compared with of ritonavir alone, suggesting a minor incremental effect of nirmatrelvir.
引用
收藏
页码:3352 / 3363
页数:12
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