# Effect of itraconazole on pharmacokinetics of ZX-7101A tablets in healthy Chinese subjects

**Authors:** Junzhen Wu, Yin Wang, Wei Liu, Jinjie He, Jufang Wu, Jicheng Yu, Xiaojie Wu, Jianguang Su, Mei Liu, Yilin Li, Jing Zhang

PMC · DOI: 10.3389/fphar.2025.1722747 · Frontiers in Pharmacology · 2025-12-18

## TL;DR

This study found that itraconazole increases the levels of ZX-7101 in the blood, but no dose adjustment is needed when taken together.

## Contribution

The study provides new pharmacokinetic data on the interaction between itraconazole and ZX-7101A in healthy Chinese subjects.

## Key findings

- Itraconazole increased ZX-7101's Cmax, AUC0-t, and AUC0-inf by 29.5%, 53.7%, and 58.0%, respectively.
- The half-life of ZX-7101 was prolonged by 17.6% when coadministered with itraconazole.
- ZX-7101 exposure with itraconazole was lower than a single 80 mg dose, so no dose adjustment is needed.

## Abstract

A single-center, open label trial was conducted to evaluate the effects of itraconazole on the pharmacokinetics of ZX-7101A tablets in healthy Chinese adults.

Subjects took a single dose of 40 mg ZX-7101A tablets on Day 1 on Day 31following once-daily itraconazole administration (200 mg, Days 26–50). The concentrations of ZX-7101A and ZX-7101 in plasma samples were determined by liquid chromatography–tandem mass spectrometry. Pharmacokinetic (PK) parameters of ZX-7101A and ZX-7101 were calculated, and the effects of itraconazole on the PK of ZX-7101 were evaluated.

The median Tmax of ZX-7101 was 4 h. In stage 1, the mean (±SD) Cmax, AUC0-t, AUC0-inf, and t1/2 of ZX-7101 were 90.86 ± 44.48 ng/mL, 6313.72 ± 1095.17 h*ng/mL, 6827.31 ± 1163.30 h*ng/mL, and 126.40 ± 28.88 h, respectively. In stage 2, the corresponding values were 117.63 ± 29.95 ng/mL, 9706.83 ± 1062.56 h*ng/mL, 10785.99 ± 1389.08 h*ng/mL, and 148.62 ± 28.72 h. Itraconazole increased ZX-7101 Cmax, AUC0-t, and AUC0-inf by 29.5%, 53.7%, and 58.0%, respectively, and prolonged t1/2 of ZX-7101 by 17.6%.

The ZX-7101 exposure after coadministration with itraconazole is lower than the exposure after a single dose of 80 mg ZX-7101A tablets. It is therefore not necessary to adjust the dose of ZX-7101A 40 mg when coadministered with itraconazole.

http://www.chinadrugtrials.org.cn, identifier: CTR20231556.

## Linked entities

- **Chemicals:** itraconazole (PubChem CID 55283)

## Full-text entities

- **Chemicals:** Itraconazole (MESH:D017964), ZX-7101 (-)

## Full text

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## Figures

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12756401/full.md

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Source: https://tomesphere.com/paper/PMC12756401