drugset / Trial / NCT05048368
Pharmacokinetics Study of Larotinib in Subjects With Impaired Hepatic Function
Non-randomizedParallel-groupOpen-labelTreatment
Summary
To evaluate the pharmacokinetics and safety of Larotinib in subjects with mild and moderate hepatic function impairment and healthy subjects in a single-center, non-randomized, open, single-dose administration
Timeline
- Start
- 2026-10-30
- Primary completion
- 2026-12-30
- Completion
- 2026-12-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Larotinib | Unknown | 350 mg | Oral |