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RECRUITING
NCT07186452
PHASE1

Evaluation of the Effect of Itraconazole on the Pharmacokinetics of HS-20093 in Patients With Advanced Solid Tumors

Sponsor: Hansoh BioMedical R&D Company

View on ClinicalTrials.gov

Summary

The primary objective of this study is to evaluate the effect of itraconazole on the pharmacokinetics of HS-20093 in patients with advanced solid tumors.

Official title: A Study to Evaluate the Effect of Itraconazole on the Pharmacokinetics of HS-20093 in Patients With Advanced Solid Tumors Who Have Failed Adequate Standard Treatments or Are Intolerant to Standard Therapies

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

18

Start Date

2025-09-23

Completion Date

2026-08-31

Last Updated

2026-01-16

Healthy Volunteers

No

Interventions

DRUG

HS-20093

All participants will receive intravenous infusion of HS-20093 at a dose of 8 mg/kg every 3 weeks (Q3W), with each treatment cycle lasting 21 days.

DRUG

Itraconazole

Participants will then take itraconazole capsules orally at 200 mg per dose during C2D17-C3D21

Locations (1)

Hunan Cancer Hospital

Changsha, Hunan, China