drugset / Trial / NCT07202364

A Study of YL202 in Patients With Advanced Solid Tumors

NCT07202364

Phase 2 Recruiting 100 enrolled MediLink Therapeutics (Suzhou) Co., Ltd.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study is a multicenter, open-label, phase II study of YL202 in China to evaluate the efficacy, safety, and PK characteristics of YL202 in selected patients with advanced solid tumors.

Timeline

Start
2025-08-04
Primary completion
2026-08-31
Completion
2027-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject YL202 Unknown 1.6 mg Intravenous