drugset / Trial / NCT07197827

A Study of YL242 in Subjects With Advanced Solid Tumors

NCT07197827

Phase 1/2 Recruiting 424 enrolled MediLink Therapeutics (Suzhou) Co., Ltd.
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a multicenter, open-label study to evaluate the safety and tolerability of YL242 monotherapy and combination in participants with advanced solid malignant tumors.

Timeline

Start
2025-09-22
Primary completion
2028-09
Completion
2028-11

Drugs

EvaluationDrugModalityDoseRoute
Subject LV Unknown Intravenous
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous
Subject YL242 Unknown Intravenous
Subject fluorouracil Small molecule Intravenous

Indications