drugset / Trial / NCT05653752

A Study of YL202 in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer and Breast Cancer

NCT05653752

Phase 1 Active not recruiting 80 enrolled MediLink Therapeutics (Suzhou) Co., Ltd. BioNTech SE · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a phase 1, multicenter, open-label, first-in-human study of YL202 conducted in the United States and China. The study will evaluate the safety and tolerability of YL202 in patients with locally advanced or metastatic epidermal growth factor receptor (EGFR)-mutated NSCLC or hormone receptor (HR)-positive and HER2-negative BC, which have been heavily treated by standard treatment.

Timeline

Start
2022-12-20
Primary completion
2026-12
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject YL202 Unknown Intravenous