drugset / Trial / NCT06389006

To Evaluate the Efficacy and Safety of Disitamab Vedotin Combined With Toripalimab Sequential Chemotherapy as Neoadjuvant Treatment in Patients With HR-positive, HER2-low Breast Cancer

NCT06389006 ↗

Phase 2 Recruiting 79 enrolled RemeGen Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of Disitamab Vedotin combined with Toripalimab sequential chemotherapy as in patients with HR-positive, HER2-low breast cancer

Timeline

Start
2024-04-29
Primary completion
2025-06-01
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Disitamab Vedotin for Injection Unknown 2 mg/kg Intravenous
Subject Toripalimab Monoclonal antibody 3 mg/kg Intravenous
Background Cyclophosphamide Other / unclassified 600 mg/m2 Intravenous
Background Epirubicin Small molecule 90 mg/m2 Intravenous

Indications