drugset / Trial / NCT04605575

Pyrotinib Plus Vinorelbine in Participants With HER2-positive Previously Treated Locally Advanced or Metastatic Breast Cancer

NCT04605575 ↗

Phase 2 Unknown 208 enrolled Sun Yat-sen University
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to identify the highest tolerable dose of pyrotinib in combination with vinorelbine and to assess the safety and efficacy of the combination in Patients With HER2-Positive Locally Advanced or Metastatic Breast Cancer. The study will be conducted in two parts. In the first part, testing will be done on up to 12 subjects to determine the highest tolerable dose of pyrotinib and vinorelbine in patients with advanced solid tumors. In the second part of the study, we will explore the safety and efficacy of Pyrotinib + vinorelbine in Patients With HER2-Positive Locally Advanced or Metastatic Breast Cancer Who Have Received Prior Trastuzumab-Based Therapy. Participants will be treated until disease progression (PD), unmanageable toxicity, or study termination.

Timeline

Start
2020-05-22
Primary completion
2023-08-01
Completion
2023-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Pyrotinib Small molecule 320 mg Oral
Subject Pyrotinib Small molecule 400 mg Oral
Subject Vinorelbine Small molecule 25 mg/m2 Oral
Subject Vinorelbine Small molecule 80 mg/m2 Oral