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Treatment of Breast Cancer With Trastuzumab + HS627/ Pertuzumab + Docetaxel

Breast Cancer Clinical Trial

Official title:
A Phase III Study to Compare HS627 vs. Pertuzumab on the Efficacy, Safety and Immunogenicity in Combination With Trastuzumab and Docetaxel as Neoadjuvant Therapy in Patients With Early-stage or Locally Advanced HER2 Positive Breast Cancer

Clinical Trial Summary

The trial included screening period (4 weeks) and treatment period (4 treatment cycles, at least 12 weeks).

Clinical Trial Description

A multicenter, randomized, double-blind, positive drug parallel control design was used. The trial included screening period (4 weeks) and treatment period (4 treatment cycles, at least 12 weeks). All eligible subjects were randomly divided into experimental group (hs627 treatment group) and control group (pertuzumab) treatment group. After 4 treatment cycles, the subjects arranged surgical treatment, and then conducted the last visit. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04514419
Study type Interventional
Source Zhe Jiang Hisun Bioray Bio-pharmaceu tical Co.Ltd
Contact Anhui Peng, master
Phone 18806555071
Email anhui.peng@hisunbioray.com.cn
Status Recruiting
Phase Phase 3
Start date June 30, 2020
Completion date November 20, 2021
View Details
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