drugset / Trial / NCT04009941

Efficacy and Safety of 4.5mg PEG-rhG-CSF Per Cycle in Preventing Neutropenia After Intensive Chemotherapy for Breast Cancer

NCT04009941

Phase 4 Completed 104 enrolled Peking University
NaSingle-groupOpen-labelPrevention

Summary

This is a prospective, single-center, single-arm clinical study, to evaluate the clinical efficacy, safety and tolerance of patients with early breast cancer receiving ddEC adjuvant chemotherapy, accepting PEG-rhG-CSF as primary prevention of neutropenia.

Timeline

Start
2019-08-01
Primary completion
2020-01-18
Completion
2020-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Pegfilgrastim Protein / enzyme biologic 4.5 mg