Chemotherapy-induced Neutropenia Clinical Trial
Official title:
Efficacy and Safety Phase IIb Study of Recombinant Human Serum Albumin/ Granulocyte Colony-Stimulating Factor Fusion Protein for Injection to Prevent Neutrophilic Granulocytopenia Among Chemotherapy Breast Cancer Patients
Evaluation of the efficacy and safety of recombinant human serum albumin / granulocyte-stimulating factor fusion protein for injection to prevent chemotherapy-induced neutropenia
- Brief Protocol: Treat the patients taking Taxotere+Epirubicin +Cyclophosphamide (TEC)
treatment or Taxotere+Epirubicin (TE)treatment chemotherapy with the study medicine or
positive control during the period between two chemotherapy treatments.
- Targeted patients: breast cancer
- Subjects were randomly divided into two groups. The test group received recombinant
human serum albumin / granulocyte thorns for injection Stimulant fusion protein 2.4mg
treatment. Positive control group received recombinant human granulocyte colony stimuli
Factor injection therapy
- Number of patients: 80
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