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Safety and Efficacy of PEG-rhG-CSF in Preventing Neutropenia in Children With Tumor After Chemotherapy

Pediatric Cancer Clinical Trial

Official title:
Safety and Efficacy of Pegylated Recombinant Human Granulocyte-colony Stimulating Factor(PEG-rhG-CSF) in Preventing Neutropenia in Children With Tumor After Chemotherapy：A Multi-center, Single Arm Trial.

Clinical Trial Summary

The purpose is to evaluate the safety of PEG-rhG-CSF in the prevention of neutropenia in children with tumor after chemotherapy, and then evaluate the effectiveness of PEG-rhG-CSF in preventing neutropenia in children with tumor after chemotherapy.

Clinical Trial Description

The dosage was determined according to the patient's weight, 100 UG / kg each time; The method of administration: subcutaneous injection; The time of administration: 24-48 hours after the end of chemotherapy, once in each chemotherapy cycle. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04547829
Study type Interventional
Source Sun Yat-sen University
Contact Yizhuo Zhang
Phone 020-87342459
Email zhangyzh@sysucc.org.cn
Status Recruiting
Phase Phase 2
Start date October 10, 2020
Completion date May 10, 2023
View Details
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