drugset / Trial / NCT03395028

GCSF Adjunct Therapy for Biliary Atresia

NCT03395028

NaSingle-groupOpen-labelSupportive care

Summary

The Investigators propose to test the hypothesis that GCSF therapy enhances the clinical outcome of Kasai operated Biliary Atresia (BA) patients. In this study, Investigators will conduct a dose determination for GCSF use in post Kasai subjects to support a future phase 2 efficacy study. The first 3 post Kasai BA subjects with liver biopsy-confirmed BA will be given 5 ug/kg/d of GCSF in 3 daily subcutaneous doses starting on post Kasai day 3. A second group of 3 subjects will be assigned to the 10 ug/Kg/d dose after the 5ug/kg/d dose has been proven to be safe. The levels of circulating hematopoietic stem cells and a 1-month safety profile will be analyzed.

Timeline

Start
2018-01-15
Primary completion
2020-01-31
Completion
2020-01-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject filgrastim Protein / enzyme biologic 5 ug/kg Subcutaneous
Subject filgrastim Protein / enzyme biologic 10 ug/kg Subcutaneous

Indications