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Clinical Trial Summary

This study is to examine which dose of DA-3031(PEG-G-CSF) has similar efficacy and safety compared to daily G-CSF in chemotherapy-induced neutropenia.


Clinical Trial Description

Eligible subjects are randomly assigned to receive once-per-cycle DA-3031(PEG-G-CSF) or daily G-CSF(up to 10 days). This study is conducted for 1 cycles of chemotherapy. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01923545
Study type Interventional
Source Dong-A ST Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date July 2010
Completion date May 2011

See also
  Status Clinical Trial Phase
Recruiting NCT02787876 - Pegteograstim in Children With Solid Tumors Phase 2
Completed NCT01328938 - GCPGC in Chemotherapy-induced Neutropenia Phase 2/Phase 3
Completed NCT01674855 - Phase III Study of DA-3031(PEG-G-CSF) in Chemotherapy-induced Neutropenia Phase 3