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Clinical Trial Summary

The purpose of the present trial is to evaluate the safety, tolerability and pharmacokinetics(PK)/pharmacodynamics(PD) of single subcutaneous injection of GW003 in breast cancer patients. Moreover, the efficacy will be assessed preliminary.


Clinical Trial Description

This is an single-center, open-label, randomized, active-controlled phase I study evaluating tolerability and pharmacokinetics/pharmacodynamics of single subcutaneous injections of GW003 in the breast cancer patients.GW003 is recombinant human serum albumin/human granulocyte-colony stimulating factor(I)fusion protein .It is a long-acting G-CSF(Granulocyte-Colony Stimulating Factor). In this study, participants will be administered a single dose of GW003. Every subject will only accept one dose. In addition to tolerability and safety, pharmacokinetics/pharmacodynamics, preliminary efficacy and immunogenicity of GW003 will be evaluated as well. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02725606
Study type Interventional
Source Jiangsu T-Mab Biopharma Co.,Ltd
Contact Xichun Hu
Email xchu2009@hotmail.com
Status Recruiting
Phase Phase 1
Start date March 2016
Completion date September 2017

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