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Clinical Trial Summary

The primary objective of this trial is to compare the progression-free survival (PFS) in two groups of combined therapy of GB221/ capecitabine tablets versus combined therapy of placebo/capecitabine tablets; the secondary objective is to evaluate the objective response rate (ORR),time to progression (TTP) from treatment period to week 12; overall survival (OS), safety, immunogenicity (anti-drug antibody), PFS of subjects during continued treatment period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04164615
Study type Interventional
Source Genor Biopharma Co., Ltd.
Contact Shawn Yu, Master
Phone 18600332657
Email shawn.yu@genorbio.com
Status Recruiting
Phase Phase 3
Start date November 24, 2016
Completion date November 2020