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Clinical Trial Summary

A randomised phase III, double-blind, placebo-controlled trial with 2:1 (regorafenib : placebo)


Clinical Trial Description

Purpose: The purpose of this Phase III study is to determine if regorafenib improves overall survival in patients with Advanced Gastro-Oesophageal Carcinoma. Who is it for: You may be eligible to join this study if you are aged 18 years or above and have been diagnosed with advanced (metastatic or locally recurrent) Gastro-Oesophageal Carcinoma which has not responded to a minimum of 2 lines of prior anti-cancer therapy. Trial Details: Participants will be randomly (by chance) allocated to one of two groups: regorafenib or placebo in 2:1 ratio respectively and will not be aware of their group allocation. Regorafenib or matching placebo will be self-administered by participants orally once daily on days 1-21 of each 28 days cycle. Treatment will continue until disease progression or prohibitive toxicity. Participants will be followed up every 2-4 weeks in order to evaluate their progress on the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02773524
Study type Interventional
Source Australasian Gastro-Intestinal Trials Group
Contact
Status Active, not recruiting
Phase Phase 3
Start date November 2016
Completion date December 2022

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