drugset / Trial / NCT01918852

S-1 Versus Capecitabine in the First Line Treatment of MCC Patients.

NCT01918852

RandomizedParallel-groupOpen-labelTreatment

Summary

The study is a two-arm randomised phase III trial. Patients will be randomised to receive capecitabine (arm A) or S-1 (arm B). Bevacizumab may be added according to the choice of the investigator. Patients will be followed 3-weekly at the outpatient clinic, toxicity will be assessed according to study protocol guidelines. Patients will be evaluated every 3 cycles for response. Upon disease progression patients will be treated according to the local investigators

Timeline

Start
2013-12
Primary completion
2015-12
Completion
2018-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Capecitabine Small molecule 1000 mg/m2
Comparator Capecitabine Small molecule 1250 mg/m2
Subject S-1 Small molecule 30 mg/m2 Oral
Background Bevacizumab Monoclonal antibody 7.5 mg/kg Intravenous