drugset / Trial / NCT03808701

Efficacy and Safety of SCT200 in Patients With Advanced Squamous Non-small Cell Lung Cancer

NCT03808701

Phase 1 Unknown 50 enrolled Sinocelltech Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of recombinant anti-EGFR monoclonal antibody(SCT200)in patients with advanced squamous non-small cell lung cancer treated after failure of Two chemotherapy regimens (including Platinum-based drugs).

Timeline

Start
2019-03
Primary completion
2019-12
Completion
2019-12

Drugs

EvaluationDrugModalityDoseRoute
Subject SCT200 Monoclonal antibody 12 mg/kg
Subject SCT200 Monoclonal antibody 15 mg/kg