drugset / Trial / NCT03692520

Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of SCT200 in Patients With Advanced Solid Tumors

NCT03692520

Phase 1 Unknown 90 enrolled Sinocelltech Ltd.
NaSingle-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 solid tumors treated after failure of standard therapy.

Timeline

Start
2018-09-30
Primary completion
2019-11-30
Completion
2020-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject SCT200 Monoclonal antibody 8 mg/kg

Indications