drugset / Trial / NCT02447419

Study to Evaluate the Safety and Efficacy of Gefitinib, in Subjects With EFGR Amplification Refractory Solid Tumors

NCT02447419 ↗

Phase 2 Completed 16 enrolled Samsung Medical Center
NaSingle-groupOpen-labelTreatment

Summary

This study is a single-arm,phase II study of gefitinib in patient with epidermal growth factor receptor amplification Refractory solid tumors. Gefitinib 250 mg will be administered orally daily. To investigate the efficacy and safety of gefitinib in patient with epidermal growth factor receptor amplification Refractory solid tumors.

Timeline

Start
2014-12-03
Primary completion
2020-06
Completion
2020-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Gefitinib Small molecule 250 mg Oral

Indications