drugset / Trial / NCT00697476

Study of Oral Vorinostat in Combination With Topotecan in Patients With Chemosensitive Recurrent SCLC

NCT00697476

Phase 1/2 Terminated 2 enrolled Armando Santoro, MD
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the maximum tolerated dose, the activity and the safety profile of the combination of vorinostat and topotecan in patients with recurrent small cell lung cancer

Timeline

Start
2009-01
Primary completion
2009-09
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Topotecan Small molecule 1.2 mg/m2 Intravenous
Subject Topotecan Small molecule 1.5 mg/m2 Intravenous
Subject Vorinostat Small molecule 300 mg Oral
Subject Vorinostat Small molecule 400 mg Oral