drugset / Trial / NCT00821951

Vorinostat in Combination With Palliative Radiotherapy for Patients With Non-Small Cell Lung Cancer

NCT00821951

Phase 1 Completed 17 enrolled Yale University Merck Sharp & Dohme LLC · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a dose escalation study that will assess the safety of Vorinostat, a Histone Deacetylase (HDAC) inhibitor, in combination with palliative radiotherapy in patients with advanced or metastatic Non-Small Cell Lung Cancer (NSCLC). Vorinostat has been approved for use in patients with cutaneous T-cell lymphomas, but several pre-clinical studies suggest activity in lung cancer cell lines. Several HDAC inhibitors,including Vorinostat, may enhance the effect of radiotherapy, and this study will seek to confirm this.

Timeline

Start
2009-05
Primary completion
2012-07
Completion
2012-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Vorinostat Small molecule 200 mg
Subject Vorinostat Small molecule 300 mg
Subject Vorinostat Small molecule 400 mg