drugset / Trial / NCT00455351

Vorinostat and Palliative Radiotherapy

NCT00455351

Phase 1 Completed 15 enrolled Oslo University Hospital
NaSingle-groupOpen-labelTreatment

Summary

Phase I study. Side-effects when combined with standard palliative radiotherapy.

Timeline

Start
2007-02
Primary completion
2009-03
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Vorinostat Small molecule 100 mg Oral
Subject Vorinostat Small molecule 200 mg Oral
Subject Vorinostat Small molecule 300 mg Oral
Subject Vorinostat Small molecule 400 mg Oral

Indications

No indication recorded.