Overview

Vorinostat and Low Dose Cytarabine for High Risk Myelodysplasia

Status:
Completed
Trial end date:
2011-11-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to determine the maximum tolerated duration and schedule of oral VORINOSTAT in addition to low dose cytarabine in the treatment of Intermediate-2 and High risk myelodysplastic syndromes.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Groupe Francophone des Myelodysplasies
Collaborator:
Merck Sharp & Dohme Corp.
Treatments:
Cytarabine
Vorinostat