Overview

Clofarabine in High Risk Myelodysplastic Syndrome (MDS)

Status:
Completed
Trial end date:
2014-03-01
Target enrollment:
Participant gender:
Summary
This study aims to determine the maximal tolerated dose (MTD) and dose limiting toxicities (DLTs) of low dose IV clofarabine for MDS patients after treatment failure of azacitidine.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Groupe Francophone des Myelodysplasies
Collaborator:
Genzyme, a Sanofi Company
Treatments:
Clofarabine