Overview

Erlotinib in Higher Risk Myelodysplastic Syndrome

Status:
Completed
Trial end date:
2014-03-01
Target enrollment:
Participant gender:
Summary
The aim of this study is to evaluate the toxicity and therapeutic efficacy of erlotinib in high-risk myelodysplastic syndrome (MDS) patients (with at least 10% of bone marrow blasts) ineligible for or having failed intensive chemotherapy and ineligible or after failure of treatment with a hypomethylating agent.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Groupe Francophone des Myelodysplasies
Collaborator:
Roche Pharma AG
Treatments:
Erlotinib Hydrochloride