Overview

Study of Clinical Efficacy and Safety of Tosedostat in MDS

Status:
Completed
Trial end date:
2017-10-25
Target enrollment:
Participant gender:
Summary
Study WCMC IST-CTI-MDS evaluates the safety and tolerability of tosedostat in adult patients with pathologically confirmed MDS (< 20% blasts in bone marrow, peripheral blood, or both) by World Health Organization (WHO) classification after failure of hypomethylating agent-based therapy.
Phase:
Phase 2
Details
Lead Sponsor:
Weill Medical College of Cornell University
Collaborator:
CTI BioPharma
Treatments:
Glycine
Tosedostat