Overview

Phase 1 Study of Terameprocol (EM-1421) in Patients With Leukemia

Status:
Terminated
Trial end date:
2009-06-01
Target enrollment:
Participant gender:
Summary
This study is designed to determine the safety, maximum tolerated dose,dose limiting toxicity of Terameprocol(EM-1421)and determine the pharmacokinetics (clearance from the blood)of Terameprocol(EM-1421)given as intravenous infusion three times a week in patients with leukemia.
Phase:
Phase 1
Details
Lead Sponsor:
Erimos Pharmaceuticals
Treatments:
Masoprocol