drugset / Trial / NCT00126893

Study to Determine the Optimal Biologic Dose of CC-401 in Subjects With High-Risk Myeloid Leukemia

NCT00126893 ↗

Phase 1 Terminated 36 enrolled Celgene Corporation
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a single center Phase 1 study to evaluate the safety, pharmacokinetics and pharmacodynamics of CC-401 in subjects with refractory acute myelogenous leukemia.

Timeline

Start
2005-10
Primary completion
—
Completion
2006-09

Drugs

EvaluationDrugModalityDoseRoute
Subject CC-401 Small molecule — —

Indications