drugset / Trial / NCT00419250

A Dose Escalation Study of Lenalidomide in Relapsed or Refractory B-cell Chronic Lymphocytic Leukemia

NCT00419250 ↗

Phase 1 Completed 52 enrolled Celgene Corporation
RandomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety of lenalidomide and to define the maximum tolerated escalation dose level (MTEDL) when administered by a stepwise dose-escalation schedule in subjects with relapsed or refractory B-cell CLL.

Timeline

Start
2006-12-01
Primary completion
2010-02-01
Completion
2010-06-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 5 mg —
Subject Lenalidomide Other / unclassified 10 mg —
Subject Lenalidomide Other / unclassified 15 mg —
Subject Lenalidomide Other / unclassified 20 mg —
Subject Lenalidomide Other / unclassified 25 mg —