drugset / Trial / NCT01368757

Lenalidomide in Patients With Chronic Myelomonocytic Leukemia

NCT01368757 ↗

NaSingle-groupOpen-labelTreatment

Summary

In a phase I study the investigators plan to investigate safety and toxicity of lenalidomide in patients with Chronic Myelomonocytic Leukemia (CMML). A phase II study will be started once an optimal dose has been found. The primary endpoint will concern the efficacy of lenalidomide in patients with CMML according to the WHO diagnostic criteria.

Timeline

Start
2010-06
Primary completion
2015-05
Completion
2015-05

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 —