drugset / Trial / NCT00981708

Lenalidomide, Dexamethasone and Cyclophosphamide in Amyloidosis (AL)

NCT00981708

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety and activity of the combination of lenalidomide with intermediate dose dexamethasone and cyclophosphamide in patients with primary systemic (AL ) amyloidosis.

Timeline

Start
2008-02
Primary completion
2011-01-11
Completion
2016-01-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 50 mg Oral
Subject Cyclophosphamide Other / unclassified 100 mg Oral
Subject Dexamethasone Small molecule 20 mg Oral
Subject Lenalidomide Other / unclassified 5 mg Oral
Subject Lenalidomide Other / unclassified 15 mg Oral
Subject Lenalidomide Other / unclassified 25 mg Oral

Indications