drugset / Trial / NCT01686386

Study of Bendamustine, Lenalidomide and Low-dose Dexamethasone, for the Treatment of Patients With Relapsed Myeloma

NCT01686386

Phase 1/2 Unknown 60 enrolled Gruppo Italiano Studio Linfomi
NaSingle-groupOpen-labelTreatment

Summary

This is an open Label, Phase I/II, multicenter study. In the first phase it defines the maximum tolerated dose (MTD) of Bendamustine (B) given in combination with Lenalidomide (L) and low-dose Dexamethasone (d) and in the second phase it evaluates the antitumour activity of Bendamustine, Lenalidomide and Low-dose Dexamethasone (BdL) given in combination, in relapsed multiple myeloma patients.

Timeline

Start
2010-02
Primary completion
2012-04
Completion
2013-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bendamustine Small molecule 40 mg/m2
Subject Lenalidomide Other / unclassified 10 mg
Background Dexamethasone Small molecule 40 mg

Indications