drugset / Trial / NCT01217957

A Study of Ixazomib Administered in Combination With Lenalidomide and Low-Dose Dexamethasone in Patients With Newly Diagnosed Multiple Myeloma

NCT01217957

Phase 1/2 Completed 65 enrolled Millennium Pharmaceuticals, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of Phase 1 of this study was to determine the safety, tolerability, maximum tolerated dose (MTD), and recommended Phase 2 dose (RP2D) of oral ixazomib administered in combination with lenalidomide and low-dose dexamethasone in participants with newly diagnosed multiple myeloma (NDMM). The purpose of Phase 2 of this study was to determine the overall response rate (ORR) and further evaluate the tolerability and toxicity of the combination of oral ixazomib, lenalidomide, and low-dose dexamethasone in patients with NDMM.

Timeline

Start
2010-11-22
Primary completion
2013-03-08
Completion
2018-02-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Ixazomib Unknown 1.68 mg/m2 Oral
Subject Ixazomib Unknown 2.23 mg/m2 Oral
Subject Ixazomib Unknown 2.97 mg/m2 Oral
Subject Ixazomib Unknown 3.95 mg/m2 Oral
Subject Ixazomib Unknown 4 mg Oral
Background Dexamethasone Small molecule 40 mg Oral
Background Lenalidomide Other / unclassified 25 mg Oral

Indications