drugset / Trial / NCT00511238

Phase 2 Study of Carfilzomib in Relapsed and Refractory Multiple Myeloma

NCT00511238

Phase 2 Completed 312 enrolled Amgen
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To evaluate the overall response rate and safety and tolerability of carfilzomib in subjects with relapsed and refractory multiple myeloma. Patients must have received prior treatment with bortezomib and either thalidomide or lenalidomide and be refractory to their last treatment.

Timeline

Start
2007-08
Primary completion
2010-11
Completion
2012-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Carfilzomib Other / unclassified 20 mg/m2 Intravenous
Subject Carfilzomib Other / unclassified 27 mg/m2 Intravenous

Indications