drugset / Trial / NCT01677858

A Study of Weekly Carfilzomib in Combination With Dexamethasone for Progressive Multiple Myeloma

NCT01677858

Phase 1/2 Completed 116 enrolled Amgen
NaSequentialOpen-labelTreatment

Summary

The study had the following primary objectives: * Phase 1: to determine the maximum tolerated dose (MTD) of once-weekly (QW) carfilzomib and dexamethasone for patients with relapsed or refractory multiple myeloma who have received 1 to 3 prior therapies * Phase 2: to estimate the overall response rate (ORR) for patients with relapsed or refractory multiple myeloma who received 1 to 3 prior therapies treated with carfilzomib and dexamethasone QW at the MTD established in phase 1.

Timeline

Start
2012-07-04
Primary completion
2016-07-22
Completion
2018-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Carfilzomib Other / unclassified 45 mg/m2 Intravenous
Subject Carfilzomib Other / unclassified 56 mg/m2 Intravenous
Subject Carfilzomib Other / unclassified 70 mg/m2 Intravenous
Subject Carfilzomib Other / unclassified 88 mg/m2 Intravenous
Background Dexamethasone Small molecule 40 mg Intravenous

Indications