drugset / Trial / NCT02128230

UARK 2012-02 Trial For High-Risk Myeloma Evaluating Accelerating and Sustaining Complete Remission

NCT02128230

Phase 2 Terminated 20 enrolled University of Arkansas Amgen · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to improve the clinical outcomes of research subjects with high-risk multiple myeloma in the context of the immediately preceding Total therapy 5 trial 2008-02 and Total therapy 3 trials 2003-33 and 2006-66.

Timeline

Start
2014-06-10
Primary completion
2019-02-19
Completion
2019-02-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Carfilzomib Other / unclassified 20 mg/m2 Intravenous
Subject Carfilzomib Other / unclassified 27 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 7.5 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 10 mg/m2 Intravenous
Subject Cyclophosphamide Other / unclassified 75 mg/m2 Intravenous
Subject Cyclophosphamide Other / unclassified 100 mg/m2 Intravenous
Subject Cyclophosphamide Other / unclassified 300 mg/m2 Intravenous
Subject Cyclophosphamide Other / unclassified 400 mg/m2 Intravenous
Subject Dexamethasone Small molecule 12 mg Oral
Subject Dexamethasone Small molecule 20 mg Oral
Subject Dexamethasone Small molecule 40 mg Oral
Subject Doxorubicin Other / unclassified 7.5 mg/m2 Intravenous
Subject Doxorubicin Other / unclassified 10 mg/m2 Intravenous
Subject Etoposide Small molecule 30 mg/m2 Intravenous
Subject Etoposide Small molecule 40 mg/m2 Intravenous
Subject Etoposide Small molecule 60 mg/m2 Intravenous
Subject Etoposide Small molecule 80 mg/m2 Intravenous
Subject Melphalan Small molecule 5 mg/m2 Intravenous
Subject Melphalan Small molecule 10 mg/m2 Intravenous
Subject Melphalan Small molecule 20 mg/m2 Intravenous
Subject Thalidomide Other / unclassified 50 mg Oral
Subject Thalidomide Other / unclassified 100 mg Oral
Subject Thalidomide Other / unclassified 200 mg Oral
Background filgrastim Protein / enzyme biologic 10 ug/kg Subcutaneous

Indications