drugset / Trial / NCT02756663

Panobinostat in Combination With Carfilzomib and Dexamethasone in Relapsed or Relapsed and Refractory Multiple Myeloma

NCT02756663

Phase 2 Withdrawn Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to investigate the anti-myeloma effect of panobinostat given at two different doses (10 mg and 20 mg oral) in combination with carfilzomib (20/56 mg/m2 i.v.) and low dose dexamethasone (20 mg oral) vs carfilzomib plus low-dose dexamethasone in patients with relapsed or relapsed and refractory multiple myeloma. Safety and efficacy will be evaluated. Treatment will be administered in 4-week cycles until patients discontinue due to disease progression or unacceptable toxicity or for other reasons. Patients who discontinue the study treatment for reasons other than documented disease progression will be followed for disease assessments every 8 weeks until progression. All patients will be followed for survival until 3 years have passed from their entry into the study, or they have discontinued the follow up earlier.

Timeline

Start
2016-12
Primary completion
2021-02
Completion
2021-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Panobinostat Small molecule 10 mg Oral
Subject Panobinostat Small molecule 20 mg Oral
Background Carfilzomib Other / unclassified 56 mg/m2 Intravenous
Background Dexamethasone Small molecule 20 mg Oral

Indications