drugset / Trial / NCT02406222

Pomalidomide in Relapsed and Refractory Multiple Myeloma (RRMM)

NCT02406222

Phase 2 Active not recruiting 124 enrolled University of Leeds Celgene Corporation · collabMyeloma UK · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is determining whether the addition of cyclophosphamide to pomalidomide and dexamethasone improves progression free survival in patients with relapsed refractory myeloma (RRMM) compare to pomalidomide and dexamethasone alone. Patients will be randomised on a 1:1 basis to receive CPD or Pd. Treatment will be continued until disease progression or unacceptable toxicity.

Timeline

Start
2016-03
Primary completion
2022-12
Completion
2025-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 500 mg Oral
Subject Pomalidomide Other / unclassified 4 mg Oral
Background Dexamethasone Small molecule 40 mg Oral

Indications