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NCT01835561 Study to Evaluate Pharmacokinetics of Pomalidomide in Hepatically Impaired Males Status COMPLETED Phase PHASE1
NCT01807286 Pomalidomide With Melphalan and Dexamethasone for Untreated Systemic AL Amyloidosis Status TERMINATED Phase PHASE1
NCT01794039 Pomalidomide or Lenalidomide and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma Previously Treated With Lenalidomide Status COMPLETED Phase PHASE2
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NCT01745640 Pomalidomide and Dexamethasone Effects in Multiple Myeloma Patients With Del 17p or t (4;14) Status COMPLETED Phase PHASE2
NCT01745588 Autologous Stem Cell Transplant With Pomalidomide (CC-4047®) Maintenance Versus Continuous Clarithromycin/ Pomalidomide / Dexamethasone Salvage Therapy in Relapsed or Refractory Multiple Myeloma Status COMPLETED Phase PHASE2
NCT01734928 Safety and Efficacy of Pomalidomide, Bortezomib and Low-dose Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma Status COMPLETED Phase PHASE3
NCT01728259 First-line Pomalidomide, Bortezomib, and Dexamethasone For AL Amyloidosis or LCDD Status TERMINATED Phase PHASE1
NCT01722305 Pomalidomide and Dexamethasone in Treating Patients With Relapsed or Refractory Primary Central Nervous System Lymphoma or Newly Diagnosed or Relapsed or Refractory Intraocular Lymphoma Status COMPLETED Phase PHASE1
NCT01712789 Evaluation of Safety of Pomalidomide in Combination With Dexamethasone (Low Dose) in Patients With Refractory or Relapsed and Refractory Multiple Myeloma Status COMPLETED Phase PHASE3
NCT01707407 A Phase 1 Open-Label Study to Evaluate the Effect of CYP450 and P-gp Inhibition and Induction on the Pharmacokinetics of Pomalidomide (CC-4047) in Healthy Male Subjects Status COMPLETED Phase PHASE1
NCT01665794 Carfilzomib, Pomalidomide, and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma Status COMPLETED Phase PHASE1/PHASE2
NCT01632826 Pomalidomide (POM) in Combination With Low Dose Dexamethasone (LD-Dex) in Patients With Relapsed or Refractory Multiple Myeloma Status APPROVED_FOR_MARKETING Phase N/A