drugset / Trial / NCT01169636

Panobinostat Plus Ifosfamide, Carboplatin, and Etoposide (ICE) Compared With ICE For Relapsed Hodgkin Lymphoma

NCT01169636

Phase 1/2 Completed 62 enrolled M.D. Anderson Cancer Center Novartis · collab
RandomizedSingle-groupOpen-labelTreatment

Summary

Objectives: Primary objective: * Phase-I: To determine the maximal tolerated dose (MTD) of panobinostat (LBH589) + Ifosfamide + Mesna, Carboplatin and Etoposide (ICE) combination * Randomized Phase-II: To estimate the complete response (CR) rate in patients with relapsed and refractory classical Hodgkins Lymphoma (HL) receiving ICE versus PANOBINOSTAT plus ICE therapy Secondary Objectives: * To assess the safety and tolerability of the novel combination of PANOBINOSTAT (LBH589) plus ICE versus ICE in patients with relapsed and refractory HL * To estimate the overall response rate (CR + partial response PR) * To estimate the success rate of stem cell collection in patients eligible for stem cell transplant * To estimate the percentage of patients who subsequently undergo autologous stem cell transplantation (ASCT) * To estimate the event free survival (EFS) at 1 year after randomization * To determine pretreatment expression level of histone deacetylases (HDAC1), HDAC2, and pSTAT3 and Signal transducer and activator of transcription protein (pSTAT6) by Immunohistochemistry (IHC) and correlate the results with treatment response

Timeline

Start
2011-01-31
Primary completion
2017-05-17
Completion
2017-05-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Panobinostat Small molecule 20 mg Oral
Background 2-MERCAPTOETHANESULFONIC ACID Small molecule 2 g Intravenous
Background Carboplatin Small molecule Intravenous
Background Etoposide Small molecule 100 mg/m2 Intravenous
Background Ifosfamide Small molecule 5 g Intravenous
Background Pegfilgrastim Protein / enzyme biologic 6 mg Subcutaneous

Indications