CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 767 enrolled
Drug / intervention
Panobinostat +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01023308
NCT01023308Phase 3Completed

A Multicenter, Randomized, Double Blind, Placebo Controlled Phase III Study of Panobinostat in Combination With Bortezomib and Dexamethasone in Patients With Relapsed Multiple Myeloma

Novartis Pharmaceuticals·interventional·Posted Dec 2, 2009·Updated Mar 17, 2020

In Brief

A Phase 3 clinical trial evaluating Panobinostat, Bortezomib, and 2 other interventions for Multiple Myeloma. Completed, enrolled 767 participants across 210 sites in 34 countries.

Detailed Summary

Panobinostat (LBH589) is a highly potent pan-deacetylase inhibitor (pan-DACi), inclusive of HDAC6, which disrupts aggresome function, promotes accumulation of cytotoxic misfolded protein aggregates and triggers myeloma cell death. Combination of pan-DAC and protease inhibition by co-treatment with panobinostat (PAN) and bortezomib (BTZ) has demonstrated synergistic cytotoxicity in vitro and in vivo in pre-clinical experiments. Furthermore, clinical experience in advanced multiple myeloma (MM) patients treated by oral panobinostat and i.v bortezomib ± dexamethasone showed very encouraging results for efficacy and manageable toxicity profile. Given the medical need for improved treatment strategies for patients with previously treated and relapsed MM, the purpose of this prospective, multinational, randomized, double-blind, placebo-controlled, parallel group Phase III study is to compare the results in progression-free survival of 2 combination therapies, panobinostat with bortezomib and dexamethasone or placebo with bortezomib and dexamethasone, in patients with previously treated MM whose disease has recurred or progressed.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Australia, Austria, Belgium, Brazil, Canada, China, Czechia, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Israel, Italy, Japan, Lebanon, Mexico, Netherlands, Norway, Poland, Russia, Singapore, South Africa, South Korea, Spain, Sweden, Taiwan, Thailand, Turkey (Türkiye), United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedDec 2, 2009
Enrollment StartDec 21, 2009
Primary CompletionJul 30, 2015
TodayJul 2, 2026
Enrollment to primary: 5.6 yearsPosted 16.6 years ago

Interventions

Panobinostatdrug

Panobinostat was administered 3x week ( 2 weeks on 1 week off)

Bortezomibdrug

Bortezomib was administered 2 x week ( 2weeks on 1 week off)

Dexamethasonedrug

Dexamethasone was adminstered on day of Bortezomib and the day after Bortezomib administration

Placebodrug

Placebo was administered 3x week ( 2 weeks on 1 week off)