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再発性多発性骨髄腫患者におけるパノビノスタットまたはプラセボとボルテゾミブおよびデキサメタゾンの併用療法

基本情報

NCT ID
NCT01023308
ステータス
完了
試験のフェーズ
第3相
試験タイプ
介入
目標被験者数
767
治験依頼者名
Novartis

概要

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.

対象疾患

Multiple Myeloma

介入

Panobinostat(DRUG)
Bortezomib(DRUG)
Dexamethasone(DRUG)
Placebo(DRUG)

依頼者(Sponsor)