An International, Multicenter, Randomized, Double-Blind Study of Vorinostat (MK-0683) or Placebo in Combination with Bortezomib in Patients with Multiple Myeloma

Merck & Co., Inc0 个研究点目标入组 742 人开始时间: 2009年11月5日最近更新: 2015年8月4日

适应症

试验速览

暂无简介。

•1. Patient has an established diagnosis of multiple myeloma based on the myeloma diagnostic criteria.
•2. Patient has received at least 1 but not more than 3 prior anti-myeloma regimens and has progressive disease after the most recent treatment regimen as per the European Blood and Marrow Transplantation Group (EBMT) Criteria.
•3. Patient who received prior bortezomib-containing regimen and meets the following criteria is also eligible: While on prior bortezomib-based therapy, the patient must have achieved a minimal response (MR), partial response (PR), or complete response (CR). Patient was not considered bortezomib refractory.
•4. Patient has measurable disease, defined as any quantifiable serum M-protein value and, where applicable, urine light chain of =200 mg/24 hours.
•5. Patient has adequate organ function.
•A full list of criteria can be found in the protocol.
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range

•1. Patient has had any prior allogeneic bone marrow transplant (patient with prior autologous transplant are eligible).
•2. Patient plans to undergo any type of bone marrow transplantation (allogeneic, or autologous) within 4 weeks after initiating study therapy.
•3. Patient has had prior treatment with vorinostat or HDAC inhibitors (e.g., depsipeptide, MS-275, LAQ-824, PXD-101, LBH589, MGCD0103, CRA024781, etc.). Patients who have received compounds with HDAC inhibitor-like activity, such as valproic acid, as anti-tumor therapy should not be enrolled in this study. (Patients who have received such compounds for other indications, e.g. valproic acid for epilepsy, may enroll after a 30-day washout period.)
•4. Patient is receiving corticosteroid therapy (>10 mg of prednisone or equivalent). However, use of =10 mg of prednisone or equivalent is allowed for reasons other than myeloma.
•A full list of criteria can be found in the protocol.

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