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Study of LBH589, A Deacetylase Inhibitor in Patients With Recurrent or Refractory Hodgkin or Non-Hodgkin's Lymphoma

2017年1月11日 更新者:Roswell Park Cancer Institute

Phase I Study of LBH589, A Novel Oral Deacetylase Inhibitor in Patients With Recurrent or Refractory Hodgkin or Non-Hodgkin's Lymphoma

The purpose of this study is to find out the effects of a drug called LBH589 when given to people with recurrent or refractory Hodgkin or Non-Hodgkin's lymphoma. The safety of this drug will also be studied. The participants' physical state, changes in the size of the tumor, or state of Hodgkin or non-Hodgkin's Lymphoma, and laboratory findings taken while on-study will help the researchers decide if LBH589 is safe and effective.

研究概览

详细说明

This is an open-label, standard 3-3 dose finding scheme with a modification that allows intra-patient dose modification to determine maximum tolerated dose and toxicity profile of LBH589 in patients with recurrent or refractory Hodgkin's or non-Hodgkin's lymphoma.

研究类型

介入性

注册 (实际的)

8

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • New York
      • Buffalo、New York、美国、14263
        • Roswell Park Cancer Institute

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Male or female patients age ≥ 18 years old with relapsed/refractory Hodgkin lymphoma or NHL patients who have relapsed or are refractory after receiving a minimum of two prior therapies
  • Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed

Laboratory requirements:

  • ANC ≥ 1.5 x 10(9th)/L, unless due to bone marrow involvement with lymphoma
  • Hemoglobin ≥ 9 g/dl without packed red blood cell dependency, unless due to bone marrow involvement with lymphoma
  • Platelets ≥ 100 x 10(9th)/L, unless due to bone marrow involvement with lymphoma
  • Serum creatinine ≤ 1.5 x Upper limit of Normal, or calculated Creatinine Clearance ≥ 50 mL/min
  • AST and ALT ≤ 2.5 x Upper limit of Normal, unless due to liver involvement with lymphoma
  • Serum bilirubin ≤ 1.5 x Upper limit of Normal
  • Albumin > 3.0 g/dl
  • Serum potassium ≥ Lower limit of Normal
  • Total serum calcium [corrected for serum albumin] or ionized calcium ≥ Lower limits of normal
  • Serum magnesium ≥ Lower limit of Normal
  • Serum phosphorus ≥ Lower limit of Normal
  • TSH ≥ LLN and free T4 within normal limits. Patients are permitted to receive thyroid hormone supplements to treat underlying hypothyroidism.
  • Baseline MUGA or ECHO must demonstrate LVEF ≥ 50%
  • ECOG Performance Status of ≤ 2

Exclusion Criteria:

  • Prior HDAC, DAC, HSP90 inhibitors or valproic acid for the treatment of cancer
  • Patients who will need valproic acid for any medication during the study or within 5 days prior to first LBH589 treatment
  • Peripheral neuropathy ≥ CTCAE grade 1
  • Impaired cardiac function or clinically significant cardiac diseases, including any one of the following:
  • Patients with congenital QT syndrome
  • History or presence of sustained ventricular tachyarrhythmia.
  • Any history of ventricular fibrillation or torsade de pointes
  • Bradycardia defined as Heart Rate < 50 bpm. Patients with pacemakers are eligible if Heart Rate ≥ 50 bpm
  • Screening EKG with a QTc.450msec
  • Right Bundle branch block + left anterior hemiblock (bifascicular block)
  • Patients with myocardial infarction or unstable angina ≤ 6 months prior to starting study drug
  • other clinically significant heart disease (e.g. CHF NY Heart Association class III or IV, uncontrolled hypertension, history of labile hypertension or history of poor compliance with an antihypertensive regimen)
  • Impairment of GI function or GI disease that may significantly alter the absorption of LBH589
  • Patients with Diarrhea > CTCAE grade 1
  • Other concurrent severe and/or uncontrolled medical conditions (e.g. uncontrolled diabetes or active or uncontrolled infection) including abnormal laboratory values that could cause unaccepted safety risks or compromise compliance with the protocol
  • Patients using medications that have a relative risk of prolonging the QT interval or inducing torsade de pointes if treatment cannot be discontinued or switched to a different medication prior to starting study drug
  • Concomitant use of CYP3A4 inhibitors
  • Patients who have received targeted agents within 2 weeks or within 5 half-lives of the agent and active metabolites(which ever is longer) and who have not recovered from side effects of those therapies
  • Patients who have received either immunotherapy within ≤ 8 weeks;chemotherapy within ≤ 4 weeks or radiation therapy to >30% of marrow-bearing bone within ≤ weeks prior to starting study treatment or who have not yet recovered from side effects of such therapies
  • Patients with an active bleeding tendency or is receiving any treatment with therapeutic doses of sodium warfarin or coumadin derivatives. Low doses of Coumadin (e.g.≤2 mg/day) to maintain line patency is allowed.
  • Patients who have undergone major surgery ≤ 4 weeks prior to starting study drug or who have not recovered from side effects of such therapy
  • Women who are pregnant or breast feeding or women of childbearing potential not using effective method of birth control
  • Male patients whose sexual partners are women of childbearing potential not using effective birth control
  • Patients with prior malignancy within 5 years (except for basal or squamous cell carcinoma, in situ cancer of the cervix or early stage prostate or bladder carcinomas)
  • Patients with known positivity for HIV or hepatitis C: baseline testing for HIV and Hepatitis C is not required
  • Prior allogenic stem cell transplant
  • Patients with any significant history of non-compliance to medical regimens or unwilling or unable to comply with the instructions given to him/her by the study staff
  • Patients taking CYP2D6 inhibitors should be carefully monitored, but these drugs are not necessarily contraindicated when use concomitantly with LBH. Use of these drugs is not an exclusion criterion

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:LBH589
LBH589 administered orally as once daily dose of 20 mg po q M, W, F on a q 28 day cycle, escalating to a maximum dase of 60 mg
LBH589 will be administered orally as once daily dose of 20 mg po q M, W, F on a q28 day cycle.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Determine maximum tolerated dose (MTD) of LBH589
大体时间:2 years
2 years

次要结果测量

结果测量
大体时间
Determine toxicity profile in study population
大体时间:28 days after Cycle 2 Day 1
28 days after Cycle 2 Day 1
Determine anti-lymphoma activity of LBH589 in (non-CTCL) Hodgkin's and non-Hodgkin's lymphoma patients
大体时间:2 Years
2 Years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

合作者

调查人员

  • 首席研究员:Francisco Hernandez, MD、Roswell Park Cancer Institute

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2009年12月1日

初级完成 (实际的)

2017年1月1日

研究完成 (实际的)

2017年1月1日

研究注册日期

首次提交

2009年12月14日

首先提交符合 QC 标准的

2009年12月14日

首次发布 (估计)

2009年12月15日

研究记录更新

最后更新发布 (估计)

2017年1月12日

上次提交的符合 QC 标准的更新

2017年1月11日

最后验证

2017年1月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

LBH589的临床试验

3
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