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临床试验/NCT02943473
NCT02943473终止2 期

A Phase 2 Study of the Effect of the Bruton's Tyrosine Kinase Inhibitor Ibrutinib on Disease Response in Patients With High Risk Smoldering Multiple Myeloma

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2017年5月18日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
终止
入组人数
9
试验地点
1
主要终点
Number of Patients Without Symptomatic Myeloma

研究概览

简要总结

The purpose of this research study is to test whether the drug ibrutinib (trademark name: IMBRUVICA®) is effective at preventing the development of multiple myeloma in people who currently have smoldering myeloma. The researchers conducting this trial) have reason to believe that ibrutinib can delay the development of multiple myeloma, thus giving people who currently have smoldering myeloma a longer period of time when they feel healthy and well.

Smoldering myeloma is an abnormal condition that is considered to be an early phase of the disease multiple myeloma. In this disorder, there is an abnormal growth of plasma cells, which is a type of blood cell found in the bone marrow. This growth is not as severe in people with smoldering myeloma as it is in multiple myeloma, so people with smoldering myeloma do not have any symptoms and tend to feel well. However, they have a higher risk of developing multiple myeloma than people in the general population.

Some people with smoldering myeloma are at an especially high risk of developing myeloma - 50% of these people will develop multiple myeloma 2 years after they are diagnosed with smoldering myeloma. The investigators identify these people by looking at the amount of myeloma in the bone marrow (called "bone marrow plasma cell percentage") and the amount of myeloma protein (called "serum protein electrophoresis" and "serum free light chain assay") in the blood. To be considered high risk, individuals must have highly abnormal levels for these tests.

Based upon current guidelines, people with smoldering myeloma do not require any treatment. However, known is that many of these people will develop multiple myeloma in the near future. Currently there have been no proven and effective way of preventing these people from developing multiple myeloma, which remains an incurable disease.

详细描述

This is a phase 2, open-label, single center, prospective pilot study designed to assess the efficacy of ibrutinib in subjects with high risk smoldering multiple myeloma.

All enrolled subjects will be treated with ibrutinib 560 mg (4 capsules, each containing 140 mg) taken PO daily for 12 cycles (28 days each). If a subject demonstrates benefit from ibrutinib, therapy may be extended beyond 12 cycles to a maximum of 2 years. Subjects who progress and meet criteria for symptomatic multiple myeloma will be withdrawn from study.

An initial cohort of 15 subjects will be accrued. If 4 or more patients progress to symptomatic myeloma in one year, then the study will be reviewed with the FDA to determine whether to employ a higher dose of ibrutinib, or to stop for futility. Otherwise, 21 additional patients will be accrued for a total sample size of 36.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Ibrutinib

Experimental

Ibrutinib (trademark name is IMBRUVICA®). 560 mg dose administered on a continuous basis

干预措施: Ibrutinib (Drug)

结局指标

主要结局

Number of Patients Without Symptomatic Myeloma

时间窗: up to 1 year

Disease response - the proportion of patients with high risk smoldering multiple myeloma who do not progress to symptomatic myeloma as defined by the IMWG.

次要结局

  • Change in Serum Interleukin-6 (IL-6)(baseline and up to one year)
  • Change in Serum Macrophage Inflammatory Protein-1α (MIP-1α)(baseline and up to one year)
  • Change in Serum C-terminal Telopeptide (CTX)(baseline and up to one year)
  • Bone Density Changes(baseline and one year)
  • PET-MRI Changes(baseline and one year)
  • Change in Serum Stromal Cell-derived Factor-1 (SDF-1)(baseline and up to one year)
  • Change in Serum Dickkopf-1 (DKK-1)(baseline and up to one year)
  • Overall Response Rate(up to 1 year)
  • Change in Serum Receptor Activator of Nuclear-factor Kappa B Ligand (RANKL)(baseline and up to one year)
  • Change in Urine N-terminal Telopeptide (NTx)(baseline and up to one year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ajai Chari

Associate Professor

Icahn School of Medicine at Mount Sinai

研究点 (1)

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