NCT01632826Approved For Marketing不适用
A Multicenter, Single-Arm, Open-Label Treatment Use Protocol for Pomalidomide (POM) in Combination With Low Dose Dexamethasone (LD-Dex) in Patients With Relapsed or Refractory Multiple Myeloma
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- Approved For Marketing
- 发起方
- Celgene
- 试验地点
- 1
研究概览
简要总结
To provide pomalidomide access to relapsed/refractory multiple myeloma subjects with a likelihood of benefit from the pomalidomide treatment while the medication is not commercially available
详细描述
Several clinical studies indicate that pomalidomide has activity in relapsed and refractory multiple myeloma with response rates ranging between 30% and 60% at pomalidomide doses at 2 mg/day and/or 4 mg/day.
研究设计
- 研究类型
- Expanded Access
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Must have documented diagnosis of relapsed or relapsed/refractory multiple myeloma and have measurable disease (serum or urine M-protein)
- •Age ≥ 18 years
- •Must have had at least ≥ 2 prior anti-myeloma therapies
- •Must have received at least 2 consecutive cycles of both lenalidomide and bortezomib, either alone or in combination
- •Must have failed treatment with the last lenalidomide-containing regimen and the last bortezomib-containing regimen
- •Must have documented disease progression during or after the last antimyeloma regimen
- •Females of childbearing potential (FCBP) must agree to utilize two reliable forms of contraception simultaneously or practice complete abstinence from heterosexual contact for at least 28 days before starting drug, while participating in the study and for at least 28 days after study treatment discontinuation.
- •Males must agree to use a latex condom during sexual contact with FCBP while participating in the study and for 28 days following discontinuation from study treatment.
排除标准
- •Peripheral Neuropathy ≥ Grade 2
- •Non-secretory multiple myeloma
- •Previous therapy with pomalidomide
- •Use of any investigational agents within 28 days or 5 half lives (whichever is longer) of initiating study treatment
- •Subjects with conditions requiring chronic steroid or immunosuppressive treatment.
- •Hypersensitivity to thalidomide, lenalidomide or dexamethasone
- •Known Human Immunodeficiency Virus positive, active or chronic Hepatitis A, B or C
- •Pregnant or breastfeeding females
- •Unacceptable hematological or biochemical laboratory abnormalities
研究者
研究点 (1)
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