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临床试验/EUCTR2005-005187-90-SE
EUCTR2005-005187-90-SE进行中(未招募)不适用

A Multicentre, Randomized Phase III Study of Rituximab as Maintenance Treatment versus Observation alone in Patients with Aggressive B-cell lymphoma:NHL-13 - NHL-13 (ML18223)

AGMT: Arbeitsgemeinschaft Medikamentöse Tumortherapie0 个研究点目标入组 600 人开始时间: 2006年10月17日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients must have received eight infusions of rituximab plus 4 – 8 cycles of CHOP-like chemotherapy including an anthracycline
  • Induction treatment must have been completed with the application of the final cycle of chemotherapy or immunotherapy no longer than 12 weeks, and no earlier than 4 weeks before trial treatment start.
  • Patients must have reached a complete remission (CR) or an unconfirmed CR (CRu) after induction therapy
  • Histologic diagnosis of either diffuse large B-cell lymphoma (DLBCL) or follicular lymphoma grade 3b according to the WHO/REAL classification at time of diagnosis (prior to induction therapy)
  • Confirmed CD20 positivity of the lymphoma at time of diagnosis (prior to induction therapy)
  • ECOG performance status of 0, 1 or 2 at time of inclusion (see Appendix IV )
  • Known IPI at time of diagnosis (prior to induction therapy)
  • Age 18 years or older
  • Life expectancy of at least 3 months
  • Be willing and able to comply with the protocol for the duration of the study
  • Women of child-bearing potential must have a negative pregnancy test and must agree to use effective contraception for the entire treatment period and during the 12 months thereafter.
  • Patient’s written informed consent
  • 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

排除标准

  • First-line NHL therapy other than specified in the inclusion criteria
  • More than one prior chemoimmunotherapy regimen.
  • Histologies other than DLBCL and follicular lymphoma grade 3b according to the WHO/REAL classification
  • Transfomed lymphoma
  • History of malignancy other than squamous cell carcinoma, basal cell carcinoma of the skin, surgically treated malignant melanoma or carcinoma in situ of the cervix within the last 5 years.
  • Major surgery, other than diagnostic surgery, within the last 4 weeks.
  • Evidence of CNS involvement. Patients with a history of uncontrolled seizures, central nervous system disorders or psychiatric disability judged by the Investigator to be clinically significant and adversely affecting compliance to study drugs.
  • Clinically significant cardiac disease (e.g. congestive heart failure, symptomatic coronary artery disease and cardiac arrhythmias not well controlled with medication) or myocardial infarction within the last 6 months.
  • Unacceptable hematologic status at baseline prior to study start below any of the values listed: WBC: <3 x 109/L; absolute neutrophil count (segmented + bands) <1.5 x 109/L; platelets: <100 x109/L
  • Abnormal liver function tests prior to study start above any of the values listed: serum bilirubin >2 mg/dL (35 mmol/L); ALAT or ASAT >2.5 x upper limit of normal range; alkaline phosphatase > 3 x upper limit of normal range
  • Abnormal renal function (serum creatinine > 2.0 mg/dL (177 µmol/L)).
  • Patients with active opportunistic infections.
  • HIV-positive patients.
  • Life expectancy of less than 3 month.

研究者

发起方
AGMT: Arbeitsgemeinschaft Medikamentöse Tumortherapie

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