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临床试验/EUCTR2004-001749-13-AT
EUCTR2004-001749-13-AT进行中(未招募)1 期

Randomized Phase II Study: Temozolomide (TMZ) Concomitant to Radiotherapy followed by sequential TMZ in Advanced NSCLC Patients with CNS Metastasis versus Radiotherapy alone

AESCA Pharma GesmbH0 个研究点目标入组 92 人开始时间: 2004年12月17日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
92

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

  • ·Prior histologic confirmation of NSCLC
  • ·Optional: NSCLC histologic confirmation of metastasis of NSCLC
  • ·Presence of bidimensionally measurable disease in the brain
  • ·No previous or current malignancies at other sites with the exception of adequately treated in situ carcinoma of the cervix or basal and squamous carcinoma of the skin.
  • ·Age: > 18 years
  • ·No evidence of progression at extracranial sites
  • ·Karnofsky Performance status ³ 60 %
  • ·ANC > 1.500/mm3 , platelets > 100.000/mm3, hemoglobin > 8g/dl
  • ·Serum creatinine and bilirubine < 1.5 times upper normal limit of testing laboratory
  • ·SGOT; SGPT < 3 times upper limit of testing laboratory
  • ·Palliative radiation therapy to thorax and bone or other organs (except brain) is acceptable.
  • ·Prior neurosurgery > 2 weeks from initiating treatment with TMZ
  • ·Cortisone medication stable or decreasing within 2 weeks prior to initiating treatment with TMZ
  • ·Patient is not pregnant or nursing and is advised and willing to use an effective method of contraception
  • ·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

  • ·Chemotherapy or biologic therapy within four weeks prior initiating therapy with TMZ
  • ·Prior radiation therapy for brain < 4 weeks from initiating therapy with TMZ
  • ·Surgery within two weeks prior to TMZ administration
  • ·Known HIV disease
  • ·Acute infection requiring intravenous antibiotics
  • ·Rapid disease progression outside of brain at study entrance.
  • ·Any reason making compliance to the protocol improbable

研究者

发起方
AESCA Pharma GesmbH

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