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临床试验/EUCTR2017-002063-17-IT
EUCTR2017-002063-17-IT进行中(未招募)1 期

A single arm phase II trial evaluating the activity of alectinib for the treatment of pretreated RET-rearranged advanced NSCLC - ALERT-lung: ALEctinib for the treatment of pre-treated RET-rearranged advanced non-small cell lung c

EUROPEAN THORACIC ONCOLOGY PLATFORM0 个研究点目标入组 44 人开始时间: 2021年5月24日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
44

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

  • - Histologically or cytologically-documented non-small cell lung
  • - Advanced disease defined as recurrent stage IV (according to 8th TNM
  • classification) or recurrent or progressive disease following multimodal
  • therapy (radiation therapy, surgical
  • resection, or definitive chemo-radiation therapy for locally advanced
  • - RET rearrangement detected by FISH, Nanostring or by parallelsequencing
  • on FFPE tumour tissue (biopsy, resection or cytoblock)
  • assessed locally.
  • - Availability of FFPE tumour material for central confirmation of RETrearrangement
  • - At least one prior platinum-based systemic regimen: Adjuvant or
  • neoadjuvant or definitive platinum-based chemo-radiotherapy
  • treatments are considered as a line of treatment only if completed lesthan 6 months before enrolment. Maintenance therapy following
  • platinum doublet-based chemotherapy is not considered a separate
  • regimen of therapy.
  • - Measurable or non-measurable, but radiologically evaluable (except for
  • skin lesions) disease according to RECIST v1.1 criteria
  • - Adequate haematological, renal and liver function
  • - ECOG Performance Status 0-2
  • 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 22
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 22

排除标准

  • - Untreated, active CNS metastases
  • - Carcinomatous meningitis
  • - Baseline symptomatic bradycardia
  • - Prior treatment with any RET TKI or RET targeted therapy
  • - Known EGFR, ALK, ROS, and BRAF mutation (in addition to RET
  • rearrangement)
  • - Any GI disorder that may affect absorption of oral medications, such as
  • malabsorption syndrome or status post-major bowel resection
  • - History of hypersensitivity to any of the additives in the alectinib drug
  • formulation
  • - Pregnant or lactating women
  • - Known HIV positivity or AIDS-related illness
  • - Any concurrent systemic anticancer therapy

研究者

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