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临床试验/NCT05464823
NCT05464823进行中(未招募)不适用

Feasibility of Combined Genomics/Transcriptomics for Patients With Lymphoma

M.D. Anderson Cancer Center1 个研究点 分布在 1 个国家目标入组 111 人开始时间: 2022年7月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
111
试验地点
1
主要终点
Percentage of participants who have genomic test results available in <=7 days

研究概览

简要总结

To learn more about the usefulness of molecular testing with the Molecular Functional (MF) Portrait (a commercial test conducted by the sponsor of this study, BostonGene) in guiding lymphoma care.

详细描述

Primary Objective:

• To determine the feasibility and turnaround of clinical WES and transcriptome sequencing

Secondary Objectives:

  • To determine the frequency of actionable DNA and RNA alterations
  • To determine the concordance of DNA and RNA alterations
  • To determine the frequency of molecularly matched therapy
  • To determine the feasibility of identifying mechanism(s) of acquired resistance with genomic profiling
  • To determine the feasibility of molecularly matched therapy to acquired resistance alterations

Exploratory Objectives:

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

  • Patient Eligibility:
  • Inclusion Criteria:
  • Male/female patients who are at least 18 years of age on the day of informed consent signing.
  • Patients must have a histologically documented diffuse large B-cell lymphoma requiring therapy.
  • Provision of written informed consent for the study.

排除标准

  • 未提供

研究组 & 干预措施

Molecular Testing

Other

Molecular Functional (MF) Portrait (a commercial test conducted by the sponsor of this study, BostonGene) in guiding lymphoma care.

干预措施: Molecular Functional Portrait (Other)

结局指标

主要结局

Percentage of participants who have genomic test results available in <=7 days

时间窗: through study completion an average of 1 year

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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