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临床试验/NCT07390617
NCT07390617招募中不适用

Interrogating Enfortumab Vedotin-associated Neuropathy in Patients With Metastatic or Muscle-Invasive Urothelial Carcinoma Receiving Enfortumab Vedotin

Memorial Sloan Kettering Cancer Center7 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年1月20日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
7
主要终点
Change in Nerve Conduction Studies/NCS from baseline to 12-15 weeks

研究概览

简要总结

The purpose of this study is to see how results of nerve tests change in people with urothelial cancer who receive treatment with enfortumab vedotin (EV)

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Written informed consent by and HIPAA authorization for release of personal health information obtained from the research participant.
  • Able to speak and read English to a sufficient level of fluency to provide informed consent and complete the study questionnaires.
  • Age ≥ 18 years at the time of consent.
  • ECOG Performance Status of ≤ 3 within 28 days prior to consent.
  • Histological or cytologically confirmed urothelial carcinoma.
  • Patients must be planned to start systemic therapy with enfortumab vedotin
  • At time of enrollment, patients must be planned to start enfortumab with or without pembrolizumab

排除标准

  • Subjects meeting any of the criteria below may not participate in the study:
  • Inability of the subject to understand and comply with study procedures.
  • Having previously received enfortumab vedotin
  • Students/employees of the study institution, pregnant women, prisoners, and institutionalized individuals (to prevent enrollment of vulnerable subjects).

研究组 & 干预措施

Participants With Urothelial Carcinoma

Participants will have histological or cytologically confirmed urothelial carcinoma

干预措施: Non-therapeutic Nerve Conduction Studies (Other)

Participants With Urothelial Carcinoma

Participants will have histological or cytologically confirmed urothelial carcinoma

干预措施: Non-therapeutic assessment of patient-reported neuropathy (Other)

结局指标

主要结局

Change in Nerve Conduction Studies/NCS from baseline to 12-15 weeks

时间窗: up to 4 months

Describe change in Nerve Conduction Studies/NCS from baseline to 12-15 weeks. An NCS measures the flow of electrical current through motor and sensory nerves.

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 (7)

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