跳至主要内容
临床试验/NCT07096999
NCT07096999招募中不适用

SPECT/CT Imaging for Dosimetry in 177Lu-PSMA-617 (Pluvicto) Therapy

University of Michigan Rogel Cancer Center1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年1月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
Response and toxicity following 177Lu-RLT

研究概览

简要总结

This study is being performed to establish the association between absorbed dose to tumor and response and absorbed dose to normal organs and toxicity following Lu177-PSMA radioligand therapy

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
Male
接受健康志愿者
否

入选标准

  • •* 177Lu-617 PSMA treatment scheduled for mCRPC
  • •Clinically stable as determined by the nuclear medicine clinicians
  • •≥ 18 years of age
  • •Willing and able to provide informed consent

排除标准

  • •Patients who are unable to lie flat on the imaging systems long enough to permit imaging protocols to be performed

研究组 & 干预措施

Observational

Patients receive standard care Pluvicto and undergo Lu-177 SPECT/CT scans on study. Patients may also undergo optional 99mTc-SC SPECT/CT scan for bone marrow dosimetry prior to cycle 1. In addition, patients have their medical records reviewed on study.

干预措施: Non-Interventional Study (Other)

结局指标

主要结局

Response and toxicity following 177Lu-RLT

时间窗: Up to 4 years

Association between absorbed dose and effect (response/toxicity) following 177Lu-RLT

次要结局

  • Build and test models(Up to 4 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验