NL-OMON52284招募中不适用
A clinical imaging Study of the changes in [18F]F-AraG uptake following radiotherapy in Non-small cell lung cancer. - SHARP
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 12
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Histologically confirmed NSCLC, melanoma, esophageal, or breast cancer
- •Ongoing immunotherapy using an anti-PD-(L)1 agent
- •Planned to be treated with high dose (24Gy) radiotherapy per clinical
- •Be willing and able to provide written informed consent for the trial.
- •Have a performance status of 0-2 on the ECOG Performance Scale
- •Be above 18 years of age on day of signing informed consent.
排除标准
- •Subjects with a condition requiring systemic treatment with either
- •corticosteroids (>10 mg daily prednisone equivalent) or other immunosuppressive
- •medications within 14 days of day 0. Inhaled or topical steroids, and adrenal
- •replacement steroid >10 mg daily prednisone equivalent, are permitted in the
- •absence of active autoimmune disease.
- •Psychiatric or substance abuse disorders that would interfere with
- •cooperation with the requirements of the trial.
- •Patient is pregnant or breastfeeding, or expecting to conceive within the
- •projected duration of the trial, starting with the screening visit through 12
- •weeks after the last administration of [18F]F-AraG.
研究者
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