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临床试验/jRCT2031230036
jRCT2031230036已完成不适用

Anti-PD-1 antibody therapy for epithelial skin malignancies: an investigator-initiated, open-label, single-arm, multicenter, expanded access program.

未提供0 个研究点目标入组 27 人开始时间: 2023年4月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
27
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • •Age 20 years or older
  • •Patients who are incurable by surgical treatment and radiation treatment, and who have been confirmed by histology to have advanced or recurrent epithelial skin malignancies
  • •Patients who have more than one of measurable lesions or immeasurable lesion as defined in RECIST Guideline Version 1.1 within 14 days prior to enrollment in this clinical trial
  • •Patients with ECOG PS 0-1

排除标准

  • •Patients who have high degree of hypersensitivity or medical history of the other antibody product
  • •Patients who judged by principal investigator or sub-investigator to influence the drug safety evaluation, because of who have been remained side effects of previous treatment or the impact of the surgery
  • •Patients who have been merged the autoimmune disease or who have medical history of the autoimmune disease (chronic or recurrent)
  • •Patients who have cancer duplication (However, patients who have been completely resected carcinoma (basal cell, epithelial, mucosal or superficial bladder) or patients who have other carcinoma that don't show recurrence more than five years before obtaining consent are can be registered)
  • •Patients who have central nervous system metastasis (However, patients who are asymptomatic and do not need treatment can be registered)

结局指标

主要结局

-

Type, frequency and severity of adverse events(CTCAE ver. 5.0)

次要结局

未报告次要终点

研究者

发起方
未提供

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