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临床试验/jRCT2051220026
jRCT2051220026已完成不适用

Clinical Study of OP-07 for Delayed Methotrexate Elimination with Methotrexate-Leucovorin Rescue Therapy (OP-07-002 study)

Ohara Pharmaceutical Co., Ltd.0 个研究点目标入组 10 人开始时间: 2022年7月27日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
10
主要终点
Blood MTX concentration

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
No limit 至 No limit(—)
性别
All

入选标准

  • Patients whose written informed consent to participate in this study has been obtained from the patient or his/her legally authorized representative
  • Patients with delayed MTX elimination during MTX-LV rescue therapy. Delayed MTX elimination should be referred to the following blood MTX concentrations as a guide.
  • Time elapsed after administration of MTX (24 hours), with or without any signs of acute kidney injury; 50 micro mol/L
  • Time elapsed after administration of MTX (42 hours), without any signs of acute kidney injury; >= 5 micro mol/L
  • Time elapsed after administration of MTX (42 hours), with any sign of acute kidney injury; >= 1 micro mol/L
  • Time elapsed after administration of MTX (48 hours), without any signs of acute kidney injury; >= 2 micro mol/L
  • Time elapsed after administration of MTX (48 hours), with any sign of acute kidney injury; >= 0.4 micro mol/L

排除标准

  • 1.Patients with a history of serious hypersensitivity to any of the ingredients of OP-07
  • 2.Any patients for whom the investigator or subinvestigator considered the risks outweighing the benefits of dosing OP-07

结局指标

主要结局

Blood MTX concentration

时间窗: 48 hours

48 hours after the initial dose of OP-07

次要结局

未报告次要终点

研究者

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