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临床试验/JPRN-jRCT2051220026
JPRN-jRCT2051220026招募中2 期

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

Watanabe Tatsuo0 个研究点目标入组 10 人开始时间: 2022年5月25日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
10

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
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 1. Patients whose written informed consent to participate in this study has been obtained from the patient or his/her legally authorized representative
  • 2. 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/

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

研究者

发起方
Watanabe Tatsuo

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