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临床试验/JPRN-jRCT2080221783
JPRN-jRCT2080221783未知2 期

A phase 2, open-label study of S-6810 in patients with mycosis fungoides or Sezary syndrome

SHIONOGI & CO., LTD.0 个研究点目标入组 15 人开始时间: 2012年5月10日最近更新:
适应症

试验速览

阶段
2 期
入组人数
15

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Main inclusion criteria
  • 1. Patients with mycosis fungoides or Sezary syndrome confirmed by cutaneous symptom, histopathological diagnosis or hematological evidence
  • 2. Patients whose TNMB staging criterion is T1-4N0-2M0B0-2 and meet any of the following:
  • a) untreated mycosis fungoides/Sezary syndrome
  • b) at least 4 weeks after treatment for mycosis fungoides/Sezary syndrome
  • c) the effect of topical steroid, topical vitamin D3 derivatives, or ultraviolet therapy for mycosis fungoides/Sezary syndrome is stable or progressive within 4 weeks
  • 3. Patients whose ECOG performance status is grade 0-2

排除标准

  • Main exclusion criteria:
  • Patients whose visceral metastasis was found by imaging evaluation within 4 weeks prior to enrollment

研究者

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