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临床试验/CTRI/2009/091/000522
CTRI/2009/091/000522已完成未知

TRA108132 : LENS - Long-Term Eltrombopag Observational Study - A Long Term Observational Ocular Safety Follow-up Study in Adults Who Have Received Study Medication (SB-497115-GR / Eltrombopag Olamine or Placebo) in a Phase II or III Clinical Study Evaluating Eltrombopag

GlaxoSmithkline Pharmaceuticals Ltd0 个研究点目标入组 150 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
150

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Inclusion Criteria:
  • Subjects are eligible for enrolment in the study if they have previously participated in an eltrombopag study, either phase II or III, and meet all of the following criteria:
  • Subject has signed and dated a written informed consent for this study.
  • Subject has previously participated in a study evaluating eltrombopag, either phase II or III, and must have received at least one dose of study medication (either active drug or placebo). This excludes subjects from phase I studies.
  • The prescribed follow-up ophthalmic assessment at 6 months post end of treatment should be completed as specified in the protocol for the previous study.
  • Subject is able to understand and comply with protocol requirements and instructions.

排除标准

  • Exclusion Criteria:
  • Subjects meeting any of the following criteria must not be enrolled in the study:
  • Subject has received surgery for cataracts and is aphakic or bilaterally pseudophakic.

研究者

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