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临床试验/JPRN-jRCT2080222709
JPRN-jRCT2080222709已完成3 期

A Multicenter, Open-label, Long-term, Extension, Phase 3 Study to Evaluate the Safety and Efficacy of TVP-1012 at 1 mg in Early Parkinson's Disease Patients Not Treated with Levodopa

Takeda Pharmaceutical Company Limited0 个研究点目标入组 198 人开始时间: 2015年1月6日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
198

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
>= 30age old 至 <= 79age old(—)
性别
All

入选标准

  • The participant has completed the preceding study.
  • -The participant has shown no safety issues during the study treatment in the preceding study, in the opinion of the investigator or subinvestigator.

排除标准

  • -The participant has undergone blood collection of >= 400 mL within 90 days prior to the start of treatment in this study.
  • -The participant is required to take any of the excluded medications or treatments.
  • -The participant is required surgery or hospitalization for surgery during the study period.

研究者

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