跳至主要内容
临床试验/NL-OMON55829
NL-OMON55829已完成3 期

A 52-Week, open-label, single-arm study to evaluate the safety and tolerability of 24-hour daily exposure of continuous subcutaneous infusion of ABBV-951 in subjects with Parkinson*s disease - M15-741

AbbVie Deutschland GmbH & Co. KG0 个研究点目标入组 6 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
6

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
18 至 99(—)

入选标准

  • Adult male or female subjects, 30 years of age or older at the time of
  • screening, with a diagnosis of idiopathic PD that is levodopa-responsive

排除标准

  • Subjects judged by the investigator to be adequately controlled by current
  • therapy, that don't have recognizable/identifiable Off and On states (motor
  • fluctuations), and have less than 2.5 hours of Off time per day.

研究者

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