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临床试验/NCT01085266
NCT01085266终止3 期

HORIZON-Plus: An Open-Label Extension of the HORIZON Protocol (DIM20) Evaluating the Safety of Dimebon (Latrepirdine) in Subjects With Huntington Disease

Medivation, Inc.0 个研究点目标入组 362 人开始时间: 2010年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
362

研究概览

简要总结

An open-label extension study of the HORIZON protocol evaluating the safety of dimebon (latrepirdine)in subjects with Huntington disease.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
30 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Successful completion of 26 weeks of blinded treatment in the HORIZON study

排除标准

  • Any other medical illness or unstable medical condition that may interfere with their ability to comply with study procedures and abide by study restrictions, or may interfere with the ability to interpret safety information.

研究组 & 干预措施

Dimebon (latrepirdine)

Experimental

Patients receive dimebon 10mg orally 3 times per day for 1 week and 20 mg orally 3 times per day thereafter.

干预措施: Dimebon (latrepirdine) (Drug)

研究者

申办方类型
Industry
责任方
Sponsor

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