跳至主要内容
临床试验/CTIS2023-507351-29-00
CTIS2023-507351-29-00进行中(未招募)1 期

A 52-Week, Open-Label Extension Study of ACP-204 in Adults with Alzheimer's Disease Psychosis - ACP-204-008

Acadia Pharmaceuticals Inc.0 个研究点目标入组 752 人开始时间: 2024年2月9日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
752

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Subject has successfully completed ACP-204-006 study, Male or female (age 55 to 85 years old): female must be of non-childbearing potential, male must take appropriate contraceptive method if partner has childbearing potential, Subject has a designated study partner/caregiver, Subjects are able to complete all study visits with a study partner/caregiver, Signed inform consent form with a caregiver or legal representative

排除标准

  • Requires treatment with a medication prohibited by the protocol, Is in hospice and receiving end-of-life palliative care, or has become bedridden, Female who is pregnant or breastfeeding, Unstable clinically significant medical condition other than AD, Any medical condition that in the opinion of the investigator may affect safety or ability to complete the study

研究者

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