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パーキンソン病(PD)の日本人成人患者を対象としたLu AF28996の臨床試験
基本情報
- NCT ID
- NCT06004180
- ステータス
- 完了
- 試験のフェーズ
- 第1相
- 試験タイプ
- 介入
- 目標被験者数
- 6
- 治験依頼者名
- H. Lundbeck A/S
概要
This trial will evaluate the effects of Lu AF28996 in adult Japanese men and women with Parkinson's disease (PD). The main goals of the trial are to learn more about a) the safety and tolerability of Lu AF28996 (any new or worsening medical issues the participants have with treatment), and b) the pharmacokinetic parameters of Lu AF28996 (how the drug is absorbed, distributed, and processed by the body). Participants will take Lu AF28996 capsules orally once a day (OD). The participants will start with a low dose of Lu AF28996, which will be increased gradually over a period of 2 weeks, and then decreased gradually over a period of about 2 weeks.
対象疾患
Parkinson Disease
介入
Lu AF28996(DRUG)
依頼者(Sponsor)
H. Lundbeck(INDUSTRY)
実施施設 (1)
愛媛大学医学部附属病院
Ehime, Japan