BENITIONSClinical Trial Intelligence

Impact of Nilotinib on Safety, Biomarkers and Clinical Outcomes in Mild to Moderate Alzheimer's Disease

第2相 完了 NCT02947893

対象疾患Alzheimer's Disease
第2相
スポンサーGeorgetown University
ステータス完了
参加者数37 名
介入(薬剤)Placebo Capsule(s) Once a Day by Mouth, Nilotinib Capsule(s) Once a Day by Mouth
開始日2017年1月
完了日2020年12月
結果公開日2026年7月23日

概要

The investigators hypothesize that Nilotinib will be safe in individuals with mild to moderate AD. Specifically, investigators hypothesize that low daily oral doses of Nilotinib will lead to CSF penetration, CNS Abl inhibition, and stabilization of CSF total Tau and p-Tau231/181 and Abeta42/40 levels. The investigators hypothesize that Nilotinib will decrease brain load of amyloid using amyloid positron emission tomography (PET). The investigators also predict that Nilotinib will reduce CSF markers of cell death, including neuron specific enolase (NSE) and S100B.

Safety Will be Measured by Number of Participants Experiencing the Occurrence of Adverse Events and/or Abnormal Laboratory Values

12 months · events

Group 1 (Placebo)2 events
Group 2 (Treated)0 events
Group 1 (Placebo)1 events
Group 2 (Treated)1 events
Group 1 (Placebo)1 events
Group 2 (Treated)0 events

BENITIONS で見る ClinicalTrials.gov の原文を見る

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このページは ClinicalTrials.gov の公開データをまとめたものです。医学的助言ではなく、投資助言でもありません。必ず専門医にご相談ください。