Impact of Nilotinib on Safety, Biomarkers and Clinical Outcomes in Mild to Moderate Alzheimer's Disease
| 対象疾患 | Alzheimer's Disease |
|---|---|
| 相 | 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
| 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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- Brain Energy for Amyloid Transformation in Alzheimer's Disease Study — Wake Forest University Health Sciences
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- Deprescribing in Patients Living With Dementia With Caregiver and Provider Nudges — Brigham and Women's Hospital
- Technology and Family Thriving Study — University of California, Santa Barbara
- Community-based Brain Health Program to Address Dementia Risk — Posit Science Corporation