跳至主要内容
临床试验/NCT06592014
NCT06592014Enrolling By Invitation1 期

Repurposing Lithium as a Disease-modifying Therapy in Parkinson's Disease: an Open-label Extension Trial.

State University of New York at Buffalo2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2024年8月9日最近更新:
适应症

试验速览

阶段
1 期
状态
Enrolling By Invitation
入组人数
35
试验地点
2
主要终点
Free Water

研究概览

简要总结

This study will examine the effects of 24 weeks of lithium therapy achieving serum lithium levels of 0.25-0.50mmol/L on MRI and blood-based biomarkers in Parkinson's disease patients who have completed one of our current 24-week lithium clinical trials.

详细描述

In observational studies, small daily doses of lithium from smoking cigarettes have been associated with a 77% reduced risk of developing Parkinson's disease (PD). In addition, lithium therapy has been effective in preventing neuronal death and behavioral symptoms in several PD animal models. Recently, our group has shown 24-weeks of low-dose lithium therapy in PD to be associated with improvements in both MRI and blood-based biomarkers implying that lithium may be slowing the progression of the disease. However, these findings stemmed from only three of four patients receiving MRIs. Our group is now conducting two larger studies enrolling a total of 35 PD patients who are being treated with either 45mg/day or 20mg/day of lithium or placebo therapy for 24 weeks. Because our earlier study showed maximum improvements in PD biomarkers in patients with serum lithium levels of 0.25-0.50mmol/L and there are large interpatient variations in serum lithium levels achieved from the same lithium dosage, this present study will adjust lithium dosing in each patient to achieve this target serum lithium level for an additional 24 weeks. MRI and blood-based biomarker changes from Baseline will be compared in patients with serum lithium levels ≥ 0.25mmol/L and <0.25mmol/L from one of the 24-week studies and within individual patients. Results from this study may identify a target serum lithium level range associated with maximum improvements in PD biomarkers that can be used in the design of future, larger lithium PD lithium trials, which may eventually support lithium as a disease-modifying therapy for PD that could improve patients' long-term prognoses.

研究设计

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

入排标准

年龄范围
45 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All PD patients completing STUDY00007253 or STUDY00008239 at the University at Buffalo will be eligible.
  • No unstable cardiac, medical, neurologic or psychiatric condition in the opinion of the PI.
  • No current use of illicit drugs or current alcohol abuse in the opinion of the PI.
  • No history of brain surgery or possible need for brain surgery including deep brain stimulation (DBS) for at least 24 weeks in the opinion of the PI.
  • Women with child bearing potential will need a negative pregnancy test and not be nursing an infant at screening. Women with child bearing potential will need to report using barrier method or hormonal contraception.
  • Willing and able to sign informed consent and follow study procedures.

排除标准

  • 未提供

结局指标

主要结局

Free Water

时间窗: 24 Weeks.

Change in MRI-assessed free water in posterior substantia nigra, dorsomedial nucleus of the thalamus and nucleus basalts of Meynert.

Serum neurofilament light chain

时间窗: 24 weeks

Change in serum neurofilament light chain

次要结局

  • Peripheral blood mononuclear cell (PBMC) Nurr1 mRNA levels by real-time polymerase chain reaction (PCR)(24 weeks)
  • PBMC superoxide dismutase 1 (SOD-1) mRNA levels(24 weeks)
  • PBMC phosphorylated (p) and total (t) levels of pS9 and total-glycogen synthase kinase 3B (GSK-3B)(24 weeks)
  • PBMC pThr308, pS473 and t-protein kinase B (Akt)(24 weeks)
  • Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS), Part III(24 weeks)
  • Parkinson's Anxiety Scale(24 weeks)
  • Geriatric Depression Scale-15(24 weeks)
  • Fatigue Severity Scale(24 weeks)
  • Insomnia Severity Index(24 weeks)
  • Parkinson's Disease Questionnaire-8(24 weeks)
  • Montreal Cognitive Assessment (MoCA)(24 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thomas Guttuso

Professor of Neurology

State University of New York at Buffalo

研究点 (2)

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