Phase 3 Double-blind Placebo-controlled Parallel Group Study of Isradipine as a Disease Modifying Agent in Subjects With Early Parkinson Disease
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 336
- 试验地点
- 54
- 主要终点
- Adjusted Mean Change in Total Unified Parkinson Disease Rating Scale (UPDRS) Score
研究概览
简要总结
The purpose of the study is to determine whether treatment with isradipine is effective in slowing the progression of Parkinson disease disability.
详细描述
The study will enroll 336 participants in this multi-center study at approximately 56 sites across the US and Canada. In this study, we are comparing 10 mg of Isradipine to Placebo for treatment of newly diagnosed PD patients. Isradipine has been approved by the Food and Drug Administration (FDA) to treat high blood pressure but is considered investigational in this study, as it has not been approved for use in patients with PD.Isradipine can affect the function of specialized channels that are present in the types of brain cells that are affected in PD patient. These cells are usually responsible for making dopamine, which is depleted in patients with PD. Isradipine may block the damage caused by the flow of certain chemicals through these channels. Laboratory data has showed that Isradipine may prevent the development of Parkinson-like symptoms in animal studies. Isradipine has been evaluated in some patients with PD. The first study with isradipine controlled release (CR) in patients with early PD and normal blood pressure found that the drug was reasonably well tolerated and safe. The controlled release formulation of isradipine is not available for use and therefore this study is using the immediate release formulation. Eligible participants will be followed for up to 36 months and will be expected to complete 12 in-person visits and 4 telephone visits. The study visits will include clinical assessment of motor, neuropsychiatric and cognitive testing as well as collection of blood and urine samples. Study drug will taken twice daily, in the morning and in the evening with or without food. Prior to taking study drug, study participants will be required to take their blood pressure with a home blood pressure device provided to them for use in this study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 30 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects with early idiopathic PD (presence of at least two out of three cardinal manifestations of PD). If tremor is not present, subjects must have unilateral onset and persistent asymmetry of the symptoms
- •Age equal or greater than 30 years at the time of diagnosis of PD
- •Hoehn and Yahr stage less than or equal to 2
- •Diagnosis of PD less than 3 years.
- •Currently NOT receiving dopaminergic therapy (levodopa, dopamine agonist or MAO-B inhibitors) and NOT projected to require PD symptomatic therapy for at least 3 months from the baseline visit
- •Use of amantadine and/or anticholinergics will be allowed provided that the dose is stable for 8 weeks prior to the baseline visit
- •If subject is taking any central nervous system acting medications (e.g., benzodiazepines, antidepressants, hypnotics) regimen must be stable for 30 days prior to the baseline visit
- •Women of childbearing potential may enroll but must use a reliable measure of contraception and have a negative serum pregnancy test at the screening visit
排除标准
- •Subjects with a diagnosis of an atypical Parkinsonism
- •Subjects unwilling or unable to give informed consent
- •Exposure to dopaminergic PD therapy within 60 days prior to baseline visit or for consecutive 3 months or more at any point in the past
- •History of clinically significant orthostatic hypotension or presence of orthostatic hypotension at the screening or baseline visit defined as greater than or equal to 20 mmHg change in systolic BP and greater than or equal to 10 mmHg change in diastolic BP from sitting position to standing after 2 minutes, or baseline sitting BP less than 90/60
- •History of congestive heart failure
- •Clinically significant bradycardia
- •Presence of 2nd or 3rd degree atrioventricular block or other significant ECG abnormalities that in the investigator's opinion would compromise participation in study
- •Clinically significant abnormalities in the Screening Visit laboratory studies or ECG
- •Presence of other known medical or psychiatric comorbidity that in the investigator's opinion would compromise participation in the study
- •Prior exposure to isradipine or other dihydropyridine calcium channel blockers within 6 months of the baseline visit
- •Subjects on greater than 2 concomitant antihypertensive medications. If a history of hypertension, then a maximum of 2 other antihypertensive agents will be allowed provided that the dosages of concomitant anti HTN therapy can be reduced/adjusted during the study based on the BP readings in consultation with the subject's primary care provider or cardiologist. Use of any concomitant calcium channel blockers will not be allowed from the baseline visit and for the duration of the study
- •Use of grapefruit juice, ginkgo biloba, St. John's wort or ginseng will be prohibited starting from the screening visit and for the duration of the study (as they interfere with the metabolism of isradipine)
- •Use of clarithromycin, telithromycin and erythromycin will be prohibited starting from the screening visit and for the duration of the study as the combination of clarithromycin, telithromycin or erythromycin and calcium channel blockers has been reported to be associated with increased risk of kidney and heart injury
- •Presence of cognitive dysfunction defined by a Montreal Cognitive assessment (MoCA) score of less than 26 at screening
- •Subjects with clinically significant depression as determined by a Beck Depression Inventory II (BDI) score greater than 15 at the screening visit
- •History of exposure to typical or atypical antipsychotics or other dopamine blocking agents within 6 months prior to the baseline visit
- •History of use of an investigational drug within 30 days prior to the screening visit
- •History of brain surgery for PD
- •Allergy/sensitivity to isradipine or its matching placebo or their formulations
- •Pregnant or lactating woman
研究组 & 干预措施
Isradipine
Oral capsule of up to 5 mg of isradipine taken twice daily for 36 months.
干预措施: Isradipine (Drug)
Placebo (for Isradipine)
Oral capsule taken twice daily for 36 months.
干预措施: Placebo (for Isradipine) (Drug)
结局指标
主要结局
Adjusted Mean Change in Total Unified Parkinson Disease Rating Scale (UPDRS) Score
时间窗: Baseline to 36 months of treatment
Efficacy of isradipine to slow progression of Parkinson disease disability to be determined by the change in the total (Part I-III) UPDRS score in the active treatment arm versus placebo between the baseline and 36 month visit. The change of UPDRS ranges from -30 to 80, larger value shows more disability from PD.
Adjusted Mean Change in Adjusted UPDRS Score
时间窗: Baseline to 36 months of treatment
Efficacy of isradipine to slow progression of Parkinson disease disability to be determined by the change in the adjusted UPDRS Score in the active treatment arm versus placebo between the baseline and 36 month visit. The change of adjusted UPDRS ranges from -100 to 150, larger value shows more disability from PD.
次要结局
- Adjusted Mean Change in UPDRS Part IV(Baseline to 36 months of treatment)
- Adjusted Mean Change in Modified Rankin Score(Baseline to 36 months of treatment)
- Adjusted Mean Change in MoCA Score(Baseline to 36 months of treatment)
- Adjusted Mean Change in PDQ39 Total Score(Baseline to 36 months of treatment)
- Adjusted Mean Change in BDI Total Score(Baseline to 36 months of treatment)
- Risk of Need for Dyskinesia(Baseline to 36 months of treatment)
- Risk of Need for Fluctuations(Baseline to 36 months of treatment)
- Adjusted Mean Change in UPDRS Score to 1 Year(Baseline to 12 months of treatment)
- Adjusted Mean Change in LED(Baseline to 36 months of treatment)
- Adjusted Mean Change in LED Cumulative(Baseline to 36 months of treatment)
- Adjusted Mean Change in MDS-UPDRS nmEDL(Baseline to 36 months of treatment)
- Adjusted Mean Change in MDS-UPDRS mEDL(Baseline to 36 months of treatment)
- Adjusted Mean Change in UPDRS Part II(Baseline to 36 months of treatment)
- Adjusted Mean Change in UPDRS Part III OFF(Baseline to 36 months of treatment)
- Adjusted Mean Change in SE/ADL(Baseline to 36 months of treatment)
- Adjusted Mean Change in Ambulatory Capacity(Baseline to 36 months of treatment)
- Risk of Need for Antiparkinsonian Therapy(Baseline to 36 months of treatment)
研究者
Robert Holloway
Principal Investigator
University of Rochester