NCT04455555已完成3 期
Efficacy and Safety of Rotigotine in the Treatment of Patients With Early Stage of Primary Parkinson's Disease
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 294
- 试验地点
- 1
- 主要终点
- Changes in the total Unified Parkinson Disease Rating Scale (UPDRS) (II +III) score
研究概览
简要总结
The efficacy and safety of rotigotine in the treatment of patients with early stage of primary Parkinson's disease
详细描述
To evaluate the efficacy and safety of rotigotine sustained release microspheres therapy by injection in the treatment of patients with early stage of primary Parkinson's disease
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)
盲法说明
participant and investigator
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects or their legal representatives understand and wish to participate in this clinical study and voluntarily sign the informed consent dated;
- •In the investigator's judgment, believe that the subject or his legal representative is trustworthy and able to comply with the study protocol, visit plan, or receive the study drug treatment as required;
- •During screening (interview 1) The subjects were older than 30 years old, regardless of gender;
- •The subject had primary Parkinson's disease for 55 years and was diagnosed based on major signs such as delayed movement and at least one of the following symptoms: quiescence tremor, rigidity or postural reflexes, and no other known or suspected cause of Parkinson's disease;
- •Hoehn-yahr stage 3 in the "open" state (excluding phase 0);
- •Brief mental State examination (MMSE) ≥ 25;
- •At baseline (visit 2), the exercise score (Part III) of the Unified Parkinson's Disease Rating Scale (U PDRS) under the "open" condition was greater than or equal to 10;
- •If the subjects are receiving anticholinergic drugs (such as benzalkonium tropic, benzene hai suo, diethyl promethazine, its organism and than pp board), monoamine oxidase B (MAO B) inhibitors, N - Methyl - d - aspartate (NMDA) antagonist (such as amantadine) treatment, must dose before baseline visit (2) is stable at least 28 days, and maintain the dose treatment during the study period;
- •Childbearing age women (such as: no sterilization surgery or postmenopausal women is less than 1 year) or male subjects agreed to during the entire study (screening visit to the end of the study) and reliable contraceptive measures (birth control pills, use a condom, abstinence, etc.), and the screening visit (l) and the baseline visit (2), the childbearing age women of pregnancy test results were negative.
排除标准
- •A history of globulin resection, thalamic destruction, deep brain stimulation or fetal tissue transplantation;
- •Dementia, active mental illness or hallucinations, major depression
- •Those who received dopamine agonist within 28 days before baseline (visit 2);
- •Those who received levodopa preparations (including levodopa compound preparations) within 28 days before baseline (visit 2), or those who received levodopa preparations for more than 6 months after diagnosis; Patients who received any of the following drugs: amphetamine or alpha within 28 days prior to baseline (visit 2)
- •Receiving Central nervous system active drug therapy (e.g., tranquilizers, sleeping pills, antidepressants, antianxiety medications), except for those who have been on a stable dose for at least 28 days prior to baseline (visit 2) and are likely to remain stable during the study period;
- •Atypical Parkinson's disease symptoms caused by the use of drugs (e.g., metoclopramide, flunarizine), hereditary metabolic diseases of the nervous system (e.g., Wilson's disease), encephalitis, cerebrovascular diseases, or degenerative diseases (e.g., progressive supranuclear palsy);
- •Patients with a history of epilepsy, or with a history of stroke or transient ischemic stroke within 1 year before the visit;
- •Intolerance or allergy to antiemetic drugs such as domperidone, ondansetron, tropisetron, granisetron;
- •Patients with clinically significant liver function abnormalities are defined as 1.5 times of the upper limit of the reference range of total bilirubin > or 2 times of the upper limit of the reference range of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >;
- •Abnormal renal function with clinical significance (serum creatinine > 2.0 mg/dL);
- •Uncontrolled or significant cardiovascular disease, including New York Heart Association grade 2 or above congestive heart failure, unstable angina, myocardial infarction, or arrhythmias requiring treatment at screening (visit 1) in the 6 months prior to first administration of the study drug;
- •During screening (interview I);
- •A history of symptomatic postural hypotension; Systolic blood pressure reduction greater than or equal to 20 MMHG or diastolic blood pressure reduction greater than or equal to 10 mmHg during screening (visit l) and baseline (visit 2) from baseline to upright position for 1 or 3 minutes; Or patients with horizontal systolic blood pressure < 105 mmHg during screening (visit I) and baseline (visit 2);
- •Subjects with evidence of impulse control disorder (ICD) during screening (interview L);
- •A history of suicide attempt (including actual attempt, interruption of attempt or failure of attempt) or suicidal ideation in the past 6 months, defined as "yes" to question 4 or 5 on the Columbine Suicide Severity Rating Scale (C-SSRS) at screening (interview L); those
- •Patients with a history of narcolepsy;
- •Screening (interview L) For those who had a history of alcohol abuse, drug abuse or drug addiction in the first 5 years, alcoholism was defined as drinking more than 14 units of alcohol per week (1 unit = 360 ml beer or 45 ml spirits with 40% alcohol or 150 ml wine);
- •Screening for malignant tumors within 5 years before surgery, except adequately treated carcinoma in situ of the cervix, basal cell or squamous cell carcinoma of the skin, local prostate cancer after radical surgery, and intraductal carcinoma in situ of the breast;
- •Women during pregnancy or lactation;
- •Previous participants in the Rotigotine trial were intolerant or had poor efficacy;
- •Allergic to or known to be allergic to rotigotine or rotigotine microsphere preparations;
- •Those who have participated in other drug clinical trials within 3 months prior to screening;
- •Any other medical condition, mental condition, or laboratory abnormality of clinical significance that the investigator determines may interfere with the subject's ability to participate in the study.
研究组 & 干预措施
rotigotine treatment group
Experimental
rotigotine sustained release microspheres therapy by injection
干预措施: LY03003( the name of rotigotine) (Drug)
placebo comparator
Placebo Comparator
placebo comparator/null microspheres
干预措施: Placebo (Other)
结局指标
主要结局
Changes in the total Unified Parkinson Disease Rating Scale (UPDRS) (II +III) score
时间窗: 32 weeks after treatment
Changes in the total Unified Parkinson Disease Rating Scale (UPDRS) (II +III) score relative to baseline from baseline to the end of the double-blind dose maintenance period, The UPDRS scale refers to Unified Parkinson Disease Rating Scale, and it is a rating tool used to gauge the course of Parkinson's disease in patients. Some sections of the UPDRS scale require multiple grades assigned to each extremity with a possible maximum of 199 points. A score of 199 on the UPDRS scale represents the worst (total disability) with a score of zero representing (no disability).
次要结局
- changes in the severity (SI) score;(32 weeks after treatment)
- Changes in Beck Depression Inventory II (BDI-II) scores(32 weeks after treatment)
- Unified Parkinson Disease Rating Scale (UPDRS) maximum table (II +III) total score(32 weeks after treatment)
- changes in part II of the Unified Parkinson Disease Rating Scale relative to baseline(32 weeks after treatment)
- Changes in pd Questionnaire (PDQ-8) scores(32 weeks after treatment)
- Changes in pd sleep Disorders Scale (PDSS) score(32 weeks after treatment)
研究者
研究点 (1)
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