Open Label and Placebo-Controlled Assessment of Sublingual Apomorphine (Kynmobi) as Adjunct Therapy for Patients With Refractory Restless Legs Syndrome
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 16
- 试验地点
- 1
- 主要终点
- Visual Analogue Scale of Improvement
研究概览
简要总结
This is an open label, short placebo-controlled trial in Restless Legs Syndrome (RLS) patients inadequately treated with standard therapy. Investigators hypothesize that the study drug, sublingual apomorphine (Kynmobi), may improve RLS breakthrough symptoms. This study is designed to determine if sublingual apomorphine improves breakthrough symptoms in RLS patients, in addition to subjective responses.
详细描述
This is an open label, with a short placebo-controlled portion trial using sublingual apomorphine (Kynmobi) in RLS patients inadequately treated with standard therapy, defined by an IRLS > 15 and report of breakthrough symptoms.
At the initial visit, subjects will undergo all baseline and exploratory assessments and be given their first drug dose of 10 mg. They will be monitored for 60 minutes after dose. Subjects orthostatic blood pressure will be taken before ingestion, then 10, 20, 30, and 45 minutes after ingestion. Over the next 4 weeks, subjects will titrate Kynmobi to find optimal dose. Subjects will be instructed to take at least 2 doses before determining if further titration is needed.
At week 4, subjects will return for exploratory assessments. Subjects will be given a randomized study drug packet containing 2 placebos and 2 drug doses. Subjects will be told that 0-4 doses may be placebo or drug. Subjects will have 4 weeks to complete randomization doses. It is anticipated subjects will complete randomization sooner, so they will be given 23 doses of study drug (1 dose per 24 hours for 23 extra days until next visit).
At week 8, subjects will return for exploratory assessments and be given an additional 74 dosed strips. They will return at week 16 for a final visit and undergo exploratory assessments, followed by a safety call two weeks later.
From weeks 0-8, subjects are able to continue their scheduled RLS medications. From weeks 8-16, subjects may make changes to their RLS medications as mutually agreed upon with investigator.
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
- Single (Participant)
入排标准
- 年龄范围
- 21 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Idiopathic RLS diagnosed by standard criteria, with an IRLS > 15 while taking at least 1 RLS medication
- •Stable RLS medications for at least 2 weeks prior to study entry
排除标准
- •Concurrent untreated sleep disorders, not felt to be able stable
- •Subjects with any significant, unstable cardiovascular, liver, lung, renal. psychiatric, or neurological diseases (not including RLS)
- •Any medical or psychiatric comorbidity that, in the opinion of the investigator, would make study compliance difficult to achieve
- •Intravenous iron within 4 weeks of study entry
- •Breast feeding or pregnancy determined by urine pregnancy test in subjects where pregnancy is a possibility (pre-menopausal, sexually active women)
- •Subjects with previous allergic reaction to apomorphine or sulfate sensitivity
- •Subjects currently taking 5HT3 antagonists
研究组 & 干预措施
Sublingual Apomorphine (Kynmobi)
Sublingual apomorphine to be titrated after initial dose of 10 mg. Titration is dependent on subjects response.
干预措施: Apomorphine Sublingual Film (Drug)
Placebo
At week 4, subjects will be given randomization packet including 2 drug doses and 2 placebos.
干预措施: Apomorphine Sublingual Film (Drug)
Placebo
At week 4, subjects will be given randomization packet including 2 drug doses and 2 placebos.
干预措施: Placebo (Drug)
结局指标
主要结局
Visual Analogue Scale of Improvement
时间窗: Weeks 4 - 8
Subjects will assess how they feel 30 minutes after taking four doses of drug or placebo.
次要结局
- International RLS Rating Scale (IRLS)(Baseline, 4 weeks, 8 weeks, and 16 weeks)
- Hamilton Depression Scale (HDS)(Baseline, 4 weeks, 8 weeks, and 16 weeks)
- Clinical Global Impressions - Change(1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 8 weeks, 12 weeks, 16 weeks, and 18-20 weeks)
- The Restless Legs Syndrome - 6 Scale (RLS-6)(Baseline, 4 weeks, 8 weeks, and 16 weeks)
- Restless Legs Syndrome Quality of Life Questionnaire (RLSQoL)(Baseline, 4 weeks, 8 weeks, and 16 weeks)
- Epworth Sleepiness Scale (ESS)(Baseline, 4 weeks, 8 weeks, and 16 weeks)
研究者
William Ondo, MD
Principal Investigator
The Methodist Hospital Research Institute