A phase III, double-blind, placebo-controlled, randomised trial to determine the efficacy and safety of a dose range of 50 to 100 mg/day of safinamide, as add-on therapy, in subjects with idiopathic Parkinson’s Disease with motor fluctuations, treated with a stable dose of levodopa and who may be receiving concomitant treatment with stable doses of a dopamine agonist, an anticholinergic and/or amantadine. - Safinamide in IPD with motor fluctuations, as add-on to levodopa
- Conditions
- Ideopathic Parkinson's DiseaseMedDRA version: 9.1 Level: LLT Classification code 10061536 Term: Parkinson's disease
- Registration Number
- EUCTR2007-002964-90-GB
- Lead Sponsor
- Merck Serono S.A - Geneva
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Not specified
- Target Recruitment
- 605
1. Diagnosis of idiopathic Parkinson’s Disease of more than 3 years duration, with a Hoehn and Yahr stage of I-IV during an off” phase. The diagnosis should be based on medical history and neurological examination.
2. Between the ages of 30 to 80 years, inclusive, at screening.
3. If female, be either post-menopausal for at least 2 years, surgically sterilised or have undergone hysterectomy or, if of child bearing potential, be willing to avoid pregnancy by using an adequate method of contraception as defined in Section 6.4.10 for four weeks prior to, during and four weeks after the last dose of trial medication. For the purposes of this trial, women of childbearing potential are defined as all female subjects after puberty unless they are post-menopausal for at least two years, are surgically sterile or are sexually inactive.
4. Be levodopa responsive and have been receiving treatment with a stable dose of levodopa [4-10 doses per day of any levodopa preparation (including CR, IR or a combination of CR/IR), plus benserazide/carbidopa; with or without addition of a COMT inhibitor] and may be receiving concomitant treatment with stable doses of a dopamine agonist, an anticholinergic and/or amantadine for at least 4 weeks prior to the screening visit.
5. Have motor fluctuations, with >1.5 hours off” time during the day (excluding morning akinesia).
6. Be able to maintain an accurate and complete diary (18-hour), with the help of a caregiver, recording on” time, on” time with minor dyskinesia, on” time with troublesome dyskinesia, off” time, and time asleep.
7. Willing and able to participate in the trial and has provided written, informed consent.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
1. Any indication of forms of parkinsonism, other than idiopathic Parkinson’s Disease.
2. If female, be pregnant or lactating
3. Be in a late stage of Parkinson’s Disease, and experiencing severe, disabling peak-dose or biphasic dyskinesia and/or unpredictable or widely swinging fluctuations in their symptoms.
4. Current diagnosis of substance abuse or history of alcohol or drug abuse in the past 3 months.
5. Current clinically significant gastrointestinal, renal, hepatic, endocrine, pulmonary or cardiovascular disease, including acute gastric ulcer, hypertension that is not well
controlled, asthma, chronic obstructive pulmonary disease (COPD), and Type I diabetes. Subjects with a history of gastric ulcer who have not had a recent episode of acute gastritis and are not currently experiencing gastric pain will be eligible for inclusion.
6. Second- or third-degree atrio-ventricular block or sick sinus syndrome, uncontrolled atrial fibrillation, severe or unstable angina, congestive heart failure, myocardial infarction within 3 months of the screening visit, or a significant ECG abnormality, including QTc U 450 msec (males) or U 470 msec (females), where QTc is based on Bazett’s correction method.
7. Have received treatment with safinamide previously.
8. Concomitant disease likely to interfere with the trial medication (e.g. capable of altering absorption, metabolism or elimination of the trial drug).
9. History of, or current psychosis (e.g. schizophrenia or psychotic depression), or a score greater than or equal to 3 on Item 2 (thought disorder) or 3 (depression) of the UPDRS Section I at screening.
10. Evidence of dementia or cognitive dysfunction, as indicated by a MMSE score < 22, or a score greater than or equal to 3 on item 1 (mentation) of the UPDRS, Section I at screening.
11. Depression, as indicated by a GRID-HAMD (17-item scale) score > 17 at screening.
12. History of allergic response to anticonvulsants, levodopa, or other anti-parkinsonian
agents.
13. Mental or physical condition (e.g., neurotic behaviour, crippling degenerative arthritis, or limb amputation), which would preclude performing efficacy or safety assessments.
14. Hypersensitivity or contraindications to MAO-B inhibitors.
15. Current history of severe dizziness or fainting on standing, due to postural hypotension.
16. Neoplastic disorder, which is either currently active or has been in remission for less than one year.
17. Stereotactic surgery as a treatment for his/her Parkinson’s Disease.
18. Participation in a clinical trial within 30 days of entry into the trial (screening visit) or having received treatment with any investigational compound within 30 days or 5 halflives, whichever is longer, prior to screening.
19. Treatment with any agent known to significantly inhibit or induce drug-metabolising enzymes (e.g., barbiturates, phenothiazines, etc.) within 4 weeks preceding the screening visit.
20. Treatment with opioids (e.g., tramadol, meperidine derivatives), SNRI’s (e.g. venlafaxine, duloxetine), tri- or tetra-cyclic antidepressants, MAO inhibitors (e.g. selegiline) in the 8 weeks prior to
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method