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The aim of the study is to confirm the efficacy of eplivanserin 5mg/day on sleep maintenance of patients with primary insomnia using night polysomnography recordings over a 6-week treatment period corresponding to a stabilization of improvement of sleep.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | 5 mg/day |
|
| 2 | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| eplivanserin (SR46349) | Drug | oral administration |
| |
| placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline of night polysomnography Wake Time After Sleep Onset (PSG WASO) | week 6 |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in general productivity domain of the FOSQ (Functional Outcome of Sleep Questionnaire) | week 6 | |
| Change from baseline in patient reported wake after sleep onset (pr-WASO) | week 6 |
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Inclusion Criteria:
Diagnosis of primary insomnia based on Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) criteria for at least one month preceding the study visit.
Disturbance of sleep maintenance:
Based on patient' s information:
Inclusion will be based on the nocturnal polysomnography (NPSG) recordings performed at the sleep laboratory during the two screening nights.
Exclusion Criteria:
Females who are lactating or who are pregnant, or of childbearing potential not using an acceptable form of contraception
Patients presenting with acute or chronic pain resulting in insomnia
Patients with current psychiatric disturbances
Body mass index > 32
Evidence of any clinically significant, severe or unstable, acute or chronically progressive medical or surgical disorder, or any condition that may interfere with the absorption, metabolism, distribution or excretion of the study drug, or may affect patient safety
Clinically significant and abnormal electrocardiogram (ECG) (including QTc B > 500ms),
A positive test for hepatitis B (hepatitis B surface [HBs] antigens) or C (hepatitis C virus [HCV] antibodies)
Positive qualitative urine drug screen at screening
Consumption of xanthine-containing beverages (i.e. tea, coffee, or cola) comprising usually more than 5 cups or glasses per day
Use of any over-the-counter or prescription sleep medication, or of any substance with psychotropic effects or properties known to affect sleep/wake, within one week or five half-lives (whichever is longer), prior to screening
Night shift workers, and individuals who nap 3 or more times per week over the preceding month
Based on medical history and/or NPSG:
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| Name | Affiliation | Role |
|---|---|---|
| ICD CSD | Sanofi | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sanofi-Aventis | Bridgewater | New York | 08807 | United States | ||
| Sanofi-Aventis |
| ID | Term |
|---|---|
| D007319 | Sleep Initiation and Maintenance Disorders |
| ID | Term |
|---|---|
| D020919 | Sleep Disorders, Intrinsic |
| D020920 | Dyssomnias |
| D012893 | Sleep Wake Disorders |
| D009422 | Nervous System Diseases |
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| ID | Term |
|---|---|
| C076033 | SR 46349B |
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| Drug |
oral administration |
|
| Macquarie Park |
| New South Wales |
| Australia |
| Sanofi-Aventis | Laval | Canada |
| D001523 |
| Mental Disorders |