Efficacy and Safety of Eplivanserin Treatment for Sleep Maintenance Insomnia Followed by Optional Extension up to 1 Year

Completed · Phase 3 · Has a placebo group

Conditions studied: Sleep Initiation and Maintenance Disorders, Insomnia

In brief

The purpose of the study is to assess efficacy and safety of eplivanserin in the population of patients complaining of sleep maintenance insomnia. The patients suffering from that condition frequently wake up during the night, their sleep is nonrestorative and they suffer from a significant distress or impairment in their daily activities consecutive to insomnia.

Key facts

Study ID

NCT00253903

Run by

Sanofi

People needed

1155

Starts

2005-11-01

Expected to finish

2008-09-01

Last updated by the study team

2010-11-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Out patients
• Each patient must have primary insomnia in accordance with DSM-IV-TR-Axis I criteria
• Based on patient's information, the patient has spent at least 6.5 hours and not more than 9.0 hours, in bed, each night, over the preceding two weeks.
• Based on patient's information, the patient must complain of at least one hour of wakefulness after sleep onset for at least 3 nights per week over the preceding month
• Patient must report impact daytime functioning associated with sleep maintenance insomnia as measured by question 3 of Insomnia Severity Index at screening visit and randomization visit.

You may not qualify if…

• Females who are lactating or pregnant
• Woman of childbearing potential with a positive serum beta human chorionic gonadotropin pregnancy test at screening and not using an acceptable form of contraception
• Patients presenting with acute or chronic pain resulting in insomnia
• Patients with history of epilepsy or seizures
• Consumption of xanthine containing beverage (i.e. tea, coffee, or cola) comprising more than 5 glasses/day
• Evidence of any clinically significant, severe, or unstable acute or chronically progressive medical or surgical disorder which may affect patient safety
• BMI >32
• Acute or chronic pain resulting in insomnia
• Patients with current psychiatric disorders according to DSM-IV-TR criteria, mental retardation, or dementia
• Clinically significant and abnormal EKG (QTc interval >500 msec)
• Positive for hepatitis B or C
• Serious head injury or stroke within 1 year
• Use of OTC medications such as valerian root, kava, melatonin, St. John's Wort, or alluna; prescription sleep medications or anxiolytics within 1 week or 5 half-lives
• Participation in another trial within two month before the screening visit
• Use of any substance with psychotropic effects or properties known to affect sleep/wake
• Unable to complete the study questionnaires
• Night shift workers, and individuals who nap 3 or more times per week over the preceding month
• History of:
• Primary hypersomnia
• Narcolepsy
• Breathing-related sleep disorder (such as sleep apnea)
• Circadian rhythm sleep disorder
• Parasomnia (somnambulism)
• Dyssomnia (such as periodic leg movements)

Where it is running

• Sanofi-Aventis Administrative Office — Bridgewater, New Jersey, United States
• Sanofi-Aventis Administrative Office — Buenos Aires, Argentina
• Sanofi-Aventis Administrative Office — Macquarie Park, New South Wales, Australia
• Sanofi-Aventis Administrative Office — Vienna, Austria
• Sanofi-Aventis Administrative Office — Laval, Quebec, Canada
• Sanofi-Aventis Administrative Office — Santiago, Chile
• Sanofi-Aventis Administrative Office — Prague, Czechia
• Sanofi-Aventis Administrative Office — Helsinki, Finland
• Sanofi-Aventis Administrative Office — Paris, France
• Sanofi-Aventis Administrative Office — Berlin, Germany
• Sanofi-Aventis Administrative Office — México, Mexico
• Sanofi-Aventis Administrative Office — Gouda, Netherlands
• Sanofi-Aventis Administrative Office — Barcelona, Spain
• Sanofi-Aventis Administrative Office — Guildford, United Kingdom

Full record on ClinicalTrials.gov

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