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.
The study is being conducted worldwide. It consists of 4 segments: * Segment A: 7-day run-in (screening) * Segment B: 12-week double blind treatment * Segment C: 40-week open treatment extension * Segment D: 2-week run-out period
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
1,155
oral administration
oral administration
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
Change from baseline of the mean pr-WASO (wake time after sleep onset using patient's sleep questionnaire)
Time frame: at week 12
Change from baseline of the mean of the FOSQ items 1 and 2 (concentration/memory)
Time frame: at week 12
Change from baseline of the mean of the FOSQ items 4 and 10 (hobby/work)
Time frame: at week 12
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
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
...and 4 more locations