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NCT00308503: EPOCH

Efficacy and Safety of Eplivanserin 5mg/Day on Sleep Maintenance Insomnia: A 6 Week, Multicenter, Randomized, Double -Blind, Placebo-controlled Study

Completed Phase 3 Last updated 29 November 2010
What this trial tests

Phase 3 trial testing eplivanserin (SR46349) in Sleep Initiation and Maintenance Disorders in 608 participants. Completed in 1 August 2007.

Timeline
1 February 2006
Primary endpoint
1 August 2007
1 August 2007

Quick facts

Lead sponsorSanofi
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment608
Start date1 February 2006
Primary completion1 August 2007
Estimated completion1 August 2007
Sites3 locations across United States, Australia, Canada

Drugs / interventions tested

Conditions studied

Sponsor

Sanofi — full company profile →

Who can join

18 and older, any sex, with Sleep Initiation and Maintenance Disorders or Insomnia. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Sleep Initiation and Maintenance Disorders

Currently open trials in the same condition.

Other Sanofi trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00308503.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing