Clinical trial

Comparison of Efficacy and Safety of Rimonabant 5mg/Day or 20mg/Day Versus…

NCT00464165 · Sanofi, Industry · Completed

Key facts

NCT number NCT00464165
Title Comparison of Efficacy and Safety of Rimonabant 5mg/Day or 20mg/Day Versus Placebo in Smoking Cessation
Official title Comparison of the Efficacy and Safety of 2 Oral Doses of Rimonabant, 5mg/Day or 20mg/Day, Versus Placebo, as an Aid to Smoking Cessation; Multiple Country, Randomized, Double-blind, 3-arm, 10-week Treatment, 40-week Follow-up
Acronym STRATUS-EU
Lead sponsor Sanofi, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Smoking Cessation
Intervention type Drug
Interventions rimonabant
Enrollment 789
Start date Nov 1, 2002
Primary completion Oct 1, 2003
Completion Oct 1, 2003
First posted Apr 23, 2007
Last update posted Dec 10, 2010
Countries Belgium, Denmark, France, Spain, Sweden, Switzerland, United Kingdom

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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