Clinical trial

Comparison of Efficacy and Safety of Rimonabant 20mg/Day Versus Placebo in…

NCT00464256 · Sanofi, Industry · Completed

Key facts

NCT number NCT00464256
Title Comparison of Efficacy and Safety of Rimonabant 20mg/Day Versus Placebo in Smoking Cessation
Official title Comparison of the Efficacy and Safety of a 20 mg/Day Oral Dose of Rimonabant Versus Placebo as an Aid to Smoking Cessation - a US, Randomized, Double-blind, 2 Arm, Placebo-controlled, Parallel-group, Fixed Dose, 12-week Study
Acronym STRATUS-META
Lead sponsor Sanofi, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Smoking Cessation
Intervention type Drug
Interventions rimonabant
Enrollment 533
Start date Apr 1, 2004
Primary completion Nov 1, 2004
Completion Nov 1, 2004
First posted Apr 23, 2007
Last update posted Dec 10, 2010
Countries United States

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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