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NCT00263042 · ClinicalTrials.gov registry record · Phase 3

Comprehensive Rimonabant Evaluation Study of Cardiovascular ENDpoints and Outcomes

A Phase 3 study, sponsored by Sanofi.

Terminated
Registry status
Phase 3
Development phase
18,695
Enrollment target

NCT00263042: Clinical Trial Phase 3 study, sponsored by Sanofi.

NCT00263042 is a Phase 3 study that was terminated before completion, run by Sanofi. The registered enrollment target is 18,695 participants, above the 771-participant average among 15,282 other Phase 3 trials with a reported enrollment target (2325% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00263042, a Phase 3 study, was terminated before completion, sponsored by Sanofi.

TERMINATED
Registry status
Phase 3
Development phase
18,695 participants
Enrollment target

Study Summary

The primary objective is to show whether rimonabant reduces the risk of a heart attack (MI), stroke, or death from an MI or stroke in patients with abdominal obesity with other cardiovascular (CV) risk factors. The secondary objective is to show whether rimonabant reduces the risk of MI, stroke, CV death, or CV hospitalization in these patients.

Interventions

  • DRUG Rimonabant
  • DRUG Placebo (for Rimonabant)

Trial Details

FieldValue
Enrollment Target 18,695 participants
Start Date 2005-12
Est. Completion 2009-04
Phase Phase 3
Sanofi

713 total trials

Why NCT00263042 stopped before completion

NCT00263042 is an interventional study that assigns participants to a tested intervention. Its 18,695 participants enrollment target places it among the larger protocols in the corpus, above the 771-participant average among 15,282 other Phase 3 trials with a reported enrollment target (2325% higher).

The record links to 0 conditions, and to 2 interventions - of which Rimonabant is the first listed.

NCT00263042 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00263042 about?

NCT00263042 is a clinical study titled "Comprehensive Rimonabant Evaluation Study of Cardiovascular ENDpoints and Outcomes". The primary objective is to show whether rimonabant reduces the risk of a heart attack (MI), stroke, or death from an MI or stroke in patients with abdominal obesity with other cardiovascular (CV) risk factors. The secondary objective is to show whether rimonabant reduces the risk of MI, stroke, CV...

What is the current status of trial NCT00263042?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 18,695 participants. The study started on 2005-12. Estimated completion is 2009-04.

What interventions are being tested in trial NCT00263042?

The interventions under investigation include: Rimonabant (DRUG), Placebo (for Rimonabant) (DRUG).

Who is sponsoring clinical trial NCT00263042?

This trial is sponsored by Sanofi, which has 713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00263042's enrollment target sits among peer trials

18,695 11th of 2000 higher than 1,990 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00263042, the US trial registry maintained by the National Library of Medicine. NCT00263042 (large enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.