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NCT00250653 · ClinicalTrials.gov registry record · Phase 3

A Fifty-two-week Study to Evaluate the Safety of Saredutant in Adult and Elderly Patients With Depression

A Phase 3 study, sponsored by Sanofi.

Completed
Registry status
Phase 3
Development phase
365
Enrollment target

NCT00250653 is a Phase 3 study that has completed, run by Sanofi. The registered enrollment target is 365 participants.

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The verdict

NCT00250653, a Phase 3 study, has completed, sponsored by Sanofi.

COMPLETED
Registry status
Phase 3
Development phase
365 participants
Enrollment target

Study Summary

The purpose of the study is to evaluate the long-term safety of saredutant (or SR48968C) in adult and elderly patients with depression.The primary objective is to evaluate the long-term safety and tolerability of a 100 mg dose of saredutant in adult and elderly patients with depression. The secondary objective is to evaluate blood levels of saredutant.

Interventions

  • DRUG Saredutant succinate (SR48968C)

Trial Details

FieldValue
Enrollment Target 365 participants
Start Date 2005-05
Est. Completion 2007-04
Phase Phase 3

Sponsor

Sanofi

713 total trials

What the Registry Record Tells You About NCT00250653

The ClinicalTrials.gov registry entry for NCT00250653 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 365 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sanofi, which has 713 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Saredutant succinate (SR48968C) is the first listed.

NCT00250653 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00250653 about?

NCT00250653 is a clinical study titled "A Fifty-two-week Study to Evaluate the Safety of Saredutant in Adult and Elderly Patients With Depression". The purpose of the study is to evaluate the long-term safety of saredutant (or SR48968C) in adult and elderly patients with depression.The primary objective is to evaluate the long-term safety and tolerability of a 100 mg dose of saredutant in adult and elderly patients with depression. The secondar...

What is the current status of trial NCT00250653?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 365 participants. The study started on 2005-05. Estimated completion is 2007-04.

What interventions are being tested in trial NCT00250653?

The interventions under investigation include: Saredutant succinate (SR48968C) (DRUG).

Who is sponsoring clinical trial NCT00250653?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.