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COMPLETED Phase 2

A Safety, Efficacy and Tolerability Study of SEP-225289

NCT00584974 · View on ClinicalTrials.gov ↗

Study Summary

To determine the safety, efficacy and tolerability of SEP-225289 in subjects with Major Depressive Disorder

Conditions Studied

Interventions

  • DRUG placebo
  • DRUG SEP-225289
  • DRUG Venlafaxine

Study Locations (20)

California

  • — Arcadia
  • — Beverly Hills
  • — Costa Mesa
  • — Garden Grove
  • — Glendale
  • — Irvine
  • — Lafayette
  • — Oceanside
  • — San Diego
  • — Upland

Florida

  • — Bradenton
  • — Fort Myers
  • — Jacksonville
  • — Lauderhill
  • — Maitland
  • — North Miami

Colorado

  • — Denver
  • — Denver

Arkansas

  • — Little Rock

Connecticut

  • — New Britain

Trial Details

FieldValue
Enrollment Target 523 participants
Start Date 2007-12
Est. Completion 2009-05
Phase Phase 2

Sponsor

Sumitomo Pharma America

65 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00584974

The ClinicalTrials.gov registry entry for NCT00584974 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 523 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sumitomo Pharma America, which has 65 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Depressive Disorder, Major appearing as the primary indexed condition, and to 3 interventions — of which placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00584974 reports 20 study locations spanning 5 distinct geographic areas — top geographies include California, Florida, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00584974 about?

NCT00584974 is a clinical study titled "A Safety, Efficacy and Tolerability Study of SEP-225289". To determine the safety, efficacy and tolerability of SEP-225289 in subjects with Major Depressive Disorder

What is the current status of trial NCT00584974?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 523 participants. The study started on 2007-12. Estimated completion is 2009-05.

What conditions does trial NCT00584974 study?

This clinical trial studies the following conditions: Depressive Disorder, Major. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00584974?

The interventions under investigation include: placebo (DRUG), SEP-225289 (DRUG), Venlafaxine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00584974?

This trial is sponsored by Sumitomo Pharma America, which has 65 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00584974 being conducted?

This trial has 20 study locations across Arkansas, California, Colorado, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial