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Completed Phase 2 Interventional Results available

Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Adults With Fatigue Associated With Major Depressive Disorder

ClinicalTrials.gov ID: NCT01254305

Public ClinicalTrials.gov record NCT01254305. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 8, 2026, 8:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-blind, Randomized, Placebo- and Active-Controlled Study of F2695 SR in Adult Patients With Fatigue Associated With Major Depressive Disorder

Study identification

NCT ID
NCT01254305
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Forest Laboratories
Industry
Enrollment
262 participants

Conditions and interventions

Interventions

  • Levomilnacipran ER Drug
  • Paroxetine, Sertraline, Citalopram or Fluoxetine. Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2011
Primary completion
Jun 30, 2012
Completion
Jun 30, 2012
Last update posted
Aug 5, 2014

2011 – 2012

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Forest Investigative Site 010 Birmingham Alabama 35216
Forest Investigative Site 002 Little Rock Arkansas 72223
Forest Investigative Site 001 Cerritos California 90703
Forest Investigative Site 014 Fort Myers Florida 33912
Forest Investigative Site 006 Jacksonville Florida 32216
Forest Investigative Site 017 Orange City Florida 32763
Forest Investigative Site 005 Orlando Florida 32806
Forest Investigative Site 012 Tampa Florida 33613
Forest Investigative Site 009 Atlanta Georgia 30308
Forest Investigative Site 016 Joliet Illinois 60435
Forest Investigative Site 004 New Orleans Louisiana 70122
Forest Investigative Site 022 Boston Massachusetts 02135
Forest Investigative Site 015 Cedarhurst New York 11516
Forest Investigative Site 011 The Bronx New York 10467
Forest Investigative Site 003 Cincinnati Ohio 45227
Forest Investigative Site 013 Dayton Ohio 45417
Forest Investigative Site 020 Lincoln Rhode Island 02865
Forest Investigative Site 018 Memphis Tennessee 38119
Forest Investigative Site 008 Dallas Texas 75235
Forest Investigative Site 007 Middleton Wisconsin 53562

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01254305, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 5, 2014 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01254305 live on ClinicalTrials.gov.

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