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Completed Phase 4 Interventional Results available

Study of Milnacipran in Patients With Inadequate Response to Duloxetine for the Treatment of Fibromyalgia

ClinicalTrials.gov ID: NCT01077375

Public ClinicalTrials.gov record NCT01077375. 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 Jul 22, 2026, 8:21 PM 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 Multicenter, Randomized, Double-Blind, Placebo-Controlled Switch Study to Evaluate the Safety, Tolerability and Efficacy of Milnacipran in Patients With an Inadequate Response to Duloxetine for the Treatment of Fibromyalgia

Study identification

NCT ID
NCT01077375
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Forest Laboratories
Industry
Enrollment
107 participants

Conditions and interventions

Conditions

Interventions

  • Placebo Drug
  • Milnacipran Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 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
Jan 31, 2010
Primary completion
Nov 30, 2010
Completion
Dec 31, 2010
Last update posted
Jan 25, 2012

2010 – 2011

United States locations

U.S. sites
26
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
Forest Investigative Site 013 Sacramento California 95825
Forest Investigative Site 022 Cromwell Connecticut 06416
Forest Investigative Site 021 Danbury Connecticut 06810
Forest Investigative Site 007 Delray Beach Florida 33484
Forest Investigative Site 008 Ocala Florida 34471
Forest Investigative Site 009 Orlando Florida 32806
Forest Investigative Site 016 Orlando Florida 32806
Forest Investigative Site 012 St. Petersburg Florida 33709
Forest Investigative Site 019 Tampa Florida 33614
Forest Investigative Site 006 Atlanta Georgia 30328
Forest Investigative Site 024 Atlanta Georgia 30328
Forest Investigative Site 015 Evansville Indiana 47713
Forest Investigative Site 005 Worchester Massachusetts 01610
Forest Investigative Site 010 Jackson Mississippi 39202
Forest Investigative Site 025 St Louis Missouri 63141
Forest Investigative Site 018 Willingboro New Jersey 08046
Forest Investigative Site 014 Syracuse New York 13210
Forest Investigative Site 023 Charlotte North Carolina 28209
Forest Investigative Site 002 Cincinnati Ohio 45219
Forest Investigative Site 003 Cleveland Ohio 44122
Forest Investigative Site 001 Medford Oregon 97504
Forest Investigative Site 020 Mechanicsburg Pennsylvania 17055
Forest Investigative Site 011 Greer South Carolina 29651
Forest Investigative Site 004 Salt Lake City Utah 84102
Forest Investigative Site 017 Bellevue Washington 98007
Forest Investigative Site 026 Racine Wisconsin 53406

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 NCT01077375, 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 Jan 25, 2012 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01077375 live on ClinicalTrials.gov.

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