A Phase 2 Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study of TD-9855 in Patients With Fibromyalgia (FM)
TD-9855 Group 1
+ TD-9855 Group 2
+ Placebo
Muscular Diseases+3
+ Musculoskeletal Diseases
+ Nervous System Diseases
Treatment Study
Summary
Study start date: November 1, 2012
Actual date on which the first participant was enrolled.The purpose of this study study is to determine whether TD-9855 is effective in treating patients with fibromyalgia.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.392 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: • American College of Rheumatology (ACR) Diagnostic Criteria for Fibromyalgia (FM) Informed consent 18 to 65 years of age Discontinue therapy with adrenergic-acting drugs, and certain other medications Only acetaminophen or NSAID as rescue pain medication No narcotic pain meds or benzodiazepines Only non-benzodiazepines as rescue hypnotics Exclusion Criteria: Any current psychiatric disorder, lifetime bipolar disorder, severe comorbid Axis II disorder, mental retardation, etc, as assessed by Mini International Neuropsychiatric Interview (MINI) Major depression at screening by MINI when unable to be washed out of MDD meds (investigator or provider's judgment) Risk of suicide (investigator opinion and/or C-SSRS) Recent history of substance or alcohol abuse BMI <18 or ≥45 Concurrent disease; pain for diagnosed illness other than FM; non-compliance; history of seizures; pheochromocytoma; glaucoma; CV disease; orthostatic hypotension or orthostatic tachycardia; untreated sleep apnea Abnormal lab values (liver, kidney, thyroid, and others)
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
33.333% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 34 locations
Rheumatology Associates of North Alabama, PC
Huntsville, United StatesOpen Rheumatology Associates of North Alabama, PC in Google MapsDedicated Clinical Research
Goodyear, United StatesTriWest Research Associates, LLC
El Cajon, United StatesArroyo Medical Group, Inc.
Pismo Beach, United States