Safety and Efficacy of Milnacipran in Pediatric Patients With Primary Fibromyalgia



Status:Terminated
Conditions:Fibromyalgia, Pain
Therapuetic Areas:Musculoskeletal, Rheumatology
Healthy:No
Age Range:13 - 17
Updated:10/14/2017
Start Date:April 2011
End Date:August 2012

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A Multicenter, Randomized, Double-blind, Placebo-Controlled Withdrawal Study to Evaluate the Safety, Tolerability, and Efficacy of Milnacipran in Pediatric Patients With Primary Fibromyalgia

The purpose of this study is to evaluate the safety, tolerability, efficacy, and
pharmacokinetics of milnacipran in pediatric patients aged 13 to 17 years with primary
fibromyalgia.

- 8 weeks open-label milnacipran period

- Followed by randomization to 8-weeks double blind treatment period for eligible patients

Inclusion Criteria:

- Diagnosis of primary fibromyalgia

- 13-17 years of age

Exclusion Criteria:

- Severe psychiatric illness

- Severe renal impairment

- Evidence of active liver disease

- Pregnant or breastfeeding

- Significant risk of suicidality

- Unable, unwilling or unadvisable to discontinue prohibited medications
We found this trial at
30
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Stevensville, Michigan 49127
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Akron, Ohio 44313
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Ann Arbor, Michigan 48106
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Birmingham, Alabama 35216
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Blue Ridge, Georgia 30513
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Cincinnati, Ohio 45219
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Clinton, Utah 84015
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Colorado Springs, Colorado 80909
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Cromwell, Connecticut 06416
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Dayton, Ohio 45406
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Fresno, California 93726
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Greer, South Carolina 29651
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Louisville, Kentucky 40213
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Mechanicsburg, Pennsylvania 17055
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Oklahoma City, Oklahoma 73116
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Orange, California 92868
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Orange City, Florida 32763
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Orlando, Florida 32806
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Peoria, Illinois 61606
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Philadelphia, Pennsylvania 19139
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Racine, Wisconsin 53406
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Raleigh, North Carolina 27607
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Sacramento, California 95817
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Salt Lake City, Utah 84124
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San Antonio, Texas 78229
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Savannah, Georgia 31419
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4664 Commercial Way
Spring Hill, Florida 34609
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West Palm Beach, Florida 33407
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Whitehouse Station, New Jersey 08889
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Winston-Salem, North Carolina 27103
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