Fibromyalgia Clinical Trial
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
The objective of this study is to evaluate the safety, tolerability and efficacy of milnacipran in patients with an inadequate response to duloxetine for the treatment of fibromyalgia.
- Two weeks Duloxetine 60 mg Open-Label Period
- Randomization to Double-Blind Treatment Period: 10 weeks Milnacipran (direct switch) or
10 weeks placebo (one week blinded 30 mg duloxetine)
- One week Double-Blind Down-Taper Period
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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