Safety and Efficacy of AGN 203818 for Pain Associated With Fibromyalgia Syndrome
Stopped early · Phase 2 · Has a placebo group
Conditions studied: Fibromyalgia
In brief
This study will explore the safety and effectiveness of different doses of AGN 203818 in treating the pain associated with fibromyalgia syndrome. The study is being conducted in 2 parts. Part A enrolled 211 pts dosed with either 3, 20, 60 mg BID AGN 203818 or placebo over 4 week treatment duration. Part B will enroll 440 pts and dose with either 20, 100, 160 mg BID AGN 203818 or placebo over 12 week treatment duration.
Key facts
- Study ID
- NCT00445705
- Run by
- Allergan
- People needed
- 211
- Starts
- 2007-03-01
- Expected to finish
- 2008-01-01
- Last updated by the study team
- 2015-09-07
Who can join
Age: 18 and older, up to 75. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of fibromyalgia syndrome
- Moderate or severe pain associated with fibromyalgia
You may not qualify if…
- Any other uncontrolled disease
- Pregnant or nursing females
Where it is running
- Study site — Canton, Ohio, United States
- Study site — Geneva, Switzerland
- Study site — Stanmore, United Kingdom
Full record on ClinicalTrials.gov
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