drugset / Trial / NCT00511940
Acamprosate in the Treatment of Binge-Eating Disorder
Phase 2/3
Completed
40 enrolled
Lindner Center of HOPE
Forest Laboratories · collabUniversity of Cincinnati · collab
RandomizedParallel-groupTriple-blindTreatment
Summary
The purpose of this research study is to determine the efficacy (how well it works), tolerability and safety of acomprosate compared with placebo in patients with binge eating disorder.
Timeline
- Start
- 2007-04
- Primary completion
- 2011-01
- Completion
- 2011-01
Outcome
Missed primary endpoint
paper acamprosate was not associated with a significantly greater rate of reduction in binge eating episode frequency or any other measure in the primary longitudinal analysis PMID 21080416 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Acamprosate | Small molecule | 999 mg | Oral |
| Subject | Acamprosate | Small molecule | 2997 mg | Oral |