drugset / Trial / NCT00986414
Evaluation of the Efficacy and Safety of AFQ056 in Reducing Moderate to Severe L-dopa Induced Dyskinesias in Patients With Parkinson's Disease
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This phase IIb study is designed to determine the safe and efficacious dose or dose range of AFQ056 for the treatment of patients with moderate to severe Parkinson's disease with L-Dopa induced dyskinesias.
Timeline
- Start
- 2009-09
- Primary completion
- 2010-12
- Completion
- —
Outcome
Met primary endpoint
paper demonstrated significant improvements at Week 12 on the modified Abnormal Involuntary Movements Scale compared with placebo PMID 23853029 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Mavoglurant | Small molecule | 10 mg | — |
| Subject | Mavoglurant | Small molecule | 25 mg | — |
| Subject | Mavoglurant | Small molecule | 50 mg | — |
| Subject | Mavoglurant | Small molecule | 75 mg | — |
| Subject | Mavoglurant | Small molecule | 100 mg | — |