drugset / Trial / NCT00888004
Efficacy and Safety of AFQ056 in Reducing L-dopa Induced Dyskinesias in Parkinson's Disease Patients
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This study will evaluate the safety and efficacy of administration of AFQ056 in combination with L-dopa, in reducing the number of L-dopa related dyskinesias in Parkinson's disease patients.
Timeline
- Start
- 2009-03
- Primary completion
- 2009-08
- Completion
- —
Outcome
Mixed primary results
paper AFQ056-treated patients showed significant improvements in dyskinesias on day 16 versus placebo (eg, Lang-Fahn Activities of Daily Living Dyskinesia Scale, P = .021 [study 1] PMID 21484867 ↗
paper No significant changes were seen from baseline on day 16 on the Unified Parkinson's Disease Rating Scale-part III in either study. PMID 21484867 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Mavoglurant | Small molecule | 25 mg | Oral |
| Subject | Mavoglurant | Small molecule | 150 mg | Oral |