drugset / Trial / NCT00888004

Efficacy and Safety of AFQ056 in Reducing L-dopa Induced Dyskinesias in Parkinson's Disease Patients

NCT00888004 ↗

Phase 2 Completed 28 enrolled Novartis
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

EvaluationDrugModalityDoseRoute
Subject Mavoglurant Small molecule 25 mg Oral
Subject Mavoglurant Small molecule 150 mg Oral