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

NCT00986414 ↗

Phase 2 Completed 260 enrolled Novartis
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

EvaluationDrugModalityDoseRoute
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 —