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Safety and Efficacy of AVP-923 in the Treatment of Levodopa-induced Dyskinesia in Parkinson's Disease Patients — LID in PD  

Parkinson's Disease Clinical Trial

Official title:
A Phase 2a, Double-blind, Randomized, Placebo-controlled, Crossover Study to Evaluate the Safety and Efficacy of AVP-923 (Dextromethorphan/Quinidine) in the Treatment of Levodopa-induced Dyskinesia in Parkinson's Disease Patients.

Clinical Trial Summary

To evaluate the efficacy, safety, and tolerability of AVP-923 capsules containing 45 mg dextromethorphan and 10 mg quinidine (AVP-923-45) compared to placebo for the treatment of levodopa-induced dyskinesia (LID) in patients with Parkinson's disease (PD).

Clinical Trial Description

Proof-of-concept phase 2a, double-blind, randomized, placebo-controlled, crossover study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01767129
Study type Interventional
Source Avanir Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date October 16, 2013
Completion date February 5, 2015
View Details
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