Clinical Trials Directory

Trials / Terminated

TerminatedNCT02153645

Efficacy and Safety of Amantadine Hydrochloride (HCl) ER Tablets to Treat Parkinson's Disease Patients With LID.

A Multicenter, Randomized, Placebo-controlled, Double-blind, 16 Week Study to Evaluate the Efficacy and Safety of Amantadine HCl Extended Release Tablets in Parkinson's Disease Subjects With Levodopa-Induced Dyskinesias

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
87 (actual)
Sponsor
Adamas Pharmaceuticals, Inc. · Industry
Sex
All
Age
30 Years – 85 Years
Healthy volunteers
Not accepted

Summary

This study was terminated early due to slow enrollment with 87 of 162 planned subjects enrolled. The purpose of this multi-center, randomized, double-blind, parallel-group, 16 week study is to compare the efficacy and safety of two different dose levels of Amantadine Extended Release Tablets to placebo for the treatment of levodopa induced dyskinesia in patients with Parkinson's disease.

Detailed description

This study was terminated early due to slow enrollment with 87 of 162 planned subjects enrolled. Amantadine has been used for many years as a treatment for Parkinson's disease. It has been reported in the literature to effectively treat the motor complications of levodopa, especially dyskinesia, but it must be given 2 to 4 times a day. The purpose of this multi-center, randomized, double-blind, parallel-group, 16 week study is to compare the efficacy and safety of two different dose levels of Amantadine Extended Release Tablets to placebo for the treatment of levodopa induced dyskinesia in patients with Parkinson's disease. The dose will be given once a day in the morning so that amantadine concentrations are maintained throughout the day for treating the levodopa induced dyskinesia, but will be lower during the night, potentially reducing the negative impact of amantadine on sleep.

Conditions

Interventions

TypeNameDescription
DRUG240mg Amantadine HCl ER tablets
DRUGPlacebo tablets
DRUG320mg Amantadine HCl ER tablets

Timeline

Start date
2014-08-18
Primary completion
2016-05-20
Completion
2016-05-20
First posted
2014-06-03
Last updated
2022-02-16
Results posted
2019-04-02

Locations

56 sites across 5 countries: United States, Canada, France, Germany, Spain

Source: ClinicalTrials.gov record NCT02153645. Inclusion in this directory is not an endorsement.