Clinical Trials Directory

Trials / Completed

CompletedNCT02136914

ADS-5102 for the Treatment of Levodopa Induced Dyskinesia (EASE LID Study)

Efficacy and Safety of ADS-5102 (Amantadine HCl) Extended Release Capsules for the Treatment of Levodopa Induced Dyskinesia in Parkinson's Disease Patients (EASE LID Study)

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

Summary

This is a multi-center, randomized, double-blind, placebo-controlled, 2-arm, parallel group study to evaluate the efficacy and safety of ADS-5102 extended release (ER) capsules, an investigational formulation of amantadine, dosed once nightly at bedtime for the treatment of levodopa induced dyskinesia (LID) in subjects with Parkinson's disease (PD). The novel pharmacokinetic profile of ADS-5102 is expected to achieve i) maximal concentrations in the early morning through mid-day, when LID can be troublesome, and ii) lower concentrations in the evening, potentially reducing the negative impact of amantadine on sleep. This pharmacokinetic profile could enable higher doses to be tolerated with a once-nightly ER formulation than can be tolerated with an immediate-release formulation. The once-nightly dosing regimen may also provide enhanced convenience and compliance. In a previous clinical study, ADS-5102 met its primary endpoint; LID was significantly reduced as measured by the change in UDysRS score over 8 weeks vs. placebo.

Conditions

Interventions

TypeNameDescription
DRUGADS-5102Oral capsules to be administered once nightly at bedtime, for 25 weeks
OTHERPlaceboOral capsules to be administered once nightly at bedtime, for 25 weeks

Timeline

Start date
2014-05-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2014-05-13
Last updated
2018-02-06
Results posted
2018-02-06

Locations

46 sites across 2 countries: United States, Canada

Source: ClinicalTrials.gov record NCT02136914. Inclusion in this directory is not an endorsement.