Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional

ADX48621 for the Treatment of Levodopa Induced Dyskinesia in Patients With Parkinson's Disease

ClinicalTrials.gov ID: NCT01336088

Public ClinicalTrials.gov record NCT01336088. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 4:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group, Multicenter Study to Evaluate the Safety, Tolerability and Efficacy of ADX48621 in the Treatment of Levodopa Induced Dyskinesia in Patients With Parkinson's Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of the study is to evaluate the safety and tolerability of ADX48621 in Parkinson's disease patients following four weeks of dosing. The secondary objectives of the study include the evaluation of the efficacy of ADX48621 compared with placebo in reducing levodopa induced dyskinesia in patients with Parkinson's; the evaluation of the effect of ADX48621 on symptoms of Parkinson's disease and patient ability to function, and the evaluation of the effect of coadministration of ADX48621 on L-dopa efficacy.

Study identification

NCT ID
NCT01336088
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Addex Pharma S.A.
Industry
Enrollment
83 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
30 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2011
Primary completion
Jan 31, 2012
Completion
Jan 31, 2012
Last update posted
Jul 15, 2012

2011 – 2012

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Addex Investigator Site Birmingham Alabama 35233
Addex Investigator Site Phoenix Arizona 85013
Addex Investigator Site La Jolla California 92037
Addex Investigator Site Los Angeles California 90033
Addex Investigator Site Sunnyvale California 94085
Addex Investigator Site New Haven Connecticut 06510
Addex Investigator Site Boca Raton Florida 33612
Addex Investigator Site Tampa Florida 33606
Addex Investigator Site Chicago Illinois 60612
Addex Investigator Site Southfield Michigan 48034
Addex Investigator Site Commack New York 11725
Addex Investigator Site Portland Oregon 97239
Addex Investigator Site Kirkland Washington 98034

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01336088, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 15, 2012 · Synced Sep 6, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01336088 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →