Study of the Effect of SR57667B on 18F-Dopa PET Imaging in Patients With Parkinson's Disease

Sanofi

Status and phase

Completed

Phase 2

Conditions

Parkinson Disease

Treatments

Drug: SR57667B

Study type

Interventional

Funder types

Industry

Identifiers

NCT00220272

ACT5288

Details and patient eligibility

About

The primary objective is to study the effect of SR57667B at the dose of 4 mg/d on progression of dopaminergic nigro-striatal lesions assessed by 18F-Dopa PET imaging.
Secondary objectives are to assess the effect of SR57667B on symptomatic decline in patients with early PD, to assess the safety/tolerability of SR57667B in patients with early PD and to document plasma concentrations of SR57667 in patients with early PD.

Full description

Multinational, multicenter, randomized, parallel-group, double-blind, phase II study.Randomization stratified on the dopaminergic treatment, in two strata: treatment by levodopa or dopamine agonist.

Enrollment

183 patients

Sex

All

Ages

35+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female outpatients.
Age >=35 years at screening.
Diagnosis of Parkinson's syndrome, on at least two of the three key Parkinson's symptoms, i.e. resting tremor, bradykinesia and rigidity.
Duration of the disease of less than 3 years since diagnosis.
Modified Hoehn and Yahr stage <= 2.5.
Patient optimized on monotherapy by levodopa or a dopamine agonist·
Generally healthy and ambulatory.
Patient has given his informed written consent and is capable of following study procedures.

Exclusion criteria

Any indication of forms of parkinsonism other than PD.
Severe resting tremor. Presence of either dyskinesia, fluctuations, or loss of postural reflexes·
Treatment with amantadine, anticholinergics, catechol-o-methyltransferase (COMT ) inhibitors, selegiline, dopamine receptor antagonists, catecholamine depleters, indirect dopamine agonists or alphamethyldopa. Electroconvulsive therapy (ECT).Use of CYP3A4 strong, and moderate inducers or inhibitors. Participation in another clinical trial with an investigational drug within two months prior to randomization.
Dementia, uncontrolled depression, psychotic disorder. History of substance-related disorders including alcohol or other substance use disorders.
Females of child bearing potential.
Evidence (detected by history, physical examination and/or laboratory/ECG tests) of any clinically significant or unstable medical disorder that could interfere with the patient's participation in the clinical trial; interfere with the absorption, metabolism or excretion of the study medication; or interfere with the evaluation of the study drug. Alterations of laboratory tests or ECG findings of potential clinical significance.