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NCT03562494CompletedPhase 1

VY-AADC02 for Parkinson's Disease With Motor Fluctuations (RESTORE-1)

A Randomized, Sham Surgery Controlled, Double-blind, Multi-center, Phase 1 Clinical Trial, Evaluating the Safety of VY-AADC02 in Moderate to Advanced Parkinson's Disease Patients With Motor Fluctuations

Source: ClinicalTrials.gov · Last updated 10 Dec 2024

Brief summary (registry, in English)

The objective of this study is to assess the safety of VY-AADC02 in participants with Parkinson's disease (PD) with motor fluctuations.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
14 (actual)
First submitted
16 May 2018
Start date
17 Oct 2018
Primary completion date
30 Oct 2024
Lead sponsor
Neurocrine Biosciences
NCT number
NCT03562494

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 14
  • From 17 Oct 2018 to the primary completion date, 30 Oct 2024
  • 11 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Brain imaging abnormalities in the striatum or other regions that would substantially increase risk of surgery
  • Prior brain surgery, infusion therapies or planned treatments that could complicate the study procedure or negatively impact study evaluations as determined from participant interview, screening MRI, or medical records
  • Prior gene transfer, current treatment with any investigational agent (drug or device) within 2 months of screening evaluation, or participation or plans to participate in another research study

Other illness

  • Atypical or secondary parkinsonism, including but not limited to symptoms believed to be due to trauma, brain tumor, infection, cerebrovascular disease, other neurological disease, or to drugs, chemicals, or toxins, as determined by the Investigator
  • New or unstable psychiatric conditions (psychosis, depression) within 1 year of screening
  • History of malignancy other than treated carcinoma in situ within 3 years of screening evaluation
  • Disabling or uncontrolled impulse control disorders

Other

  • Montreal Cognitive Assessment (MoCA) score \<26
  • Contraindication to magnetic resonance imaging (MRI) and/or gadolinium-based contrast agents
  • Severe, biphasic and/or uncontrolled dyskinesia

Who the study is looking for

  • Males and females, 40 to 75 years of age (inclusive)
  • Diagnosis of PD, consistent with United Kingdom Brain Bank Criteria
  • Motor responsiveness to dopaminergic therapy, demonstrated by improvement in Movement Disorder Society - Unified Parkinson's Disease Rating Scale (MDS-UPDRS III score)
  • Disease duration from diagnosis of ≥4 years
  • An average of ≥3 hours of OFF time (that is, periods of insufficient control of motor PD symptoms) per day over 3 consecutive days as confirmed by the PD Diary
  • A stable, optimal regimen of Parkinson's medications including levodopa for at least weeks prior to screening evaluation. Participants must have a minimum duration of levodopa treatment of ≥1 year
  • In the judgment of the Investigator, stable Parkinson's features and symptoms for at least 4 weeks prior to screening evaluation
  • Agrees to defer any elective neurological surgery, including deep brain stimulation or ablation procedure for PD, levodopa or apomorphine infusion, or the addition of new dopaminergic formulations until after the study is completed, if medically appropriate
  • Ability to travel to study visits

Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (11)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emory University Hospital
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
University of Colorado
Coordinator of this site? Confirm its status
AuroraUnited StatesUnknown status
Northwestern Medical Faculty Foundation
Coordinator of this site? Confirm its status
ChicagoUnited StatesUnknown status
Ohio State University Clinical Trials Management Office
Coordinator of this site? Confirm its status
ColumbusUnited StatesUnknown status
UC Irvine
Coordinator of this site? Confirm its status
IrvineUnited StatesUnknown status
University of Kansas Medical Center
Coordinator of this site? Confirm its status
Kansas CityUnited StatesUnknown status
NYU Langone Medical Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
University of Philadelphia, Dept of Neurology
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
University of Pittsburgh Medical Center (UPMC)
Coordinator of this site? Confirm its status
PittsburghUnited StatesUnknown status
UC Davis Health System
Coordinator of this site? Confirm its status
SacramentoUnited StatesUnknown status
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.