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

Primary Purpose

Parkinson's Disease

Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
VY-AADC02
Sham (Placebo) Surgery
Sponsored by
Neurocrine Biosciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson's Disease focused on measuring Parkinson's Disease (PD), Aromatic L-Amino Acid Decarboxylase, AADC, AAV, VY-AADC02, AAV2-hAADC, DDC, Gene Therapy, Levodopa, Dopamine, Neurosurgery, NBIb-1817, Motor Fluctuations

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Key Inclusion Criteria:

  1. Males and females, 40 to 75 years of age (inclusive)
  2. Diagnosis of PD, consistent with United Kingdom Brain Bank Criteria
  3. Motor responsiveness to dopaminergic therapy, demonstrated by improvement in MDS-UPDRS III score
  4. Disease duration from diagnosis of ≥4 years
  5. An average of ≥3 hours of OFF time (ie, periods of insufficient control of motor PD symptoms) per day over 3 consecutive days as confirmed by the PD Diary
  6. 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
  7. In the judgment of the Investigator, stable Parkinson's features and symptoms for at least 4 weeks prior to screening evaluation
  8. 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
  9. Ability to travel to study visits

Key Exclusion Criteria:

  1. 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
  2. MoCA score <26
  3. New or unstable psychiatric conditions (psychosis, depression) within 1 year of screening
  4. Brain imaging abnormalities in the striatum or other regions that would substantially increase risk of surgery
  5. Contraindication to MRI and/or gadolinium-based contrast agents
  6. 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
  7. History of malignancy other than treated carcinoma in situ within 3 years of screening evaluation
  8. 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
  9. Severe, biphasic and/or uncontrolled dyskinesia
  10. Disabling or uncontrolled impulse control disorders

Sites / Locations

  • UC Irvine
  • UC Davis Health System
  • San Francisco VA Medical Center
  • University of California, San Francisco
  • University of Colorado
  • Emory University Hospital
  • Northwestern Medical Faculty Foundation
  • University of Kansas Medical Center
  • Tufts Medical Center
  • Beth Israel Deaconess Medical Center (BIDMC)
  • University of Michigan
  • Michigan State University Department of Neurology
  • Hackensack University Medical Center
  • NYU Langone Medical Center
  • Cleveland Clinic-Center for Neurological Restoration
  • Ohio State University Clinical Trials Management Office
  • The Hospital of the University of Pennsylvania
  • Thomas Jefferson University Hospital
  • University of Philadelphia, Dept of Neurology
  • University of Pittsburgh Medical Center (UPMC)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

VY-AADC02 (NBIb-1817)

Sham (Placebo) Surgery

Arm Description

Single administration of up to 3.6 x 10^12 vector genomes (vg) of VY-AADC02

Sham surgical procedure

Outcomes

Primary Outcome Measures

Change in ON time without troublesome dyskinesia as recorded by participant in Parkinson's Disease (PD) diary

Secondary Outcome Measures

Change in Movement Disorder Society - Unified Parkinson's Disease Rating Scale (MDS-UPDRS) III score in the OFF state
Change in MDS-UPDRS II score

Full Information

First Posted
May 16, 2018
Last Updated
March 19, 2023
Sponsor
Neurocrine Biosciences
Collaborators
Voyager Therapeutics
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1. Study Identification

Unique Protocol Identification Number
NCT03562494
Brief Title
VY-AADC02 for Parkinson's Disease With Motor Fluctuations (RESTORE-1)
Official Title
A Randomized, Sham Surgery Controlled, Double-blind, Multi-center, Phase 2 Clinical Trial, Evaluating the Efficacy and Safety of VY-AADC02 in Moderate to Advanced Parkinson's Disease Patients With Motor Fluctuations
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 17, 2018 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Neurocrine Biosciences
Collaborators
Voyager Therapeutics

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objectives of this study are to assess the efficacy, safety and tolerability of VY-AADC02 in Patients with Parkinson's Disease with Motor Fluctuations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson's Disease
Keywords
Parkinson's Disease (PD), Aromatic L-Amino Acid Decarboxylase, AADC, AAV, VY-AADC02, AAV2-hAADC, DDC, Gene Therapy, Levodopa, Dopamine, Neurosurgery, NBIb-1817, Motor Fluctuations

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Randomized, Sham Surgery Controlled, Double-blind, Multi-center
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
85 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
VY-AADC02 (NBIb-1817)
Arm Type
Experimental
Arm Description
Single administration of up to 3.6 x 10^12 vector genomes (vg) of VY-AADC02
Arm Title
Sham (Placebo) Surgery
Arm Type
Placebo Comparator
Arm Description
Sham surgical procedure
Intervention Type
Biological
Intervention Name(s)
VY-AADC02
Intervention Description
Adeno-associated viral vector serotype 2 encoding human aromatic L-amino acid decarboxylase (AAV2- hAADC) infusion into the brain
Intervention Type
Other
Intervention Name(s)
Sham (Placebo) Surgery
Intervention Description
Bilateral partial burr/twist holes without dura penetration
Primary Outcome Measure Information:
Title
Change in ON time without troublesome dyskinesia as recorded by participant in Parkinson's Disease (PD) diary
Time Frame
Baseline to Day 360
Secondary Outcome Measure Information:
Title
Change in Movement Disorder Society - Unified Parkinson's Disease Rating Scale (MDS-UPDRS) III score in the OFF state
Time Frame
Baseline to Day 360
Title
Change in MDS-UPDRS II score
Time Frame
Baseline to Day 360
Other Pre-specified Outcome Measures:
Title
Safety outcome measured by treatment emergent adverse events (TEAEs), serious adverse events (SAEs), changes in vital signs and clinical laboratory analysis, and immunogenicity
Time Frame
Baseline to Day 360

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria: 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 MDS-UPDRS III score Disease duration from diagnosis of ≥4 years An average of ≥3 hours of OFF time (ie, 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 Key Exclusion Criteria: 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 MoCA score <26 New or unstable psychiatric conditions (psychosis, depression) within 1 year of screening Brain imaging abnormalities in the striatum or other regions that would substantially increase risk of surgery Contraindication to MRI and/or gadolinium-based contrast agents 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 History of malignancy other than treated carcinoma in situ within 3 years of screening evaluation 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 Severe, biphasic and/or uncontrolled dyskinesia Disabling or uncontrolled impulse control disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clinical Development Lead
Organizational Affiliation
Neurocrocrine Biosciences
Official's Role
Study Director
Facility Information:
Facility Name
UC Irvine
City
Irvine
State/Province
California
ZIP/Postal Code
92697
Country
United States
Facility Name
UC Davis Health System
City
Sacramento
State/Province
California
ZIP/Postal Code
95817
Country
United States
Facility Name
San Francisco VA Medical Center
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
University of Colorado
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Facility Name
Emory University Hospital
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
Northwestern Medical Faculty Foundation
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
University of Kansas Medical Center
City
Kansas City
State/Province
Kansas
ZIP/Postal Code
66160
Country
United States
Facility Name
Tufts Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Facility Name
Beth Israel Deaconess Medical Center (BIDMC)
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Facility Name
Michigan State University Department of Neurology
City
East Lansing
State/Province
Michigan
ZIP/Postal Code
48824
Country
United States
Facility Name
Hackensack University Medical Center
City
Hackensack
State/Province
New Jersey
ZIP/Postal Code
07601
Country
United States
Facility Name
NYU Langone Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10017
Country
United States
Facility Name
Cleveland Clinic-Center for Neurological Restoration
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Facility Name
Ohio State University Clinical Trials Management Office
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
The Hospital of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Thomas Jefferson University Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
University of Philadelphia, Dept of Neurology
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
University of Pittsburgh Medical Center (UPMC)
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31127735
Citation
McFarthing K, Prakash N, Simuni T. CLINICAL TRIAL HIGHLIGHTS: 1. GENE THERAPY FOR PARKINSON'S, 2. PHASE 3 STUDY IN FOCUS - INTEC PHARMA'S ACCORDION PILL, 3. CLINICAL TRIALS RESOURCES. J Parkinsons Dis. 2019;9(2):251-264. doi: 10.3233/JPD-199001. No abstract available.
Results Reference
derived

Learn more about this trial

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

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