Natural History Study in Huntington Disease Gene Expansion Carriers (HDGECs) - SHIELD HD

NCT ID: NCT04406636

Last Updated: 2022-09-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

70 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-19

Study Completion Date

2023-04-30

Brief Summary

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SHIELD HD is an international, multisite, prospective, longitudinal cohort natural history study to assess the natural history of HD and its biomarkers that are associated with modulation of the number of cytosine-adenine-guanine (CAG) repeats in the mutant Huntingtin (HTT) gene.

Approximately 60 patients will be enrolled into the study and followed for up to 24 months at clinical sites in North America and Europe.

The results of this study will inform assessments for a future interventional treatment trial.

Detailed Description

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The rationale for this study is to obtain longitudinal information related to Somatic Instability and DNA damage response genes in HDGECs at various stages of the disease. Established assessments of disease progression will also be recorded.

Conditions

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Huntington Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

Patients who meet all of the following criteria will be eligible to participate in the study:

1. Capacity to comprehend the study objectives and procedures
2. Documentation of genetically confirmed disease by direct DNA testing, defined as a CAG repeat length ≥39 in the HTT gene
3. Ability to undergo and tolerate MRI scans
4. Ability to tolerate blood draws and lumbar punctures

Exclusion Criteria

Patients who meet any of the following criteria will be excluded from participation in the study:

1. Any conditions, including severe chorea and dementia, that would prevent either writing or performing pen and paper, tablet, or computer based tasks as determined by the Investigator
2. Treatment with an investigational drug within 30 days prior to screening or within 5 half lives of the investigational drug, whichever is longer
3. History of gene therapy or cell transplantation or any other experimental brain surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

63 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medpace, Inc.

INDUSTRY

Sponsor Role collaborator

CHDI Foundation, Inc.

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Anne Rosser, PhD FRCP

Role: PRINCIPAL_INVESTIGATOR

Cardiff University

Locations

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University of California, San Diego (UCSD)

San Diego, California, United States

Site Status

Rocky Mountain Movement Disorders Center

Englewood, Colorado, United States

Site Status

Beth Israel Deaconess

Boston, Massachusetts, United States

Site Status

Columbia University

New York, New York, United States

Site Status

Inland Northwest Research

Spokane, Washington, United States

Site Status

Centre for Movement Disorders

Toronto, Ontario, Canada

Site Status

North York General Hospital

Toronto, Ontario, Canada

Site Status

ICM - Institut du Cerveau et de la Moelle épinière

Paris, , France

Site Status

George-Huntington-Institut (GHI)

Münster, , Germany

Site Status

University College London - Institute of Neurology & The National Hospital for Neurology and Neurosurgery

London, , United Kingdom

Site Status

Countries

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United States Canada France Germany United Kingdom

Other Identifiers

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TTX N1

Identifier Type: -

Identifier Source: org_study_id

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