Giant Axonal Neuropathy Natural History Study

This study is currently recruiting participants.
Verified November 2012 by Columbia University
Sponsor:
Collaborator:
University of North Carolina, Chapel Hill
Information provided by (Responsible Party):
Douglas M. Sproule, MD MSc, Columbia University
ClinicalTrials.gov Identifier:
NCT01503125
First received: December 29, 2011
Last updated: November 19, 2012
Last verified: November 2012
  Purpose

Giant Axonal Neuropathy (GAN) is a devastating and rare childhood disease. Children with GAN develop increasing muscle weakness, impaired sensation, and at times mental retardation. GAN starts in infancy, leads to significant disability, and typically leads to death within the first 30 years of life. GAN is caused by a defect in the "gigaxonin" (GAN) gene, resulting in pathologically enlarged and dysfunctional nerves. Currently, there is no effective therapy. To find out what medications can help patients with GAN, the investigators have to conduct clinical trials. In this study, the investigators propose to prepare for future clinical trials and will invite GAN patients to join our research effort.

The investigators will examine them regularly to better understand their disease. The visits will include questions, a physical exam, blood drawing, a lumbar puncture, and a skin biopsy. The visits will also include tests that assess the electrical conductivity of the patients' nerves as well as a test to measure the patients' brain wave activity. In addition, the investigators will be performing tests to evaluate the patients' motor function, their vision, and thinking ability. Identifying an effective GAN treatment is very important because there is currently none. Clinical trials are the only way to decide whether a new treatment works in GAN patients or not.

With the future objective of conducting clinical trials in GAN, the proposed project has three specific aims. The first is to plan for clinical trials by developing reliable outcome measures, and establishing the infrastructure needed to carry out efficient clinical trials. The second is to further characterize the patient population from a clinical and molecular point of view, and the third aim is to utilize the information gathered in this study to further pre-clinical GAN drug development to select candidate drugs.


Condition
Giant Axonal Neuropathy

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Clinical Study of Giant Axonal Neuropathy

Resource links provided by NLM:


Further study details as provided by Columbia University:

Primary Outcome Measures:
  • Gross Motor Function Measure (GMFM) [ Time Frame: Up to 24 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Nerve Conduction Study (NCS)/Motor Unit Number Estimation (MUNE) [ Time Frame: Up to 24 months ] [ Designated as safety issue: No ]
  • Somatosensory Evoked Potential (SSEP) [ Time Frame: Up to 24 months ] [ Designated as safety issue: No ]
  • Brainstem Auditory Evoked Response (BAER) [ Time Frame: Up to 24 months ] [ Designated as safety issue: No ]
  • Pulmonary Function Testing (PFT)/Forced Vital Capacity (FVC) [ Time Frame: Up to 24 months ] [ Designated as safety issue: No ]

Biospecimen Retention:   Samples With DNA

Skin Tissue, Blood, Cerebrospinal fluid (CSF)


Estimated Enrollment: 15
Study Start Date: December 2011
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: December 2014 (Final data collection date for primary outcome measure)
  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

People diagnosed with Giant Axonal Neuropathy

Criteria

Inclusion Criteria:

  1. Clinical diagnosis of Giant Axonal Neuropathy.
  2. Documentation of the presence of a mutation in the GAN gene as determined by gene sequencing from a CAP/CLIA certified laboratory or an equivalent organization.
  3. Parents or if applicable subjects must give informed consent must be capable of complying with the study procedures.
  4. Willing and able to comply with all protocol requirements and procedures.

Exclusion Criteria:

  1. Unwilling or unable to travel to Columbia University Medical Center.
  2. Unstable medical condition precluding participation.
  3. Significant respiratory compromise that would interfere with safe travel to site of evaluation.
  4. Having a contraindication to the MRI safety requirements, including pacemaker or other implanted electrical device, brain stimulator, some types of dental implants, aneurysm clips (metal clips on the wall of a large artery), metallic prostheses (including metal pins and rods, heart valves, and cochlear implants), implanted delivery pump, shrapnel fragments, or history of claustrophobia.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01503125

Contacts
Contact: Jonathan D. Marra, M.A. 212-305-2461 jdm2132@columbia.edu

Locations
United States, New York
Columbia University Pediatric Neuromuscular Center Recruiting
New York, New York, United States, 10032
Contact: Jonathan D. Marra, M.A.    212-305-2461    jdm2132@columbia.edu   
Principal Investigator: Douglas M Sproule, MD, MSc         
Sponsors and Collaborators
Columbia University
University of North Carolina, Chapel Hill
Investigators
Principal Investigator: Douglas M. Sproule, MD, MSc Columbia University
  More Information

Additional Information:
No publications provided

Responsible Party: Douglas M. Sproule, MD MSc, Assistant Professor of Neurology, Pediatrics, Columbia University
ClinicalTrials.gov Identifier: NCT01503125     History of Changes
Other Study ID Numbers: AAAI4500
Study First Received: December 29, 2011
Last Updated: November 19, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by Columbia University:
GAN
Giant Axonal Neuropathy
Neuromuscular Disease
Natural History Study
Observational Study

Additional relevant MeSH terms:
Nervous System Malformations
Demyelinating Diseases
Polyneuropathies
Nerve Compression Syndromes
Neurologic Manifestations
Neurotoxicity Syndromes
Giant Axonal Neuropathy
Nervous System Diseases
Peripheral Nervous System Diseases
Neuromuscular Diseases
Signs and Symptoms
Poisoning
Substance-Related Disorders
Hereditary Sensory and Motor Neuropathy
Heredodegenerative Disorders, Nervous System
Neurodegenerative Diseases
Congenital Abnormalities
Genetic Diseases, Inborn

ClinicalTrials.gov processed this record on April 22, 2014