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Intrathecal Administration of scAAV9/JeT-GAN for the Treatment of Giant Axonal Neuropathy

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02362438
Recruitment Status : Recruiting
First Posted : February 13, 2015
Last Update Posted : May 27, 2022
Sponsor:
Information provided by (Responsible Party):
National Institutes of Health Clinical Center (CC) ( National Institute of Neurological Disorders and Stroke (NINDS) )

Brief Summary:

Title: Intrathecal Administration of scAAV9/JeT-GAN for the Treatment of Giant Axonal Neuropathy

Background:

- The Gigaxonin gene lets the body make a protein chemical called Gigaxonin. Nerves need Gigaxonin to work properly. Giant Axonal Neuropathy (GAN) causes a shortage of functional Gigaxonin. Nerves stop working normally in people with GAN. This causes problems with walking and sometimes with eating, breathing, and many other activities. GAN has no cure. Over time, GAN can shorten a person s life. Researchers want to see if a gene transfer treatment may help people with GAN.

Objectives:

- To see if a gene transfer is safe and shows potential to help people with GAN.

Eligibility:

- People age 3 and older with GAN.

Design:

  • For 1 month following gene transfer participants must live full-time within 100 miles of the NIH.
  • Participants will be screened by phone and in person. They will take many tests. Some are listed below. Their medical records will be reviewed. Their caregivers may be contacted.
  • Participants will have a total of about 27 visits, weekly, monthly, and then yearly over 15 years. They will include many of the tests below.
  • Physical and nervous system exams.
  • Blood, urine, and stool samples.
  • Nerve, lung, heart, and eye tests.
  • Questionnaires.
  • MRI scans, nerve biopsies, and spinal taps. Participants will be sedated for some tests.
  • Speech, memory, muscle, and mobility tests.
  • Skin biopsy (small sample removed).
  • Participants will take many medicines. Some require intravenous lines.
  • Participants will get the gene transfer through an injection by spinal tap into their cerebrospinal fluid, which flows around the brain and spinal cord. The genes are packed in a modified virus that carries the genes to cells in their body. Participants safety is not guaranteed.

Condition or disease Intervention/treatment Phase
Giant Axonal Neuropathy Gene Transfer Genetic: scAAv9/JeT-GAN Phase 1

Detailed Description:

This is an open-label and non-randomized first-in-human (Phase 1) clinical trial which incorporates an escalating single dose paradigm to assess safety of the gene transfer vector scAAV9/JeT-GAN administered intrathecally to target the brain and spinal cord of individuals with genetically confirmed Giant Axonal Neuropathy.

GAN is a chronic neurodegenerative autosomal recessive disease pathologically characterized by enlarged axons with disordered intermediate filaments and microtubules. The disease pathology is due to loss-of-function variants in the GAN gene, which encodes the protein gigaxonin. Gigaxonin plays a major role in the maintenance of orderly and functional intermediate filament (IF) architecture, which is critical for axonal function. Onset of symptoms, usually at three to four years of age, generally manifests with a clumsy and unsteady gait (sensory ataxia). In the peripheral nervous system, the disease progressively affects predominantly sensory and motor nerves. By the end of the second decade of life, patients typically are wheelchair dependent with limited use of the arms and little to no use of their legs. During the second decade a tracheostomy or other means of ventilation, as well as a feeding tube, are often necessary. Death normally occurs in the second or third decade of life. We recently identified a sub-cohort of patients with a milder and later onset, yet progressive form of GAN characterized by a prolonged preservation of ambulation and less extensive white matter changes on brain MRI restricted to the infratentorial regions. These individuals are good trial candidates given the increased prospect of benefit at milder disease stages. There are no statistics on the incidence of GAN, but it is considered extremely rare and does not have an approved treatment aside from supportive care. Intrathecal delivery of a gene transfer vector carrying a normal copy of the GAN to the spinal cord and brain offers a potentially effective treatment for GAN.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 21 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase I Study of Intrathecal Administration of scAAV9/JeT-GAN for the Treatment of Giant Axonal Neuropathy
Actual Study Start Date : April 24, 2015
Estimated Primary Completion Date : June 30, 2022
Estimated Study Completion Date : April 1, 2030


Arm Intervention/treatment
Experimental: 10X
Highest dose in the escalation scheme
Genetic: scAAv9/JeT-GAN
scAAV9/JeT-GAN is a biological gene transfer reagent

Experimental: 1X
Lowest dose in the escalation scheme
Genetic: scAAv9/JeT-GAN
scAAV9/JeT-GAN is a biological gene transfer reagent

Experimental: 3.3X
2nd dose increase in escalation scheme
Genetic: scAAv9/JeT-GAN
scAAV9/JeT-GAN is a biological gene transfer reagent

Experimental: 5X
3rd dose increase in escalation scheme
Genetic: scAAv9/JeT-GAN
scAAV9/JeT-GAN is a biological gene transfer reagent




Primary Outcome Measures :
  1. To assess the safety of the vector [ Time Frame: 12 months ]
    Adverse event reports will be used to assess safety


Secondary Outcome Measures :
  1. Assessment of motor and sensory disease symptoms compare to baseline [ Time Frame: 12 months ]
    Physical therapy assessments will be used for motor symptoms. Nerve conduction studies will be used to assess sensory symptoms.

  2. Examination of neuropathology in peripheral nerve biopsies following treatment [ Time Frame: 12 months ]
    Nerve biopsies will be collected and analyzed to examine neuropathology.

  3. Examination of cerebrospinal fluid following treatment [ Time Frame: 12 months ]
    CSF will be collected via lumbar puncture and analyzed to monitor for inflammatory markers.

  4. Assessment of vector shedding following treatment [ Time Frame: 12 months ]
    Biospecimens will be collected to analyze vector shedding.

  5. Determine safety and tolerability of gene transfer in patients with null mutations receiving immunosuppression [ Time Frame: 12 months ]
    Adverse event reporting will be used to assess the safety of gene transfer in CRIM-negative patients.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   3 Years to 99 Years   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria
  • INCLUSION CRITERIA:

To participate in this study, subjects must meet the following criteria:

  • Age 3 years or older.
  • Genetic diagnosis of GAN: Identified pathogenic variant(s) on both copies of the GAN gene. If the variants found are not previously reported, then predictive software tools will be utilized to determine the degree of certainty that the variant is expected to be pathogenic (disease causing). This will also be evaluated in the context of the clinical and pathological phenotype.
  • Men capable of fathering a child must agree to use barrier contraception (combination of a condom and spermicide) or limit activity to post-menopausal, surgically sterilized, or contraception-practicing partners, for 6 months after administration of investigational product. Women and girls of childbearing potential (and parents/ guardians for minors < 18) must agree to have urine human chorionic gonadotropin testing performed to rule out the possibility of pregnancy at each visit. Those women who are sexually active must also agree to use barrier contraception as well or limit activity to surgically sterilized or contraception-practicing partners for 3-6 months after the administration of the investigational product. This limitation is set because of the unknown risk associated with the administration of this vector genome to offspring. There is no known risk of sexual transmission of the vector.
  • Willing and able to give informed consent if >17 years of age and assent if >7 years of age. For patients ages 7-17, parents or legal guardians must also consent to the child s participation in the study. Adults who lack capacity to consent but who have an appropriate surrogate may be included.
  • Willingness to undergo a nerve biopsy at baseline and at 12 months after treatment.
  • Agree to reside within 100 miles of the study site for at least 4 weeks following treatment (may include housing on NIH campus).

EXCLUSION/DEFERRAL CRITERIA:

To participate in this study, a patient MUST NOT have the following characteristics:

  • Pregnant or lactating patients
  • Forced vital capacity <= 50% of predicted value (if patient is >/= 5 years old; otherwise, baseline FVC is not required in those < 5 years old at time of enrollment)
  • Ventilator dependence to include daytime use of assisted ventilation
  • Current clinically significant infections including any requiring systemic treatment including but not limited to Human immunodeficiency virus, Hepatitis A, B, or C, Varicella zoster virus, or HTLV-1
  • Prior history of bacterial meningitis
  • Unwilling to undergo lumbar puncture at baseline and up to 2 to 3 times during follow up during the first year after treatment.
  • Clinically significant echocardiogram abnormality per PI, anesthesiologist, and cardiologist
  • Clinically significant electrocardiogram (ECG) abnormality per PI, anesthesiologist, and cardiologist
  • History of brain or spinal cord disease that would interfere with the LP procedures, CSF circulation, or safety assessments
  • Presence of an implanted shunt for the drainage of CSF or an implanted CNS catheter
  • Any prior participation in a study in which a gene therapy vector or stem cell transplantation was administered to avoid any ambiguity in the safety assessment resulting from lingering effects from a previous treatment.
  • Participation in an IND, IDE, or equivalent clinical study in the past six months.
  • History of or current chemotherapy, radiotherapy or other immunosuppressive therapy within the past 30 days. Corticosteroid treatment may be permitted at the discretion of the PI.
  • Immunizations of any kind in the month prior to the study to avoid lingering immune effects that could be confusing in the safety assessment of the trial.
  • Current use of medication (e.g., levothyroxine, vitamin A supplementation, oral contraceptive use, tetracycline, Diamox etc) that could potentially lead to changes in intracranial pressure
  • Known sensitivity or adverse reaction to anesthetic medications likely to be used in the peri-operative period per the anesthesiologist s evaluation
  • GAN subjects without quantifiable weakness or functional loss
  • Evidence of cardiomyopathy on history, exam, or additional testing (echocardiogram or electrocardiogram) or other cardiac disease that in the opinion of the investigator would deem the subject unsafe to participate in the trial
  • History of diabetes or clinically significant abnormality of glucose tolerance test, fasting blood sugar
  • Positive purified protein derivative testing for tuberculosis
  • Abnormal laboratory values considered clinically significant per the investigator:

    • Platelet count < 100,000 / mm3
    • Persistent leukopenia or leukocytosis (Total white blood cell count < 3,000/mm and > 12,000/mm respectively)
    • Significant anemia [Hb <10 g/dL]
    • Abnormal prothrombin (PT) or partial thromboplastin time (PTT) [value]
    • Abnormal liver function tests (>1.5 X ULN or > 2 X the baseline value)
    • Abnormal pancreatic enzymes (>1.5 X ULN or > 2 X the baseline value)
    • Patients with renal impairment defined as urinary protein concentration >= 0.2 g/L on 2 consecutive tests
  • Failure to thrive, defined as:
  • Falling 20 percentiles (20/100) in body weight in the 3 months preceding Screening/Baseline
  • In patients below the 3rd percentile, any further drop in body weight percentile in the 3 months preceding Screening/Baseline
  • Weight less than < 3rd percentile predicted for age and gender based upon WHO criteria
  • Any anticipated need for major surgery in the next 12 - 18 months (including scoliosis correction surgery)
  • Ongoing medical condition that is deemed by the Principal Investigator to interfere with the conduct or assessments of the study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02362438


Contacts
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Contact: Christopher J Mendoza (301) 402-9080 christopher.mendoza2@nih.gov
Contact: Carsten G Bonnemann, M.D. (301) 594-5496 bonnemanncg@mail.nih.gov

Locations
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United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike Recruiting
Bethesda, Maryland, United States, 20892
Contact: For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR)    800-411-1222 ext TTY8664111010    prpl@cc.nih.gov   
Sponsors and Collaborators
National Institute of Neurological Disorders and Stroke (NINDS)
Investigators
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Principal Investigator: Carsten G Bonnemann, M.D. National Institute of Neurological Disorders and Stroke (NINDS)
Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: National Institute of Neurological Disorders and Stroke (NINDS)
ClinicalTrials.gov Identifier: NCT02362438    
Other Study ID Numbers: 150073
15-N-0073
First Posted: February 13, 2015    Key Record Dates
Last Update Posted: May 27, 2022
Last Verified: January 31, 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: .All subject level data collected as part of the clinical trial will be shared. A CTA has been executed.
Supporting Materials: Study Protocol
Time Frame: At a minimum, the study protocol will be shared with a commercial partner to assist with the BLA. The current CTA requires sharing of data by the end of July 2021; however, there are plans to extend the agreement until July 2023.
Access Criteria: A relationship has been established with a Taysha Gene Therapies. A data analysis plan has not yet been established by the company because NINDS is the current Sponsor.@@@@@@Safety is the primary outcome measure for this clinical trial.

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by National Institutes of Health Clinical Center (CC) ( National Institute of Neurological Disorders and Stroke (NINDS) ):
Intrathecal
AAV9 Mediated Gene Transfer
Phase I
Safety Study
Giant Axonal Neuropathy
Additional relevant MeSH terms:
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Peripheral Nervous System Diseases
Giant Axonal Neuropathy
Neuromuscular Diseases
Nervous System Diseases
Hereditary Sensory and Motor Neuropathy
Nervous System Malformations
Heredodegenerative Disorders, Nervous System
Neurodegenerative Diseases
Polyneuropathies
Congenital Abnormalities
Genetic Diseases, Inborn