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NCT Number: NCT07215416

Safety and Efficacy of Mutation-targeted Precision Genetic Therapy for Ataxia-Telangiectasia (A-T)

This project aims to evaluate the safety and efficacy of precision genetic therapy for patients with Ataxia-telangiectasia (A-T), a rare neurodegenerative disease caused by mutations in the ATM gene. The investigators will conduct a clinical trial to study the safety and efficacy of intrathecal administration of atipeksen, a targeted genetic therapy that restores ATM gene function in A-T individuals bearing the recurrent ATM c.7865C>T variant. The aim of this study is to delay or forestall progression of neurologic symptoms in A-T and improving quality of life. Success will provide an empirical foundation for advancing additional precision genetic therapies for A-T and other neurodegenerative conditions.

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Key information

About this study

The goal of this protocol is to study the safety and efficacy of the investigational drug atipeksen, a mutation-specific antisense oligonucleotide (ASO), in individuals with ataxia telangiectasia (A-T). The first objective is to evaluate the safety of therapy with atipeksen, a 22-nucleotide oligonucleotide designed to ameliorate the effects of mis-splicing caused by a mutation in the ATM gene(NM_000051.3), c.7865C>T (p.Ala2622Val), when administered via intrathecal injection. The second objective is to determine if administration of intrathecal atipeksen can reduce or stabilize neurological decline using clinical and physiological biomarkers. The primary endpoint will be serial clinical neurologic assessments using the Ataxia-Telangiectasia Neurological Examination Toolkit (A-T NEST) and a structured version of the Ataxia-Telangiectasia Clinical Global Impression of Change (A-T CGI). Secondary endpoints will include videotaped clinical neurological examinations, movement pattern analyses using wearable actigraphy, and standard scales administered by PT, OT, and neuropsychology. Exploratory endpoints include serial brain imaging with volumetric analyses, neurofilament light chain, alpha-fetoprotein, and growth parameters.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

INCLUSION/EXCLUSION CRITERIA:

Who can take part:

  • People with classic A-T confirmed by genetic testing
  • Must have a specific ATM gene change (c.7865C>T)
  • Must also have another ATM change that causes A-T

Who cannot take part:

People with health problems that make lumbar puncture unsafe:

  • Blood clotting or bleeding problems
  • Brain conditions raising pressure inside the head
  • Serious heart or breathing problems
  • Infection near the lower back

Other things doctors will check:

  • Overall health and stability
  • Any medicines that might cause problems
  • Past difficulties with lumbar punctures
  • Any other safety concerns

Treatment and study plan

Antisense oligonucleotide targeting the ATM gene

Drug

Atipeksen is a fully modified PS-2'MOE splice-switching antisense oligonucleotide that is designed to restore normal splicing patterns in patients with the ATM c.7865C>T mutation.

Primary outcomes

  1. Neurological function as measured by the AT-NEST scale

    Time frame: At Baseline and every 12 weeks up to ten years

    The Ataxia-Telangiectasia Neurological Examination Toolkit (AT-NEST) is a test designed specifically for people with Ataxia-Telangiectasia (A-T). It helps doctors and researchers understand how the brain and nerves are working. The test looks at six main areas:

    • Communication
    • Eye movements Ataxia (problems with balance and coordination)
    • Movement disorders
    • Muscle strength (Power)
    • Nerve function (Neuropathy) These six areas make up the "pure neuro" score, which ranges from 0 (lowest) to 100 (highest). The test also includes growth and nutrition. When these are added to the six main areas, a total "neuro-related" score is calculated, with a maximum of 114. Higher scores mean better overall performance.This test is not painful and is carried out by trained specialists who will guide you through each step.
  2. Ataxia-Telangiectasia Structured Clinical Global Impression of Change (A-T CGI)

    Time frame: At Baseline and every 12 weeks up to ten years

    The Ataxia-Telangiectasia Clinical Global Impression of Change (AT-CGI) is a tool used to track how A-T progresses over time. It looks at five main areas of the disease:

    Ataxia (balance and coordination problems) Dysarthria (difficulty speaking) Repetitive movements / Dysmetria (trouble controlling movements) Movement disorders Eye movements

    Each area is scored from 0 to 4, for a total of 20 points. Higher scores mean more severe symptoms, while lower scores indicate better function.

Secondary outcomes

  1. Motor performance as measured by the Bruininks-Oseretsky Test of Motor Proficiency 2nd edition

    Time frame: Baseline and every 6 months up to 10 years

    The Bruininks-Oseretsky Test of Motor Proficiency 2nd edition (BOT-2) is a simple way for therapists to check how your child is developing movement skills. It looks at:

    • Small hand and finger movements (fine motor)
    • How quickly and accurately hands are used (dexterity)
    • Big movements like running or jumping (gross motor)
    • How well the body works together (coordination) During the test, the child does different activities, and each one is scored. These scores are added up to give both an overall score (out of 200 points) and separate scores for each skill area. The results are then compared to what is typical for children of the same age.
  2. Performance and goal satisfaction as measured by the Canadian Occupational Performance Measure (COPM)

    Time frame: Baseline and every 6 months up to 10 years

    The Canadian Occupational Performance Measure (COPM) is a test done by an occupational therapist to understand what daily activities are most important to a person and how well they feel they can do them. During the test, the person picks up to five activities they find difficult or want to improve. For each activity, they rate:

    • How well they can do it
    • How satisfied they are with their performance Both scores range from 1 to 10 (higher numbers mean better performance or more satisfaction). The scores are then averaged to see overall progress. The main goal is to track improvements over time, especially before and after a therapy or intervention.
  3. Performance in activities of daily living as measured by the Pediatric Evaluation of Disability Inventory Computer Adaptive Test

    Time frame: Baseline and every 6 months up to 10 years

    The Pediatric Evaluation of Disability Inventory - Computer Adaptive Test (PEDI-CAT) is a questionnaire filled out by parents or caregivers. It helps us understand how a child is doing in everyday life. It looks at four areas:

    • Daily activities (like eating, dressing, and personal care)
    • Mobility (how a child moves around)
    • Social/cognitive (how a child plays, communicates, and learns)
    • Responsibility (how much a child can manage tasks at home or in the community) The test is "adaptive," meaning the questions change depending on how you answer, so it fits your child's abilities. Each area gets a score from 0 to 100, with higher scores meaning better functional ability.
  4. Visual-motor function as measured by the Beery-Buktenica Developmental Test of Visual Motor Integration

    Time frame: Baseline and every 6 months up to 10 years

    The Beery-Buktenica Developmental Test of Visual-Motor Integration (Beery-VMI) is a test often given by occupational therapists to see how well a child's eyes and hands work together. During the test, the child copies shapes and designs that get harder as the test goes on. Sometimes the child may also be asked to find differences between pictures or match patterns. The results show:

    • A standard score with a range of 45 to 155; higher scores indicate a better performance
    • A percentile score, which shows what percentage of children the same age scored lower.

    This helps parents and therapists see how the child's coordination and fine motor skills are compared to others their age.

  5. Neurodevelopmental function, as measured by the Leiter International Performance, third edition

    Time frame: Baseline and yearly up to 10 years

    The Leiter International Performance Scale-3 (Leiter-3) is a test that measures thinking and problem-solving skills. It is especially helpful for children or adults who have speech, language, or learning difficulties, or for those who do not speak English. The test looks at areas such as:

    • Problem-solving and reasoning
    • Attention and memory Visual and spatial skills (understanding shapes, patterns, and space) The results include an IQ score (higher scores mean stronger skills). Subtest scores range from 0 to 20 and composite scores range from 30 to 170; higher scores indicate a better outcome.

    This helps show how a person's thinking skills compare to others their age.

  6. Neurodevelopmental function, as measured Wechsler Intelligence Scale for Children, fifth edition

    Time frame: Baseline and yearly up to 10 years

    he Wechsler Intelligence Scale for Children - Fifth Edition (WISC-V) is a test that measures different areas of a child's thinking and learning. It looks at skills such as:

    • Understanding and using language (verbal comprehension)
    • Solving puzzles and understanding visual information (visual-spatial)
    • Problem-solving and reasoning (fluid reasoning)
    • Remembering information (working memory)
    • How quickly the brain processes information (processing speed) Subtests have scaled scores with a range of 1 to 19 and composites have standard scores with a range from 45 to 155; higher scores indicate a better outcome.

    The test gives a Full Scale IQ (FSIQ) score, which shows a child's overall level of thinking skills. Higher scores mean stronger abilities.

  7. Neurodevelopmental function, as measured by the Vineland Adaptive Behavior Scale

    Time frame: Baseline and yearly up to 10 years

    The Vineland Adaptive Behavior Scales, Third Edition (Vineland-3) is a test that measures how a child or adult manages everyday life skills, also called adaptive behaviors.It looks at areas such as:

    • Communication (understanding and using language)
    • Daily living skills (self-care, getting dressed, eating)
    • Socialization (interacting with others)
    • Motor skills (movement and coordination) Subtests are calculated as v-Scale scores with a possible range of 1 to 19. Composite scores are Standard Scores with a range of 20 to 140. Higher scores indicate a better outcome Growth scale values (GSVs) describe the participant's absolute level of performance on a test. Range is 10 to 220. Higher scores indicate better performance The results are turned into scores that show how well a person is functioning in daily life. Higher scores mean stronger everyday skills.
  8. Motor performance through digital wearable actigraphs

    Time frame: Baseline and every 12 weeks up to 10 years

    Digital actigraphs are small motion sensors that track how a person moves during daily life. They are often used in people with movement disorders, like ataxia and ataxia-telangiectasia.

    In this study, participants will wear one sensor on the wrist and one on the ankle for one week at a time. The information collected will show how a person moves during everyday activities. These results will then be compared to others with ataxia-telangiectasia who are not receiving treatment.

Study contacts

Contact information is provided by the study sponsor or research team.

Arya Newington

CONTACT

[email protected]

617-919-7499

Sponsors and collaborators

Lead sponsor

Timothy Yu

Other

Registry information

Official study title

A Phase 1/2 Study of Antisense Oligonucleotide Therapy for Treatment of Ataxia-Telangiectasia

Important dates

Study start
2026
Primary completion
2032
Study completion
2036
First posted
Oct 10, 2025
Registry last updated
May 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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