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Natural History Study of Patients With Canavan Disease (CANinform Study)

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Aspa Therapeutics

Status

Active, not recruiting

Conditions

Canavan Disease

Study type

Observational

Funder types

Industry

Identifiers

NCT04126005
CANinform (Other Identifier)
CVN-101

Details and patient eligibility

About

This study uses medical records that allow retrospective data extraction of critical milestone and motor function data. In addition, prospective assessments collect data relevant to the natural history of Canavan disease in children.

Full description

The CANinform natural history study is the first multinational effort to rigorously gather both retrospective and prospective data from this patient population. Data collection includes extraction of retrospective data from medical records of living and deceased patients, and collection of prospective, longitudinal data from living patients and their parent(s)/caregiver(s). Motor function assessments are performed remotely in the home via video or in the clinic by qualified study team members. Families will be invited to attend clinic visits and/or will be followed remotely by the clinical site for approximately 3 years.

Enrollment

70 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Meet age criteria of a specific cohort.
  2. Confirmed clinical and biochemical diagnosis of Canavan disease.
  3. Available medical records since birth that permit documentation of disease characteristics and developmental milestones.
  4. Parent and/or legal guardian is able to read, understand, and sign the informed consent.

Exclusion criteria

  1. Patient does not meet the Inclusion Criteria.

Trial design

70 participants in 5 patient groups

Cohort 1 (Age < 18 Months)
Description:
* Motor function assessments (remote or in-clinic) every 2 months * Clinic assessments every 6 months
Cohort 2 (Age ≥ 18 Months - 3 Years)
Description:
* Motor function assessments (remote or in-clinic) every 4 months * Clinic assessments every 6 months
Cohort 3 (Age > 3 - 5 Years)
Description:
* Motor function assessments (remote or in-clinic) every 6 months * Clinic assessments every 6 months
Cohort 4 (Age > 5 Years)
Description:
* Motor function assessments (remote or in-clinic) 12 months * Clinic assessments every 12 months
Cohort 5 (Deceased)
Description:
• The patient's medical history records will be reviewed. In addition, a parent interview will be performed.

Trial contacts and locations

3

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Central trial contact

clinicaltrials@aspatx.com; Mary Rohrer, RN, BSN

Data sourced from clinicaltrials.gov

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