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A Study to Prospectively Assess Disease Progression in Male Children With X-ALD

N

NeuroVia

Status

Unknown

Conditions

X-Linked Adrenoleukodystrophy

Study type

Observational

Funder types

Industry

Identifiers

NCT03278899
NV1205-008

Details and patient eligibility

About

This is a non-interventional, multi-center study that follows general principles of periodic assessment of X-ALD patients in routine practice. No study drug treatment will be given and no changes to patient treatment are necessary.

Full description

This is a non-interventional, multi-center study that follows general principles of periodic assessment of X-ALD patients in routine practice. No study drug treatment will be given and no changes to the patient treatment are necessary.

Patients with X-ALD will be recruited and invited to attend a baseline visit. After eligible patients are enrolled, retrospective and baseline data will be collected. After enrollment, patients will be seen approximately every 6 months until they meet withdrawal criteria or the Sponsor terminates the study.

Enrollment

100 estimated patients

Sex

Male

Ages

2 to 13 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed informed consent by patient's parent(s)/legally acceptable representative(s). In addition, signed children's assent form according to local requirements.

  • Males patients 2-13 years of age with a confirmed diagnosis of X-ALD that fall into one of the following:

    • Asymptomatic patients without MRI evidence of cerebral involvement
    • Patients with MRI evidence of cerebral involvement (Loes score ≥0.5) with or without clinical symptoms
    • Patient who have HSCT within 3 months from enrollment

Exclusion criteria

  • Patients who are 14 years of age or older
  • Patients who are in a vegetative state
  • Patients (or their guardians) who are unwilling or unable to comply with the study procedures
  • Patients who received HSCT more than 3 months before enrollment

Trial contacts and locations

3

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Central trial contact

Program Director

Data sourced from clinicaltrials.gov

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