Natural History Study in Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia

Overview

Información sobre este estudio

The purpose of this study is to collect data to contribute to the development of future novel therapies, including VGL101, that focus on the neuropathophysiological features that underlie adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and that are essential to reverse, delay, or stop progression of this debilitating disorder.

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a rare, rapidly progressing, genetic, neurodegenerative disease for which no definitive treatment options and limited information on the natural history of the disease are available. The structural, genetic, and neuropathophysiological abnormalities of ALSP lead to the onset of neurologic symptoms, such as moderate to severe motor and neuropsychiatric impairments. 

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Key Inclusion Criteria for both Definitive ALSP patients and Prodromal ALSP patients:

1. Subjects who have documentation of a gene mutation in the CSF1R gene

Key Inclusion Criteria for Definitive ALSP patients, only:

1. Subjects who fulfill both of the following criteria (a and b):

a. More than two findings of clinical signs or symptoms in the following categories:
i. Cognitive impairment or psychiatric problem ii. Pyramidal signs on neurological
examination iii. Extrapyramidal signs, such as rigidity, tremor, abnormal gait, or
bradykinesia iv. Epilepsy b. MRI findings consistent with ALSP: specifically,
bilateral cerebral white matter lesions with or without thinning of the corpus
callosum NOTE: Subjects with other causes of leukoencephalopathy, including vascular
dementia, multiple sclerosis, or leukodystrophy (e.g., adrenoleukodystrophy, Krabbe
disease, metachromatic leukodystrophy), will be excluded.

2. Subjects who, in the investigator's opinion, have demonstrated clinical progression of
their ALSP within the past year.

3. Subjects who meet the criteria for definitive ALSP must have a designated caregiver
who spends at least 4 hours per week with them. The caregiver must be able and willing
to assist the subject in complying with the study requirements, be able to provide
information during study visits, and be willing to sign a caregiver ICF.

Key Inclusion Criteria for Prodromal ALSP patients, only:

1. MRI findings consistent with ALSP: specifically, bilateral cerebral white matter lesions
with or without thinning of the corpus callosum. Prodromal subjects may have none or up to
and including 2 ALSP-related clinical signs or symptoms (i.e., they do not meet the
clinical criteria outlined in the Definitive ALSP as "more than two").

Key Exclusion Criteria (for all study participants):

1. Subjects with any neurological or psychiatric diseases that can produce cognitive,
motor, or behavioral impairment similar to ALSP, including, but not limited to,
Alzheimer's disease, frontotemporal dementia, ALS, stroke, Huntington disease,
multiple sclerosis, Parkinson's disease, and Down syndrome, or with active
alcohol/drug abuse

2. Subjects who are unable to undergo MRI

3. Subjects with any condition or situation that, in the opinion of the investigator or
sponsor medical personnel, may place the subject at significant risk, confound the
study results, or interfere significantly with the subject's participation in the
study.

4. Subjects who have previously undergone HSCT or plan to undergo HSCT within 12 months
of the Screening/Baseline visit.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 1/30/2024. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Zbigniew Wszolek, M.D.

Abierto para la inscripción

Contact information:

Audrey Strongosky C.C.R.C.

Strongosky.Audrey2@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20522392

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