This study is in progress, not accepting new patients

GM1 and GM2 Gangliosidosis PROspective Neurological Disease TrajectOry Study (PRONTO)

a study on GM1 Gangliosidosis Sandhoff Disease Tay-Sachs Disease

Summary

Eligibility
for people ages 2-20 (full criteria)
Location
at UCSF
Dates
study started
completion around

Description

Summary

The study aims to characterize prospectively longitudinal progression of neurological domains in GM1 and GM2 Gangliosidosis patients with high-quality standards (GCP compliant).

Official Title

Prospective Longitudinal Study of Neurological Disease Trajectory in Children Living With Late-Infantile or Juvenile Onset of GM1 or GM2 Gangliosidosis

Details

The study is a prospective longitudinal, multicentric decentralized trial which will be performed in children diagnosed with late infantile or juvenile onset of neurological disease of either GM1 or GM2 Gangliosidoses (Tay-Sachs or Sandhoff disease). The study anticipates to include a total of approximately 35 patients. A large set of neurological functions will be evaluated by rating scales used by physicians and questionnaires answered by parents. Digital tools will be used to support the study procedures with virtual visits and also a passive monitoring approach with a medical device.

Keywords

GM1 Gangliosidosis, Sandhoff Disease, Tay-Sachs Disease, GM2 Gangliosidosis, Natural History Study, Lysosomal Storage Disorders, Nervous System Diseases, Genetic Diseases, Inborn, Hexosaminidase A and B deficiency, β-galactosidase deficiency, Gangliosidoses, GM2 Gangliosidoses

Eligibility

You can join if…

Open to people ages 2-20

  • Genetically confirmed GM1 Gangliosidosis or genetically confirmed Tay-Sachs or Sandhoff disease
  • Onset of neurological symptoms on or after the patient's first birthday
  • Achieved 12-month developmental milestones at normal developmental time points as per Principal Investigator's judgement
  • Abnormal gait and/or speech disturbance

You CAN'T join if...

  • Patients who have received (within 6 months before screening), are currently receiving or are planned to receive (within the following 6 months) gene therapy, stem cell transplantation, experimental drugs, or any drug, which, in the Investigator´s opinion, may (have) interfere(d) with disease progression

Locations

  • UCSF Benioff Children's Hospital
    Oakland California 94609 United States
  • Mayo Clinic Rochester
    Rochester Minnesota 55905 United States

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Azafaros A.G.
ID
NCT05109793
Study Type
Observational
Participants
About 31 people participating
Last Updated