Prospective Longitudinal Study of Neurological Disease Trajectory in Children Living With Late-Infantile or Juvenile Onset of GM1 or GM2 Gangliosidosis
| Registry | NCT05109793, acronym PRONTO |
|---|---|
| Status | Completed |
| Study type | Observational |
| Enrollment | 31 (Actual) |
| Sponsor | Azafaros B.V. (Industry) |
| Conditions | GM1 Gangliosidosis, Sandhoff Disease, Tay-Sachs Disease |
| Dates | start 2022-02-22, primary completion 2025-09-16, completion 2025-09-16, first posted 2021-11-05, last updated 2025-09-29 |
| Locations | 13 sites in United States, Brazil, France, Germany, Italy, United Kingdom |
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The study aims to characterize prospectively longitudinal progression of neurological domains in GM1 and GM2 Gangliosidosis patients with high-quality standards (GCP compliant).
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.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Cohort | Late infantile or juvenile onset for GM1 or GM2 Gangliosidosis. The study anticipates to include a total of approximately 35 patients. |
Sex: All, ages: 2 Years to 20 Years
Inclusion Criteria: * 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 Exclusion Criteria: * 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
| Facility | City | Country | Status |
|---|---|---|---|
| UCSF Benioff Children's Hospital | Oakland, California | United States | |
| Mayo Clinic Rochester | Rochester, Minnesota | United States | |
| Hospital Pequeno Principe | Curitiba | Brazil | |
| Hospital de Clinicas de Porto Alegre | Porto Alegre | Brazil | |
| Hopital d'Enfants CHU Timone | Marseille | France | |
| Armand-Trousseau Children's Hospital - CHU Paris Est | Paris | France | |
| Hôpital des Enfants - CHU Toulouse Purpan | Toulouse | France | |
| Universtitäsklinikum Giessen und Marburg | Giessen | Germany | |
| LMU - Klinikum der Universitaet Muenchen - Neurologische Klinik und Poliklinik | Munich | Germany | |
| Universita' di Catania | Catania | Italy | |
| Fondazione IRCCS Istituto Neurologico Carlo Besta | Milan | Italy | |
| University Hospital Friuli Centrale | Udine | Italy | |
| Great Ormond Street Hospital NHSFT | London | United Kingdom |