A Natural History Study of Biomarkers and Clinical Outcomes in Mucopolysaccharidosis Type IIIA (MPS IIIA; Sanfilippo Syndrome)

Completed

Conditions studied: Mucopolysaccharidosis III-A

In brief

This protocol is a decentralized, single cohort, natural history and biomarker study enrolling up to 20 participants with MPS IIIA (Sanfilippo syndrome). At least 10 participants (\~50%) must be less than four years old at the time of the Parent/LAR consent. The study will have a screening process and 7 study visits, e.g. home visits, that will consist of serum collection and completion of a remote assessment of the Vineland Adaptive Behavior Scales 3rd Edition (Vineland-3) MPS IIIA remains a devastating disease with a high unmet medical need. There is currently a limited number of available data to adequately characterize the progression of the disease. Analysis of blood biospecimens and adaptive behavior in this study will help researchers better understand the clinical progression of MPS IIIA. A better understanding of disease progression may assist in developing novel therapies for rare genetic disorders.

Key facts

Study ID: NCT05523206
Run by: Sanguine Biosciences
People needed: 15
Starts: 2022-09-27
Expected to finish: 2025-01-28
Last updated by the study team: 2025-01-30

Who can join

Age: 0 and older, up to 13. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Age of enrollment is as follows:
All participants must be between 4 months and < 14 years at time of consent
At least 10 participants (ie, approx. 50% of expected total population) must be between 4 months old and < 4 years old at the time of consent
The participant has a confirmed diagnosis of Mucopolysaccharidosis Type IIIA (MPS IIIA) (i.e., Sanfilippo syndrome) based on at least 2 out of the 3 following criteria:
Documented reduced N-sulphoglucosamine sulphohydrolase (SGSH) activity in plasma, white blood cells, and/or skin fibroblasts consistent with MPS IIIA (10% or less of the lower limit of the normal range based on the testing laboratory)
Documented likely pathogenic variant of the SGSH gene
Documented elevated heparan sulfate levels in urine and/or blood Participants and their families are willing to complete 7 blood draws and 7 Vineland-3 collections

You may not qualify if…

Known history of HIV, hepatitis, or other infectious diseases
Taken an investigational product in the last 30 days
Experienced excess blood loss, including blood donation, defined as 80 mL in the last month or 160 mL in the previous two months
Undergone an MPS IIIA gene therapy at any time unless prior Sponsor or designee's approval has been received
Documented loss of activity of sulfatases other than N-sulphoglucosamine sulphohydrolase (SGSH), indicating multiple sulfatase deficiency
Known genetic or acquired disorder associated with developmental delay, seizures or other significant CNS dysfunction that would be expected to confound the clinical or biomarker assessments

Where it is running

Sanguine Biosciences, Inc. — Woburn, Massachusetts, United States

Full record on ClinicalTrials.gov

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