Niemann Pick Diseases

3

Review clinical trials related to Niemann Pick Diseases. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Retinal Hyperspectral Imaging in Neurodegenerative Diseases

Hyperspectral retinal imaging is a non-invasive imaging modality in which a series of images of the retina are captured using light of different wavelengths. The resulting "hypercube" of data provides a wealth of information about the retinal structure. Our group has developed evidence supporting a role for this technology in the detection of retinal amyloid beta in Alzheimer's disease. We are undertaking further studies to establish the role of this method in the assessment of people with dementia, or those at risk of Alzheimer's disease. In addition, we wish to test whether the approach may have value in other forms of dementia or neurodegenerative disease such as Parkinson's disease, Lewy-Body dementia or vascular dementia.

Participants needed: 930
Trial details
Age: 30+Biological sex: AllType: InterventionalSponsor: Center for Eye Research AustraliaUpdated: Apr 22, 2026Locations: 1
Eligibility criteria

Aged over 30 years. [+5]

Inability to provide informed consent [+3]

Status: Recruiting

Longitudinal Study of Neurodegenerative Disorders

The purpose of this study is to understand the course of rare genetic disorders that affect the brain. This data is being analyzed to gain a better understanding of the progression of the rare neurodegenerative disorders and the effects of interventions.

Participants needed: 1,500
Trial details
Biological sex: AllType: ObservationalSponsor: University of PittsburghUpdated: Feb 9, 2026Locations: 1
Eligibility criteria

Any patient with a genetic neurodegenerative disorder

none

Status: Recruiting

A Real-world Long-term Safety and Immunogenicity Study of Olipudase Alfa Therapy in Pediatric Patients Less Than 2 Years of Age With Acid Sphingomyelinase Deficiency (ASMD)

US, multicenter, cohort, open label observational study with primary data collection. Ancillary protocol-specified procedures to address the study objectives (eg, assessment of ADA) may be considered outside the standard of care for acid sphingomyelinase deficiency (ASMD), but the study methodology remains non-interventional, as the additional collection of data from participants will not dictate treatment. The total overall study duration will be 5 years. The follow-up period will be a minimum of 1 year to a maximum of 3 years. The enrollment period will be up to 4 years, to allow a minimum of 1 year of follow-up for the last participant enrolled.

Participants needed: 10
Trial details
Age: Up to 2Biological sex: AllType: ObservationalSponsor: SanofiUpdated: Oct 31, 2025Locations: 5
Eligibility criteria

The participant must have ASMD type A/B or B and must be <2 years of age at the... [+4]

The participant has received an investigational drug within 30 days or 5 drug ha... [+2]