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| Name | Class |
|---|---|
| Silverstein Foundation | UNKNOWN |
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The New York Stem Cell Foundation (NYSCF) Research Institute is performing this research to accelerate Parkinson's disease research and drug development by using cells from the body (such as skin or blood cells) to make stem cells and other types of cells, conduct research on the samples, perform genetic testing, and/or store the samples for future use.
Through this research, researchers hope to identify future treatments or even cures for Parkinson's disease.
Researchers at the New York Stem Cell Foundation (NYSCF) Research Institute study diverse diseases, conditions, and traits by creating stem cells from biological samples. These "pluripotent" stem cells can become any cell in the human body, including cells that may be difficult, invasive, or impossible to obtain directly.
Additionally, researchers perform genetic testing to learn more about DNA, a material in most cells that contains instructions for the body's development and functions (such as traits like eye color and risk of certain diseases). A piece of DNA that determines the specific role of a cell is called a "gene." If the instructions in a gene are abnormal, this can lead to disease.
Participation in the study involves: (1) completion of health questionnaires, (2) providing a skin and/or blood sample from which stem cells may be created, (3) collection of a saliva sample for genetic analysis, and (4) possible future follow-up to provide additional information or learn about other research studies.
This study is not a clinical trial.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Parkinson's Disease | Subjects in this group will have a diagnosis of Parkinson's disease with or without a known GBA gene mutation. |
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| Gaucher Disease | Subjects in this group with have a diagnosis of Gaucher disease with or without a known GBA gene mutation. |
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| Healthy Control | Subjects in this group will serve as healthy controls. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Biological Sample Collection | Other | Skin biopsy (2-3mm) and/or blood (up to 50 mL); saliva; excess/leftover biospecimens that were (or will be) collected for other purposes (e.g., medical procedure) |
| Measure | Description | Time Frame |
|---|---|---|
| Establishment of a diverse bank of biological samples, stem cell lines, derivatives, and associated information. | Establish a robust disease signature using a cohort of PD and carefully matched control samples to screen a library of approximately 3,000 compounds to determine whether any compounds improve or reverse disease phenotypes. | Baseline |
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Inclusion Criteria:
Exclusion Criteria:
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Individuals with a diagnosis of one or more of the listed conditions.
Individuals without a condition to serve as healthy controls (a comparison group for those with conditions).
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Clinical Research Office | Contact | 212-927-1801 | clinicalresearch@nyscf.org |
| Name | Affiliation | Role |
|---|---|---|
| Laura Andres-Martin | New York Stem Cell Foundation Research Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The New York Stem Cell Foundation Research Institute | Recruiting | New York | New York | 10019 | United States |
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| ID | Term |
|---|---|
| D010300 | Parkinson Disease |
| D005776 | Gaucher Disease |
| ID | Term |
|---|---|
| D020734 | Parkinsonian Disorders |
| D001480 | Basal Ganglia Diseases |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
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Skin biopsy (2-3mm) and/or blood (up to 50 mL); saliva; excess/leftover biospecimens that were (or will be) collected for other purposes (e.g., medical procedure)
|
| D009422 | Nervous System Diseases |
| D009069 | Movement Disorders |
| D000080874 | Synucleinopathies |
| D019636 | Neurodegenerative Diseases |
| D013106 | Sphingolipidoses |
| D020140 | Lysosomal Storage Diseases, Nervous System |
| D020739 | Brain Diseases, Metabolic, Inborn |
| D001928 | Brain Diseases, Metabolic |
| D008661 | Metabolism, Inborn Errors |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D008064 | Lipidoses |
| D008052 | Lipid Metabolism, Inborn Errors |
| D016464 | Lysosomal Storage Diseases |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D052439 | Lipid Metabolism Disorders |