Cure SPG4 Foundation is a nonprofit organization founded in 2020, committed to increasing awareness and providing resources for families affected by SPG4 Hereditary Spastic Paraplegia, a rare neurological condition affecting mobility. They aim to fund research leading to a potential cure for this devastating condition.
2020
85-4389675
$132.3 thousand
This organization contributes to the following United Nations Sustainable Development Goals. See the SDG page for more information.
SPG4 is the most common subtype of Hereditary Spastic Paraplegia, characterized by muscle weakness and difficulty walking.
Founded by families affected by SPG4, our journey sheds light on the challenges faced.
Participating in innovative gene therapy research aimed at treating SPG4.
Research focused on using AAV9 gene therapy to correct the gene mutation causing SPG4.
Learn MoreStudies to understand the progression of SPG4 through participant data.
Overall Score
46
34
/100
Program Expense Ratio
100.00%
20
/20
Program Revenue Growth
0.00%
2
/20
Leverage Ratio
0
2
/20
Working Capital Ratio
0.8066
8
/20
Fundraising Efficiency
0
2
/20
Fiscal Year:2023
Source:Source: Self-reported by organization
Category | Amount | Percentage |
---|---|---|
Contributions, Gifts, and Grants | 275.2K | 96.00% |
Program Services | 0 | 0.00% |
Investment Income | 0 | 0.00% |
Sales of Non-Inventory Assets | 0 | 0.00% |
Other Notable Sources | 0 | 0.00% |
Total Revenue | 286.6K | 100.00% |
Health Associations
Genetic DisordersHealth Associations
Genetic DisordersHealth Associations
Genetic DisordersHealth Associations
Genetic DisordersHealth Associations
Genetic Disorders