The National PKU Alliance (NPKUA) is dedicated to enhancing the lives of individuals and families affected by Phenylketonuria (PKU), a rare metabolic disorder. Founded in 2008, NPKUA aims to be the principal resource for anyone impacted by PKU through education, support, and research advocacy. The organization conducts various initiatives including community-building events, facilitation of clinical research, and legislative advocacy to ensure access to necessary treatment and support for PKU individuals across their life stages.
2008
26-2849140
$4.757 million
This organization contributes to the following United Nations Sustainable Development Goals. See the SDG page for more information.
Join regional fundraising events aimed at supporting PKU research.
Engaging the community to lobby for essential medical coverage.
Attend the largest gathering for the PKU community to share and learn.
Lifting the Limits Fundraising
Organized over 10 Lifting the Limits events raising significant funds for PKU research.
Patient Registry Launch
Launched the PKU Patient Registry to accelerate research and gather community data.
Research Grants
Provided over $5 million in research grants to advance PKU studies.
Overall Score
64
50
/100
Program Expense Ratio
54.80%
4
/20
Program Revenue Growth
-69.99%
2
/20
Leverage Ratio
0.03369
20
/20
Working Capital Ratio
2.452
16
/20
Fundraising Efficiency
2.37
8
/20
Fiscal Year:2023
Source:Source: Self-reported by organization
Category | Amount | Percentage |
---|---|---|
Contributions, Gifts, and Grants | 1.513M | 115.89% |
Program Services | 13.5K | 1.03% |
Investment Income | 103.9K | 7.95% |
Sales of Non-Inventory Assets | 39.6K | 3.03% |
Other Notable Sources | 5K | 0.38% |
Total Revenue | 1.306M | 100.00% |
Med Research
Down Syndrome ResearchMed Research
Down Syndrome ResearchMed Research
Down Syndrome ResearchMed Research
Down Syndrome ResearchMed Research
Down Syndrome Research