Liabilities / Assets
67th percentile
Tied with the lowest-debt nonprofits in its peer group.
The Champ Foundation
990EZ • Fiscal year 2016 • EIN 47-5555752
Siviq Scores
Precomputed percentiles for this filing year versus similar nonprofits in the same peer cohort.
0.00x
Liabilities / Revenue
65th percentile
Tied with the lowest-debt nonprofits in its peer group.
Net Margin
93rd percentile
Higher net margin than 93% of similar nonprofits.
Top Officer Pay
87th percentile
Higher top officer pay than 87% of similar nonprofits.
Top officer pay equals 0.0% of source-year revenue.
Asset Growth
89th percentile
Faster asset growth than 89% of similar nonprofits.
Revenue Growth
85th percentile
Faster revenue growth than 85% of similar nonprofits.
Balance Sheet
Assets
Up$239,382
Up $132,499 (+124%) from 2015
Net Assets
$239,382
No earlier filing loaded for comparison.
Liabilities
Flat$0
Flat from 2015
Revenue And Expenses
Revenue
Up$183,623
Up $76,037 (+71%) from 2015
Expenses
Up$51,124
Up $50,421 (+7172%) from 2015
Net Income
Up$132,499
Up $25,616 (+24%) from 2015
Historical Trend
Jump To
Filing Snapshot
- Filing Period
- Jan 1, 2016 to Dec 31, 2016
- Signed
- May 12, 2017
- Return Version
- 2016v3.0
- Gross Receipts
- $189,620
Mission and Program Overview
Mission
The Champ Foundation supports research toward better treatment and a cure for diseases caused by mitochondrial DNA deletions, with an emphasis on Pearson Syndrome. These diseases are very rare; for example, there have only been around 100 cases of Pearson Syndrome described in the literature since its discovery in 1979. Current "treatments" only address symptoms as they present themselves. Therefore, The Champ Foundation seeks to fund research that speeds the development of treatment and a cure.
Program Services
| Description | Grants | Expenses |
|---|---|---|
| In 2016, The Champ Foundation began to fund research toward better treatment and a cure of Pearson Syndrome and mitochondrial DNA deletion disorders by making its first grant to Dr. Suneet Agarwal at Boston Children's Hospital. "Mitochondrial genome editing for Pearson marrow pancreas syndrome," at Boston Children's Hospital, aims to establish the efficacy of genetic editing tools to shift heteroplasmy (the balance of defective vs. healthy mitochondria). The Champ Foundation made a $100,000 commitment to this project with the stipulation that no portion be used for indirect costs. The funding restarted the laboratory's efforts to understand and treat Pearson Syndrome. These efforts had been abandoned, after significant progress, due to lack of funding. A post-doctoral researcher is dedicated to the project full-time. The project characterizes The Champ Foundation's approach. We seek out talented researchers at excellent institutions, whose intellectual interest in mitochondrial DNA deletion disorders has been hindered by financial concerns. We believe that these diseases can be treated and cured, provided that capable researchers and clinicians are aware of the problem and allowed to pursue a solution. | $50,000 | $0 |
| Also in 2016, The Champ Foundation established procedures to call for grants and a peer-review process for those grants prior to funding. This process was constructed an implemented by The Champ Foundation's vice-president, at no cost to the foundation. As a result of the first call for grants, The Champ Foundation's volunteer scientific advisory board reviewed five grants from across the globe. Two of these grants will receive funding in 2017! | $0 | $0 |
Compensation and Service Providers
Employees
| Name | Title | Full / Part Time | Base | Other | Total |
|---|---|---|---|---|---|
| Jeffrey Reynolds | President | PT | $0 | - | - |
| Elizabeth Reynolds | Vice President | PT | $0 | - | - |
| Elizabeth Malkin | Secretary | - | $0 | - | - |
| Tyler Albright | Treasurer | - | $0 | - | - |
| Walker Cole Arledge | Director | - | $0 | - | - |
Fundraising, Events, and Gaming
Fundraising Events
| Event | Gross Receipts | Gross Revenue | Direct Expenses | Net Income |
|---|---|---|---|---|
| Buffalo Event | $79,406 | $15,504 | $0 | $15,504 |
| Total Events | $79,406 | $15,504 | $5,997 | $9,507 |
Filing and Contact Details
Filer
- Filer Name
- Champ Foundation
- EIN
- 47-5555752
- Phone
- 7278712667
- Address
- 2712 LITTLE ROGERS ROAD, DURHAM, NC 27704
Signing Officer
- Name
- Jeffrey Reynolds
- Title
- President
- Phone
- 7278712667
- Signed
- 2017-05-12
Supplemental Narrative
Additional Explanations
Form 990-EZ, Part I, Line 10
“Grant to Boston Children's Hospital to support Dr. Suneet Agarwal's project "Mitochondrial genome editing for Pearson marrow pancreas syndrome."”
Form 990-EZ, Part I, Line 16
“PayPal, CrowdRise and PNC Bank Fees.”
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| IRS990EZ/PrimaryExemptPurposeTxt | 0 | The Champ Foundation supports research toward better treatment and a cure for diseases caused by mitochondrial DNA deletions, with an emphasis on Pearson Syndrome. These diseases are very rare; for example, there have only been around 100 cases of Pearson Syndrome described in the literature since its discovery in 1979. Current "treatments" only address symptoms as they present themselves. Therefore, The Champ Foundation seeks to fund research that speeds the development of treatment and a cure. |
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| IRS990EZ/ProgramSrvcAccomplishmentGrp/DescriptionProgramSrvcAccomTxt | 0 | In 2016, The Champ Foundation began to fund research toward better treatment and a cure of Pearson Syndrome and mitochondrial DNA deletion disorders by making its first grant to Dr. Suneet Agarwal at Boston Children's Hospital. "Mitochondrial genome editing for Pearson marrow pancreas syndrome," at Boston Children's Hospital, aims to establish the efficacy of genetic editing tools to shift heteroplasmy (the balance of defective vs. healthy mitochondria). The Champ Foundation made a $100,000 commitment to this project with the stipulation that no portion be used for indirect costs. The funding restarted the laboratory's efforts to understand and treat Pearson Syndrome. These efforts had been abandoned, after significant progress, due to lack of funding. A post-doctoral researcher is dedicated to the project full-time. The project characterizes The Champ Foundation's approach. We seek out talented researchers at excellent institutions, whose intellectual interest in mitochondrial DNA deletion disorders has been hindered by financial concerns. We believe that these diseases can be treated and cured, provided that capable researchers and clinicians are aware of the problem and allowed to pursue a solution. |
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| ReturnHeader/BuildTS | 0 | 2017-02-10 21:41:12Z |
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Document Assets
No mirrored PDF or thumbnail assets are attached yet.
Filings
Displayed year
2016 • Form 990EZDetailed filing. Detailed filing data is available for this year.
- Assets
- $239,382
- Liabilities
- $0
- Net assets
- $239,382
- Revenue
- $183,623
- Expenses
- $51,124
- Net income
- $132,499