Overview
What is The Mpn Research Foundation?
The Mpn Research Foundation, situated in Chicago, Illinois, is a dedicated nonprofit organization that channels its resources into investigating Polycythemia Vera, Primary Myelofibrosis, and Essential Thrombocythemia, commonly referred to as MPNs. Their primary mission is to foster, finance, and support groundbreaking research aimed at uncovering the causes, developing effective treatments, and potentially discovering a cure for these conditions. The foundation actively encourages collaboration within the scientific community to expedite MPN research progress. With a team of eight dedicated individuals, they are committed to making significant strides in the field of MPN research.
Official website here: www.mpnresearchfoundation.org
Is The Mpn Research Foundation legitimate?
The Mpn Research Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. The Mpn Research Foundation submitted a form 990, which is a tax form used by tax-exempt organizations in the U.S., indicating its operational transparency and adherence to regulatory requirements. Donations to this organization are tax deductible.
Here are some key statistics you may want to consider:
Executive Compensation: $209,184
Professional Fundraising Fees: $0
Other Salaries and Wages: $763,321
For more financial information, click here
What is the mission statement of The Mpn Research Foundation?
The Mpn Research Foundation's primary mission is to actively promote, finance, and support groundbreaking and effective research aimed at uncovering the causes, treatments, and potentially, a cure for Essential Thrombocythemia (ET), Polycythemia Verra (PV), and Myelofibrosis (MF). The organization's funds are allocated towards research in these specific blood disorders, and it also encourages collaboration within the scientific community to expedite MPN research.
Official website here: www.mpnresearchfoundation.org
Who is the CEO of The Mpn Research Foundation?
Barbara Van Husen is the President of The Mpn Research Foundation. The CEO's salary of The Mpn Research Foundation is $209,184 and their total compensation is $209,184.
Official website here: www.mpnresearchfoundation.org
What is the revenue of The Mpn Research Foundation?
The Mpn Research Foundation's revenue in 2022 was $3,895,930.
Official website here: www.mpnresearchfoundation.org
Who are the executives of The Mpn Research Foundation and what are their salaries?
The average compensation at The Mpn Research Foundation during 2022 was $121,563. There are 8 employees and 14 volunteers at The Mpn Research Foundation.
Here are 15 key members and their salaries (The Mpn Research Foundation's CEO's salary is $209,184 and their total compensation is $209,184):
- Kapila Viges (Chief Executive Officer)
- Barbara Van Husen (President) [Trustee/Director]
- Joann Mason (Secretary) [Trustee/Director]
- David Boule (Treasurer) [Trustee/Director]
- Ed Bartholomey (Director)
- Jen Bealer (Director)
- Stephen Berger (Director)
- Lisa G Bretones (Director)
- Stephanie Cindric (Director)
- Brandon Goetzman (Director)
- Sam Klepper (Director)
- Pam Murphy (Director)
- David Ricci (Director)
- Rebecca Shapiro (Director)
- Jeff Shier (Director)
Official website here: www.mpnresearchfoundation.org
Where can I find the form 990 for The Mpn Research Foundation?
The The Mpn Research Foundation’s most recent form 990 was submitted in 2022 and can be accessed here
Official website here: www.mpnresearchfoundation.org
Learn more at the official website: www.mpnresearchfoundation.org
Mission Statement of The Mpn Research Foundation
The MPN Research Foundation, in its mission, is committed to advocating, financing, and backing research aimed at understanding the root causes, developing effective treatments, and potentially finding a cure for Essential Thrombocythemia (ET), Polycythemia Vera (PV), and Myelofibrosis (MF). This nonprofit organization's primary objective is to promote and support the most cutting-edge and successful research in these areas. Furthermore, The MPN Research Foundation encourages collaboration within the scientific community to accelerate the progress of MPN research. By funding research, this foundation plays a significant role in advancing our understanding of these diseases and bringing us closer to finding effective treatments and potential cures for individuals affected by ET, PV, and MF.
Impact
This information is meant to be a general summary of The Mpn Research Foundation. Please take the time to review official sources before making any decisions based upon the content provided here.
Thursday, August 15, 2024
The MPN Research Foundation is dedicated to promoting, funding, and supporting research into the causes, treatments, and potentially the cure for essential thrombocythemia, polycythemia vera, and primary myelofibrosis. By funding research initiatives and promoting collaboration within the scientific community, the foundation is accelerating progress in understanding and combatting these rare blood cancers. Their impact is felt not only within the medical research field but also in the lives of individuals affected by these diseases, offering hope for improved treatments and ultimately a cure.
Financials
This financial information is from Propublica.
Other financial information:
This information is from the most recently submitted tax form from this organization, which was in 2022.
- Assets and Liabilities:
Organization Details
Founding Year
1999
Phone
(312) 683-7228
Principal Officer
Barbara Van Husen
Main Address
180 N MICHIGAN AVENUE 1870, CHICAGO, IL, 60601
NTEE Category
Code: H50 - Medical research
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