PARD Science Award
Funds collaborative retinal disease research within Friedreich ataxia scientific programs.
The PRPH2 and Associated Retinal Diseases (PARD) Science Award is a co-funded program administered jointly by the Foundation Fighting Blindness and the Nixon Visions Foundation. Foundation Fighting Blindness is a US 501(c)(3) public charity established in 1971 that has raised nearly $1 billion supporting retinal disease research. The PARD award is narrowly scoped to PRPH2-related retinal disease: funded projects must advance understanding of PRPH2 biology and pathophysiology in the retina, or work toward potential treatments for PRPH2-associated inherited retinal diseases. Research outside the PRPH2 gene and its direct pathophysiology is not within scope of this award.
Awards reach up to $500,000 over one to three years. The application process is two-stage: applicants first submit a Letter of Intent (LOI) via the Foundation's online portal; only applicants invited on the basis of their LOI submit a full application. For the FY26 cycle, the LOI deadline was 28 August 2025 and the full application deadline was 20 November 2025; that cycle is now fully closed. The FY27 cycle is expected to open in 2026, consistent with the program's annual cadence. PDF LOI guidelines, application guidelines, and a budget template are published on the program page when the cycle opens.
For-profit entities are not eligible for the PARD award; applicants must be non-profit organizations, universities, or research institutions. Because budget terms may carry conditions from both the Foundation Fighting Blindness and the Nixon Visions Foundation, applicants should review guidelines from both co-funders before budgeting. Researchers with strong PRPH2-specific expertise and institutional affiliation should track the program's page from mid-2026 for the FY27 RFP announcement, and should prepare LOI materials in advance given the narrow eligibility window.
Funds meritorious research advancing understanding of PRPH2 biology and pathophysiology in the retina and potential treatments for PRPH2-associated inherited retinal diseases.
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