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Grants for Rare Disease Programs is sponsored by Sarepta Therapeutics. Sarepta provides grant funding for programs that enable education, address unmet needs of rare disease patients, promote the highest standards of care, raise awareness of ongoing research, or focus on other critical community initiatives.
Requests are considered across the spectrum of neuromuscular and rare diseases, with priority given to Duchenne muscular dystrophy, limb-girdle muscular dystrophy, and other conditions. [16]
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Or search similar grants →According to the current listing, eligibility includes: Organizations supporting programs that enable education, address unmet needs of rare disease patients, promote the highest standards of care, raise awareness of ongoing research, or focus on other critical community initiatives. [16]. Confirm the full requirements in the official notice before applying.
Applications for Grants for Rare Disease Programs are due November 15, 2026. Build your timeline backwards from this date to cover registrations, approvals, and final submission checks.
Grants for Rare Disease Programs is funded by Sarepta Therapeutics. Verify program details on the funder's official page before applying.
Start from the official opportunity page linked in this listing — it carries the sponsor's submission instructions.
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Grants & Donations (Rare Diseases) is sponsored by Sarepta Therapeutics. Sarepta Therapeutics provides grant funding for programs that enable education, address unmet needs of rare disease patients, promote the highest standards of care, raise awareness of ongoing research, or focus on other critical community initiatives across the spectrum of neuromuscular and rare diseases.
Grants & Donations (Rare Disease Community) is sponsored by Sarepta Therapeutics. Sarepta Therapeutics provides grant funding for programs that enable education, address unmet needs of rare disease patients, promote high standards of care, raise awareness of ongoing research, or focus on other critical community initiatives. Priority is given to Duchenne muscular dystrophy, limb-girdle muscular dystrophy, and other disease areas of focus for the company, but requests are considered across the spectrum of neuromuscular and rare diseases.