Drug Discovery RFP
Offered by Families of Spinal Muscular Atrophy · Elk Grove Village, IL
About this opportunity
Cure SMA's drug discovery program converts basic research ideas into new drug candidates for spinal muscular atrophy. The program has invested $20 million in funding for 12 drug development projects that have led to effective treatments for SMA. The continued preclinical drug discovery program funds innovative and promising projects that will lead directly to creating new viable drugs, with investment in both combination and new muscle-targeting therapies.
How to apply
Applications are handled on the funder's own website. Review the full guidelines and apply here: curesma.org/funding-opportunities. Confirm the deadline and eligibility directly with Families of Spinal Muscular Atrophy before applying.
See Families of Spinal Muscular Atrophy's full giving profile — its grant history, top recipients, and other funding priorities.
Is this grant a fit for your nonprofit?
Before you spend hours on an application, know whether it's worth it. Bespoke Grants scores any open RFP against your mission, budget, and service area — and finds the other funders you're missing. Free, no credit card.
Check my fit & find more grants →Other open opportunities from Families of Spinal Muscular Atrophy
Families of Spinal Muscular Atrophy currently lists 2 open opportunities in our index.
- Basic Research RFP
Frequently asked questions
- What is the deadline for Drug Discovery RFP?
- The application deadline is No fixed deadline recorded. Deadlines can change — always confirm directly with Families of Spinal Muscular Atrophy before applying.
- How much funding is available?
- The award amount is not specified by the funder.
- Where do I apply?
- Applications are submitted through Families of Spinal Muscular Atrophy's own website or process — see the "How to apply" section above.