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Readthrough Therapies for RYR-1-Related Disease Due to Nonsense Variants Research Grant Awards
Targeted Request for Grant Application
Deadline: May 1, 2026
The RYR-1 Foundation is pleased to invite investigators to submit a Request for Proposal (RFP) focused on the following Research Priority Area (RPA)
- Readthrough Therapies for RYR-1-Related Disease (RYR-1-RD) due to Nonsense Variants
- This RPA is the focus of this RFP for the following reasons: 1) The clinical severity of RYR-1-RD patients with nonsense variants, 2) The ongoing development of a nonsense RYR-1-RD mouse model (see details below), and 3) The growing field of readthrough therapies, including both small molecules and tRNA-based therapies.
Summary of Application Format:
- Title Page (Project Title) of the RYR-1-Related Diseases (RYR-1-RD) Project
- Enable Other Users to Access this Proposal
- Information/Acknowledgements
- Applicant/PI
- Institution & Contacts
- Key Personnel (including a short curriculum vitae or NIH Biosketch)
- Abstract
- Impact Statement
- Preliminary/Supporting Data
- Budget Period Detail
- Budget Summary and Justification
- Organization Assurances
- Attachments
- Signature Page
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