PTAC Research Grant supports independent investigators’ basic research into restoring CFTR function or repairing or replacing the defective gene to inform therapies for people with cystic fibrosis.
Funder: Cystic Fibrosis Foundation
Due Dates (Anticipated): May 2027 (Full application deadline)
Funding Amounts: Up to $150,000 per year, plus up to 12% indirect costs, for up to two years
Summary: Supports basic research that could advance therapies to restore CFTR function or repair or replace the defective CFTR gene.
Key Information: Applicants must be independent investigators; projects must address a Path to a Cure research area.
The Cystic Fibrosis Foundation’s Path to a Cure (PTAC) Research Grant supports basic science that could inform therapies for people with cystic fibrosis whose CFTR variants are not served by existing small-molecule modulators. Projects may investigate foundational concepts, strategies, tools or technologies to restore CFTR protein function or repair or replace the defective gene. Proposals generally must be hypothesis-driven and supported by sufficient preliminary data, although development of useful tools or reagents may also be considered.
Priority topics include airway and submucosal-gland cells, nonsense-mutation readthrough, gene insertion, targeted delivery of nucleic acid therapies, delivery of large gene-editing components, immune responses to genetic therapies, and in vitro assays of CFTR restoration. Work centered on infection, airway hydration or non-lung manifestations belongs in the foundation’s general Research Award program.