Genetic Medicines to Treat Cardiovascular Disease
About This Grant
Abstract Support is requested for a Keystone Symposia conference entitled Genetic Medicines to Treat Cardiovascular Disease, organized by Drs. Rick Dewey, Litsa G. Kranias and James S. Ware, with scientific programming input from Keystone Symposia. The meeting will take place Jan 25–28, 2027 at Keystone Resort in Keystone, Colorado, United States. Genetic medicines are paving the way for groundbreaking treatments in cardiovascular diseases (CVD). With advancements in gene therapy, RNA-based therapies, stem cell research, and gene editing, a growing number of clinical trials are underway. This Keystone Symposia meeting on Genetic Medicines to Treat Cardiovascular Disease will bring together diverse groups of basic scientists, clinicians, and industry professionals to foster meaningful discussions of the exciting opportunities emerging from industry-academia collaborations and partnerships. The sessions will explore cutting-edge advancements in identifying new therapeutic targets, translational research and clinical studies aimed at treating CVD. Topics will include breakthroughs in genetic therapies, as well as challenges related to delivery methods, efficacy, safety and cardiac tissue modeling to better understand disease phenotypes. Additionally, the program will feature panel discussions focused on the steps leading from basic discovery to translation, commercialization, FDA approval, and navigating the venture capital landscape. Other key topics will include long-term and off-target effects of therapies, ethical and regulatory considerations, lessons from preclinical and clinical trials, and professional development challenges for early-career researchers. The sessions will highlight latest scientific discoveries but also will explore their translational impacts and emerging challenges, especially in relation to pre-clinical and clinical trial design and the integration of AI technologies to advance genetic medicines. To achieve this, the conference brings together basic researchers, clinicians and industry partners demonstrating the crucial role that interdisciplinary collaborations play in driving growth in this area. Further, the meeting will be held concurrently with our successful joint Keystone Symposia conferences on Precision Genome Engineering and Nucleic Acid Delivery. By placing these three distinct, but related, meetings at the same venue attendees will have access to a broader cross section of talks and attendees that span the scope of genetic medicine research.
Grant Summary
Genetic Medicines to Treat Cardiovascular Disease is a NHLBI - National Heart Lung and Blood Institute grant providing up to $19K for university, nonprofit, healthcare org. Applications are due 2027-07-31 (open). Check eligibility and apply with FindGrants.
Not quite the right fit?
Search 9,000+ open grants, or get matches ranked for your organization — free.
Focus Areas
Eligibility
How to Apply
Up to $19K
2027-07-31
- 1Confirm your organization is eligible for Genetic Medicines to Treat Cardiovascular Disease from NHLBI - National Heart Lung and Blood Institute, checking organization type, location, and any population or project requirements.
- 2Gather the required documents and information, including your organization details, project plan, and budget figures.
- 3Draft your application narrative and budget addressing the funder's priorities and review criteria. FindGrants can draft each section for you to review and edit.
- 4Review every section against the requirements checklist, then export a submission-ready application pack and submit it to NHLBI - National Heart Lung and Blood Institute before the deadline.
Don't want to draft it yourself?
We'll draft the complete application against NHLBI - National Heart Lung and Blood Institute's requirements, run a quality review, and email you a submission-ready PDF plus an editable Word doc within 5 business days. Most orders deliver in 24-48 hours. Flat $399, any grant size.
AI Requirement Analysis
Detailed requirements not yet analyzed
Have the NOFO? Paste it below for AI-powered requirement analysis.
Genetic Medicines to Treat Cardiovascular Disease: Frequently Asked Questions
Who is eligible for the Genetic Medicines to Treat Cardiovascular Disease?
Genetic Medicines to Treat Cardiovascular Disease is offered by NHLBI - National Heart Lung and Blood Institute and is generally open to university, nonprofit, healthcare org. It is open to organizations nationwide unless the funder specifies otherwise. Review the specific eligibility terms before applying, since funders set their own requirements around organization type, location, and the population or project being served.
How much funding does the Genetic Medicines to Treat Cardiovascular Disease provide?
Genetic Medicines to Treat Cardiovascular Disease provides up to $19K per award from NHLBI - National Heart Lung and Blood Institute. Actual award sizes depend on the scope of your project, available program funds, and the number of applicants, so build a budget that reflects realistic, allowable costs rather than the maximum figure.
When is the Genetic Medicines to Treat Cardiovascular Disease deadline?
Applications for Genetic Medicines to Treat Cardiovascular Disease are due 2027-07-31 (open). Because deadlines can change, verify the date with the funder, NHLBI - National Heart Lung and Blood Institute, and give yourself enough time to prepare a complete, competitive application before the close date.
How do you apply for the Genetic Medicines to Treat Cardiovascular Disease?
To apply for Genetic Medicines to Treat Cardiovascular Disease, confirm your eligibility, gather the required documents, and prepare a narrative and budget that address the funder's priorities. FindGrants guides you step by step and can draft each section, then exports a submission-ready application pack for this grant from NHLBI - National Heart Lung and Blood Institute.