The Mark Egly Foundation is dedicated to transforming lives through groundbreaking research in Alpha-1 Antitrypsin science. Our funding priorities reflect both the urgent needs of those currently living with Alpha-1 Antitrypsin Deficiency (AATD) and the emerging potential of AAT therapy to benefit far broader patient populations.
We support research that will:
As our understanding of AAT's therapeutic potential expands and more patients with AATD are diagnosed through improved screening, the global demand for Alpha-1 Antitrypsin therapy is rapidly increasing. We prioritize funding for:
Emerging research reveals that Alpha-1 Antitrypsin's protective and anti-inflammatory properties may benefit numerous conditions previously unrecognized as related to circulating AAT levels. We actively seek to fund researchers investigating:
These expanded therapeutic applications are documented in detail within Mark Egly's patent claims, which outline innovative uses of Alpha-1 Antitrypsin for treating conditions whose relationship to AAT levels was previously unknown or underappreciated by the medical community.
We need visionary researchers who understand the critical importance of:
Projects focused on:
Studies examining:
The Mark Egly Foundation seeks research proposals that demonstrate:
We encourage researchers to think expansively about Alpha-1 Antitrypsin's potential. Mark Egly's pioneering work demonstrated that AAT's protective mechanisms extend far beyond lung and liver disease. We welcome proposals that:
Our funding may support:
The Mark Egly Foundation is committed to:
The research we fund today will define the treatments available tomorrow. By supporting innovative, high-impact projects that expand both the production and therapeutic applications of Alpha-1 Antitrypsin, we honor Mark Egly's legacy while advancing hope for millions of patients worldwide.
For information about grant opportunities, application procedures, and funding cycles, please visit our Grant Opportunities page or contact our research program team.