Amanda Moore | VP, Program Leadership & Clinical Operations
Abeona Therapeutics

Amanda Moore, VP, Program Leadership & Clinical Operations, Abeona Therapeutics

Over the past 20+ years, Amanda Moore has had the pleasure of gaining depth and breadth of experience in multiple roles across clinical development operations, program leadership, and research.  She has led cross-functional programs and contributed to development activities of four approved and marketed products across multiple therapeutic areas, including two gene therapies and two first in class treatments. With almost 25 years of experience beginning in basic research labs and expanding into site and CRO expertise, she has a solid foundation on which she has built strong development programs in the biotechnology and pharmaceutical industry with a track record of leading innovation in clinical trials, pioneering operating committee relationships, building high-functioning teams, and oversight of global development programs.  Her experience spans the development lifecycle and includes rare disease, gene and cell therapy, and both small and large molecule development.  Ms Moore holds a master’s degree in Health Science from the George Washington University.

Appearances:



Day 1 - World Orphan Drug Congress USA 2026 @ 15:10

Mindset Matters in Designing and Operationalizing Clinical Trials for Rare

  • An open and innovative mindset is the key to ensuring clinical trial designs are optimized for patient participation and results-driven clinical trial 
  • Many tools and approaches exist for rare disease clinical development, and it is the disease-informed and creative application of those tools and approaches that paves the pathway for success 
  • Abeona’s clinical trials for patients with Recessive Dystrophic Epidermolysis Bullosa (RDEB) provide several examples of the application of this mindset with the approval of our gene therapy in 2025 
last published: 06/Feb/26 15:55 GMT

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