Let’s Chat About…Atsena Therapeutics’ work in LCA

October 27, 2022 @ 1:00PM — 2:00PM Eastern Time (US & Canada) Add to Calendar

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Join our conversation on Atsena Therapeutics’ work in LCA with Shannon Boye and Kara Fick

Let’s Chat About … Atsena Therapeutics’ work in LCA

Join us for an introduction to Atsena Therapeutics with Kara Fick, Head of Patient Advocacy, and Shannon Boye, Founder and Director. We’ll talk about Atsena’s approach to gene therapy and their ongoing work in LCA.

About Kara Fick

Kara is the head of Patient Advocacy and Medical Affairs at Atsena Therapeutics. She has been working as a patient advocate for rare disease in the biotech world for nearly a decade and is passionate about bringing the patient voice, perspective, and expertise to the table. At Atsena, Kara strives to bridge the gap between the science of innovative therapies and the daily needs of individuals living with rare diseases. She also works to better understand the current barriers to diagnosis, treatment, and management of rare disease and ways that we can better address those hurdles with patients and clinicians alike. Kara holds a BS in Biomedical Sciences from Texas A&M University.



About Shannon Boye



Dr. Shannon E. Boye is a Professor and Associate Chief of the Division of Cellular and Molecular Therapy in the University of Florida’s Department of Pediatrics. She received her BS in marine biology with a minor in chemistry from Fairleigh Dickinson University in 2001. She graduated with a PhD in Neuroscience from the University of Florida in 2006. Her thesis work involved developing viral vectors for the treatment of retinal disease, specifically GUCY2D Leber Congenital Amaurosis (LCA1). Dr. Boye has authored over 60 peer-reviewed manuscripts, multiple textbook chapters, is actively involved in grant and manuscript review, and is the recipient of several major awards. Shannon and her husband Sanford are the founders of Atsena Therapeutics.

About the "Let's Chat About..." Web Series

This webinar is part of our continued Let’s Chat About webinar series. We've developed this free, virtual web series with those living with LCA and IRDs in mind, but we invite all members of our community, including those in research, industry, and the regulatory communities to join any of the sessions, as we look ahead to a common goal of advancing treatments for rare retinal disease.
We encourage you to register in advance (it’s always free!), and to let us know what questions you have for our speaker. If you cannot attend the live webinar, you will be able to access the recording from our Let's Chat About... web page here. To view a list of past speakers and topics, or listen to previous sessions, click here.

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