Want to stay on top of the science and politics driving biotech today? Sign up to get our biotech newsletter in your inbox.
Hey there. So, today we talk about how Eli Lilly’s gene therapy, developed by Akouos, worked in a child born with an inherited form of deafness. Also, we see some interesting biopharma trends from Stifel, and consider Novo Nordisk’s new obesity investment that is tangential to GLP-1s.
Lilly’s gene therapy restores hearing in a child
A gene therapy made by Eli Lilly has allowed an 11-year-old boy with a genetic form of deafness to hear sound for the first time. Aissam Dam’s inability to hear is caused by a mutation in a single gene, called otoferlin. The gene therapy is delivered directly to the ear, which is a closed system — so it won’t affect other cells in the body. There are about 200,000 people with this form of deafness around the world, the New York Times writes.
To submit a correction request, please visit our Contact Us page.
STAT encourages you to share your voice. We welcome your commentary, criticism, and expertise on our subscriber-only platform, STAT+ Connect