
US biotech start-up Aurora Therapeutics has launched with $16 million in seed funding from Menlo Ventures, aiming to turn one-off CRISPR gene-editing successes into a scalable model for rare diseases. The company argues that recent regulatory shifts and technical advances have finally lowered long-standing barriers.
Menlo Ventures incubated Aurora to tackle a core problem in rare disease genetics: most conditions involve hundreds or thousands of mutations, many too uncommon to justify conventional clinical development. Aurora says its platform can treat common and ultra-rare mutations in parallel under a unified strategy.
Edward Kaye has been appointed chief executive. Aurora was founded by Jennifer Doudna and Fyodor Urnov, building on work that includes the first bespoke CRISPR therapy used to treat an infant with CPS1 deficiency.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
| Headless Content Management with Blaze