In Cambridge, USA, just around the corner from fellow gene therapy specialist bluebird bio (Nasdaq: BLUE), a less well-known biotech startup could be about to shake up the market for certain rare disease therapies.
Like bluebird, Avrobio (Nasdaq: AVRO) is pursuing an ex vivo technique, genetically modifying a person’s own bone marrow cells to deliver novel, healthy genes to people suffering from very rare and very serious inherited disorders.
While the firm has not been in the limelight as much as its more famous neighbor, a recent positive data update could help to change that.
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
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze