Once hotly-tipped biotech Intarcia Therapeutics has been dealt a bodyblow from the US regulator, with a second rejection for its drug-device combination ITCA-650.
The product is designed to provide a patient-friendly alternative to regular GLP-1 agonist injections for people with diabetes.
The matchstick-sized device is implanted under the skin, delivering a special formulation of exenatide, also marketed as Bydureon and Byetta by AstraZeneca (LSE: AZN), with the aim of delivering a steady six-month supply.
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