A fairly positive outcome from a meeting of the US regulator’s scientific panel raises the prospect that pharma major GSK (LSE: GSK) may be able to succeed where its British counterpart AstraZeneca (LSE: AZN) has failed.
The firm is developing daprodustat, a novel kind of oral therapy, as an option for the treatment of anemia associated with chronic kidney disease (CKD).
Mindful of the safety risks associated with these drugs, known as hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHI), the Food and Drug Administration's (FDA) scientists have previously voted against approving options from AstraZeneca and Akebia Therapeutics (Nasdaq: AKBA).
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