By Barbara Obstoj-Cardwell. Editor
US biotech major Amgen last Monday announced that the US Food and Drug Administration (FDA) will hold an advisory committee (AdCom) meeting to review the supplementary new drug (sNDA) for full approval of its cancer drug Lumakras. US mRNA focused Moderna last week entered into a collaboration with China’s CARsgen Therapeutics to evaluate a CT041 combination as an mRNA cancer vaccine. US biotech start-up Cellares, which calls itself the first “integrated” development and manufacturing organization (IDMO), has secured $255 million in a series C financing. Also, Denmark’s Novo Nordisk last week presented new data extolling the benefits of its obesity management drug Wegovy (semaglutide) for patients with heart failure.
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