NewLink Genetics (Nasdaq: NLNK) says that partner US pharma giant Merck & Co (NYSE: MRK) has reached two key regulatory milestones for the Ebola Zaire vaccine candidate known as V920 (rVSV∆G-ZEBOV-GP).
The US Food and Drug Administration has granted the vaccine candidate Breakthrough Therapy designation, and the European Medicines Agency provided the vaccine candidate PRIME (PRIority MEdicines) status.
The news lifted NewLink’s shares 1.3% to $11.17 by close of trading and a further 1.6% to $11.17 in post-market trading on Monday.
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