Russia seeks to legitimize Sputnik V

moscow-big

Given the lack of Phase III data, it is not surprising that some international media reports reacted with skepticism to Russia’s approval of the so-called Sputnik V vaccine for COVID-19 last week.

So the experts lined up to give a media briefing on the vaccine on Thursday focused on irrefutable evidence showing human adenovirus-based drugs to be safe and effective, and on the experience of Moscow's Gamaleya Research Institute of Epidemiology and Microbiology in using this technology.

The center has been working on adenoviral vector-based vaccines since the 1980s and produced one against Ebola and another – albeit unapproved – against Middle East Respiratory Syndrome (MERS).

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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

Today's issue

Company Spotlight





More Features in Pharmaceutical