Bangladeshi generics and active ingredients maker Beximco Pharmaceuticals today announced the launch of the world's first generic version of Pfizer’s (NYSE: PFE) COVID-19 treatment Paxlovid (nirmatrelvir and ritonavir tablets, co-packaged for oral use), which was granted emergency use authorization (EUA) by the US Food and Drug Administration on December 22, 2021.
Bangladesh’s Directorate General of Drug Administration (DGDA) today granted EUA for the oral antiviral drug to treat mild-to-moderate COVID-19 in adults and children of 12 years and above, the company noted.
This novel antiviral pill showed almost 90% efficacy in preventing hospitalizations and deaths in high-risk patients, and recent data from Pfizer suggests the drug retains its effectiveness against the fast-spreading Omicron variant of the coronavirus. Beximco Pharma will market this product under the brand name Bexovid, initially in Bangladesh.
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