USA-based BioCryst Pharmaceuticals says that its partner, South Korea-headquartered Green Cross Corp, has received marketing and manufacturing approval from the Korean Food & Drug Administration (KFDA) for intravenous peramivir to treat patients with influenza A and B viruses, including pandemic H1N1 and avian influenza. Green Cross intends to launch peramivir under the commercial name PeramiFlu in South Korea.
Jon Stonehouse, president and chief executive of BioCryst, commented: 'We are pleased that intravenous peramivir is now approved in Korea and represents the second country this year to make this important treatment option available for patients suffering from seasonal influenza. BioCryst continues to focus on completing the US development of IV peramivir as a potential treatment for hospitalized patients with seasonal influenza.'
Japanese marketing partner Shionogi started selling the product on its domestic market earlier this year, under the trade name Rapiacta.
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 2025 | Headless Content Management with Blaze