ViroPharma has applied to the US Food and Drug Administration forapproval to market Picovir (pleconaril), its antiviral intended as a treatment for adults with viral respiratory infections (colds) caused by picornaviruses. The filing is a major achievement for the drug, which was all but written off last year after it achieved disappointing results in three successive clinical trials (Marketletter April 17, 2000)
Earlier this year, the company reported positive results from two Phase III trials of the drug, which showed that it had an effect on symptoms within 24 hours and reduced by approximately one day the time to resolution of symptoms (Marketletter March 26). Additional studies are planned looking at the drug's use in children and in the prevention of colds.
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