
US biotech major Gilead Sciences (Nasdaq: GILD) has expanded its hepatitis C generic licensing agreements to include the investigational NS5A inhibitor GS-5816.
The investigational drug is being evaluated in Phase III clinical studies as part of a single tablet regimen that combines the compound and Sovaldi (sofosbuvir) for the treatment of all six genotypes of hepatitis C. The expanded agreements will allow Gilead’s India-based partners to manufacture GS-5816 and the single tablet regimen of Sovaldi/GS-5816, once approved, for distribution in 91 developing countries, which account for 54% of the worldwide population of individuals infected with the hepatitis C virus (HCV). The Sovaldi/GS-5816 regimen would become the first pan-genotypic, all-oral single tablet regimen for HCV.
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
| Headless Content Management with Blaze