Gilead Sciences International Ltd.'s new two-drug fixed-dose HIV therapy Descovy, containing the new tenofovir prodrug tenofovir alafenamide (TAF) and emtricitabine, has received a positive opinion from Europe's top scientific advisory panel, the Committee for Medicinal Products for Human Use (CHMP), the company announced Feb. 26; Descovy is expected to be approved by the European Commission in two to three months.
Tenofovir alafenamide has exhibited high antiviral efficacy similar to and at a dose of less than one-tenth of its marketed...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?