Gilead Submits sNDA for Truvada
According to the company, Truvada once approved would be the first agent indicated for uninfected individuals to reduce the risk of acquiring HIV through sex, a prevention approach
Kyowa Kirin subsidiary Kyowa Kirin EMEA has received approval from the European Commission (EC) to expand the use of Crysvita (burosumab) for treating X-linked hypophosphataemia (XLH) in infants aged one month to one year across the EU and European Economic Area.
Enlight emphasizes on areas including molecular imaging, biologics, drug formulation delivery methods, besides novel chemistries, production technologies, biomarkers and drug safety. Enlight CEO Michelle Browner said the company
Belimumab belongs to a class of drugs known as BLyS-specific inhibitors. The multi-center, international, randomized, double-blind, placebo-controlled, 52-week study will investigate use of belimumab administered subcutaneously (SC) once-weekly