Gilead reports positive data from Phase 3b HIV study of Complera
Data demonstrated that Complera is non-inferior to Atripla, achieving HIV RNA levels less than 50 copies/mL through 48 weeks of therapy, the primary endpoint of the study. On
The US Food and Drug Administration (FDA) has granted rare paediatric disease designation to Vanda Pharmaceuticals’ VCA-894A, an investigational antisense oligonucleotide therapy for Charcot-Marie-Tooth disease, axonal, type 2S (CMT2S).