Cempra Pharma Completes Phase 1 Studies For CEM-101
According to Cempra Pharma, CEM-101 is expected to be the first macrolide to have an intravenous formulation available in the US since intravenous azithromycin was approved in 1997,
ReviR Therapeutics has received a rare paediatric disease designation (RPDD) from the US Food and Drug Administration (FDA) for RTX-117, its investigational oral small-molecule therapy for Charcot-Marie-Tooth disease (CMT).