Mylan applauds Drug Safety and Innovation act launch
The Act, which was initiated by US president Barack Obama, enables all drug manufacturers to meet FDA’s inspection standards and improve timely access to affordable generic drugs. Mylan
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).
Under the collaboration agreement between Auxilium and Actelion, Actelion received exclusive rights to commercialize Xiaflex for the treatment of Dupuytren’s contracture and Peyronie’s disease in Canada, Australia, Brazil