GSK to open new global vaccines R&D center in Maryland, US
Up to 200 new jobs will be created at the Rockville facility, with GSK investing over $50m in the next two years to continue to develop the site
The US Food and Drug Administration (FDA) has accepted for review the supplemental biologics license application (sBLA) for Sanofi and Regeneron’s Dupixent (dupilumab) to treat chronic spontaneous urticaria (CSU) in adults and children aged 12 and above, particularly for those whose condition persists despite H1 antihistamine treatment.